A powerful central nervous system stimulant and sympathomimetic. Amphetamine has multiple mechanisms of action including blocking uptake of adrenergics and dopamine, stimulation of release of monamines, and inhibiting monoamine oxidase. Amphetamine is also a drug of abuse and a psychotomimetic. The l- and the d,l-forms are included here. The l-form has less central nervous system activity but stronger cardiovascular effects. The d-form is DEXTROAMPHETAMINE.
Analogs or derivatives of AMPHETAMINE. Many are sympathomimetics and central nervous system stimulators causing excitation, vasopressin, bronchodilation, and to varying degrees, anorexia, analepsis, nasal decongestion, and some smooth muscle relaxation.
A loosely defined group of drugs that tend to increase behavioral alertness, agitation, or excitation. They work by a variety of mechanisms, but usually not by direct excitation of neurons. The many drugs that have such actions as side effects to their main therapeutic use are not included here.
The d-form of AMPHETAMINE. It is a central nervous system stimulant and a sympathomimetic. It has also been used in the treatment of narcolepsy and of attention deficit disorders and hyperactivity in children. Dextroamphetamine has multiple mechanisms of action including blocking uptake of adrenergics and dopamine, stimulating release of monamines, and inhibiting monoamine oxidase. It is also a drug of abuse and a psychotomimetic.
Disorders related or resulting from use of amphetamines.
A central nervous system stimulant and sympathomimetic with actions and uses similar to DEXTROAMPHETAMINE. The smokable form is a drug of abuse and is referred to as crank, crystal, crystal meth, ice, and speed.
Detection of drugs that have been abused, overused, or misused, including legal and illegal drugs. Urine screening is the usual method of detection.
An N-substituted amphetamine analog. It is a widely abused drug classified as a hallucinogen and causes marked, long-lasting changes in brain serotonergic systems. It is commonly referred to as MDMA or ecstasy.
One of the catecholamine NEUROTRANSMITTERS in the brain. It is derived from TYROSINE and is the precursor to NOREPINEPHRINE and EPINEPHRINE. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (RECEPTORS, DOPAMINE) mediate its action.
Relatively invariant mode of behavior elicited or determined by a particular situation; may be verbal, postural, or expressive.
An amphetamine derivative that inhibits uptake of catecholamine neurotransmitters. It is a hallucinogen. It is less toxic than its methylated derivative but in sufficient doses may still destroy serotonergic neurons and has been used for that purpose experimentally.
Collection of pleomorphic cells in the caudal part of the anterior horn of the LATERAL VENTRICLE, in the region of the OLFACTORY TUBERCLE, lying between the head of the CAUDATE NUCLEUS and the ANTERIOR PERFORATED SUBSTANCE. It is part of the so-called VENTRAL STRIATUM, a composite structure considered part of the BASAL GANGLIA.
Any drugs that are used for their effects on dopamine receptors, on the life cycle of dopamine, or on the survival of dopaminergic neurons.
The physical activity of a human or an animal as a behavioral phenomenon.
The observable response an animal makes to any situation.
A microanalytical technique combining mass spectrometry and gas chromatography for the qualitative as well as quantitative determinations of compounds.
Drugs that block the transport of DOPAMINE into axon terminals or into storage vesicles within terminals. Most of the ADRENERGIC UPTAKE INHIBITORS also inhibit dopamine uptake.
Drugs obtained and often manufactured illegally for the subjective effects they are said to produce. They are often distributed in urban areas, but are also available in suburban and rural areas, and tend to be grossly impure and may cause unexpected toxicity.
Drugs designed and synthesized, often for illegal street use, by modification of existing drug structures (e.g., amphetamines). Of special interest are MPTP (a reverse ester of meperidine), MDA (3,4-methylenedioxyamphetamine), and MDMA (3,4-methylenedioxymethamphetamine). Many drugs act on the aminergic system, the physiologically active biogenic amines.
Agents that are used to suppress appetite.
An alkaloid ester extracted from the leaves of plants including coca. It is a local anesthetic and vasoconstrictor and is clinically used for that purpose, particularly in the eye, ear, nose, and throat. It also has powerful central nervous system effects similar to the amphetamines and is a drug of abuse. Cocaine, like amphetamines, acts by multiple mechanisms on brain catecholaminergic neurons; the mechanism of its reinforcing effects is thought to involve inhibition of dopamine uptake.
Sodium chloride-dependent neurotransmitter symporters located primarily on the PLASMA MEMBRANE of dopaminergic neurons. They remove DOPAMINE from the EXTRACELLULAR SPACE by high affinity reuptake into PRESYNAPTIC TERMINALS and are the target of DOPAMINE UPTAKE INHIBITORS.
A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company.
Striped GRAY MATTER and WHITE MATTER consisting of the NEOSTRIATUM and paleostriatum (GLOBUS PALLIDUS). It is located in front of and lateral to the THALAMUS in each cerebral hemisphere. The gray substance is made up of the CAUDATE NUCLEUS and the lentiform nucleus (the latter consisting of the GLOBUS PALLIDUS and PUTAMEN). The WHITE MATTER is the INTERNAL CAPSULE.
Drugs capable of inducing illusions, hallucinations, delusions, paranoid ideations, and other alterations of mood and thinking. Despite the name, the feature that distinguishes these agents from other classes of drugs is their capacity to induce states of altered perception, thought, and feeling that are not experienced otherwise.
An immunoenzyme test for the presence of drugs and other substances in urine and blood. The test uses enzyme linked antibodies that react only with the particular drug for which the sample is being tested.
The application of medical knowledge to questions of law.
A central nervous system stimulant used most commonly in the treatment of ATTENTION DEFICIT DISORDER in children and for NARCOLEPSY. Its mechanisms appear to be similar to those of DEXTROAMPHETAMINE. The d-isomer of this drug is referred to as DEXMETHYLPHENIDATE HYDROCHLORIDE.
The relationship between the dose of an administered drug and the response of the organism to the drug.
Chlorinated analog of AMPHETAMINE. Potent neurotoxin that causes release and eventually depletion of serotonin in the CNS. It is used as a research tool.
Drugs that block the transport of adrenergic transmitters into axon terminals or into storage vesicles within terminals. The tricyclic antidepressants (ANTIDEPRESSIVE AGENTS, TRICYCLIC) and amphetamines are among the therapeutically important drugs that may act via inhibition of adrenergic transport. Many of these drugs also block transport of serotonin.
Drugs that bind to and activate dopamine receptors.
A group of compounds that are methyl derivatives of the amino acid TYROSINE.
The phylogenetically newer part of the CORPUS STRIATUM consisting of the CAUDATE NUCLEUS and PUTAMEN. It is often called simply the striatum.
A technique for measuring extracellular concentrations of substances in tissues, usually in vivo, by means of a small probe equipped with a semipermeable membrane. Substances may also be introduced into the extracellular space through the membrane.
A sympathomimetic drug used primarily as an appetite depressant. Its actions and mechanisms are similar to DEXTROAMPHETAMINE.
Drugs that bind to but do not activate DOPAMINE RECEPTORS, thereby blocking the actions of dopamine or exogenous agonists. Many drugs used in the treatment of psychotic disorders (ANTIPSYCHOTIC AGENTS) are dopamine antagonists, although their therapeutic effects may be due to long-term adjustments of the brain rather than to the acute effects of blocking dopamine receptors. Dopamine antagonists have been used for several other clinical purposes including as ANTIEMETICS, in the treatment of Tourette syndrome, and for hiccup. Dopamine receptor blockade is associated with NEUROLEPTIC MALIGNANT SYNDROME.
An isoquinoline derivative that prevents dopamine reuptake into synaptosomes. The maleate was formerly used in the treatment of depression. It was withdrawn worldwide in 1986 due to the risk of acute hemolytic anemia with intravascular hemolysis resulting from its use. In some cases, renal failure also developed. (From Martindale, The Extra Pharmacopoeia, 30th ed, p266)
Compounds with a five-membered heterocyclic ring with two nitrogens and a keto OXYGEN. Some are inhibitors of TNF-ALPHA production.
A subfamily of G-PROTEIN-COUPLED RECEPTORS that bind the neurotransmitter DOPAMINE and modulate its effects. D2-class receptor genes contain INTRONS, and the receptors inhibit ADENYLYL CYCLASES.
A phenethylamine found in EPHEDRA SINICA. PSEUDOEPHEDRINE is an isomer. It is an alpha- and beta-adrenergic agonist that may also enhance release of norepinephrine. It has been used for asthma, heart failure, rhinitis, and urinary incontinence, and for its central nervous system stimulatory effects in the treatment of narcolepsy and depression. It has become less extensively used with the advent of more selective agonists.
A centrally active drug that apparently both blocks serotonin uptake and provokes transport-mediated serotonin release.
Psychotic organic mental disorders resulting from the toxic effect of drugs and chemicals or other harmful substance.
A sympathomimetic agent with properties similar to DEXTROAMPHETAMINE. It is used in the treatment of obesity. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1222)
Learning situations in which the sequence responses of the subject are instrumental in producing reinforcement. When the correct response occurs, which involves the selection from among a repertoire of responses, the subject is immediately reinforced.
Physiological and psychological symptoms associated with withdrawal from the use of a drug after prolonged administration or habituation. The concept includes withdrawal from smoking or drinking, as well as withdrawal from an administered drug.
An object or a situation that can serve to reinforce a response, to satisfy a motive, or to afford pleasure.
Elongated gray mass of the neostriatum located adjacent to the lateral ventricle of the brain.
Excessive movement of muscles of the body as a whole, which may be associated with organic or psychological disorders.
A region in the MESENCEPHALON which is dorsomedial to the SUBSTANTIA NIGRA and ventral to the RED NUCLEUS. The mesocortical and mesolimbic dopaminergic systems originate here, including an important projection to the NUCLEUS ACCUMBENS. Overactivity of the cells in this area has been suspected to contribute to the positive symptoms of SCHIZOPHRENIA.
Disorders related to substance abuse.
An inhibitor of the enzyme TYROSINE 3-MONOOXYGENASE, and consequently of the synthesis of catecholamines. It is used to control the symptoms of excessive sympathetic stimulation in patients with PHEOCHROMOCYTOMA. (Martindale, The Extra Pharmacopoeia, 30th ed)
Drugs used for their effects on serotonergic systems. Among these are drugs that affect serotonin receptors, the life cycle of serotonin, and the survival of serotonergic neurons.
A group of compounds that are derivatives of beta- aminoethylbenzene which is structurally and pharmacologically related to amphetamine. (From Merck Index, 11th ed)
A derivative of morphine that is a dopamine D2 agonist. It is a powerful emetic and has been used for that effect in acute poisoning. It has also been used in the diagnosis and treatment of parkinsonism, but its adverse effects limit its use.
The action of a drug that may affect the activity, metabolism, or toxicity of another drug.
Cell surface proteins that bind biogenic amines with high affinity and regulate intracellular signals which influence the behavior of cells. Biogenic amine is a chemically imprecise term which, by convention, includes the catecholamines epinephrine, norepinephrine, and dopamine, the indoleamine serotonin, the imidazolamine histamine, and compounds closely related to each of these.
A sympathomimetic that acts mainly by causing release of NOREPINEPHRINE but also has direct agonist activity at some adrenergic receptors. It is most commonly used as a nasal vasoconstrictor and an appetite depressant.
A biochemical messenger and regulator, synthesized from the essential amino acid L-TRYPTOPHAN. In humans it is found primarily in the central nervous system, gastrointestinal tract, and blood platelets. Serotonin mediates several important physiological functions including neurotransmission, gastrointestinal motility, hemostasis, and cardiovascular integrity. Multiple receptor families (RECEPTORS, SEROTONIN) explain the broad physiological actions and distribution of this biochemical mediator.
A substituted benzamide that has antipsychotic properties. It is a dopamine D2 receptor (see RECEPTORS, DOPAMINE D2) antagonist.
Administration of a drug or chemical by the individual under the direction of a physician. It includes administration clinically or experimentally, by human or animal.
Drugs that act on adrenergic receptors or affect the life cycle of adrenergic transmitters. Included here are adrenergic agonists and antagonists and agents that affect the synthesis, storage, uptake, metabolism, or release of adrenergic transmitters.
A class of chemicals derived from barbituric acid or thiobarbituric acid. Many of these are GABA MODULATORS used as HYPNOTICS AND SEDATIVES, as ANESTHETICS, or as ANTICONVULSANTS.
An outbred strain of rats developed in 1915 by crossing several Wistar Institute white females with a wild gray male. Inbred strains have been derived from this original outbred strain, including Long-Evans cinnamon rats (RATS, INBRED LEC) and Otsuka-Long-Evans-Tokushima Fatty rats (RATS, INBRED OLETF), which are models for Wilson's disease and non-insulin dependent diabetes mellitus, respectively.
An alkaloid found in the roots of Rauwolfia serpentina and R. vomitoria. Reserpine inhibits the uptake of norepinephrine into storage vesicles resulting in depletion of catecholamines and serotonin from central and peripheral axon terminals. It has been used as an antihypertensive and an antipsychotic as well as a research tool, but its adverse effects limit its clinical use.
A monoamine oxidase inhibitor with antihypertensive properties.
An organophosphorus cholinesterase inhibitor that is used as an insecticide and an acaricide.
A filament-like structure consisting of a shaft which projects to the surface of the SKIN from a root which is softer than the shaft and lodges in the cavity of a HAIR FOLLICLE. It is found on most surfaces of the body.
A loosely defined grouping of drugs that have effects on psychological function. Here the psychotropic agents include the antidepressive agents, hallucinogens, and tranquilizing agents (including the antipsychotics and anti-anxiety agents).
Fluoroimmunoassay where detection of the hapten-antibody reaction is based on measurement of the increased polarization of fluorescence-labeled hapten when it is combined with antibody. The assay is very useful for the measurement of small haptenic antigens such as drugs at low concentrations.
A complex involuntary response to an unexpected strong stimulus usually auditory in nature.
The ratio of the density of a material to the density of some standard material, such as water or air, at a specified temperature.
Movement or the ability to move from one place or another. It can refer to humans, vertebrate or invertebrate animals, and microorganisms.
A selective, irreversible inhibitor of Type B monoamine oxidase. It is used in newly diagnosed patients with Parkinson's disease. It may slow progression of the clinical disease and delay the requirement for levodopa therapy. It also may be given with levodopa upon onset of disability. (From AMA Drug Evaluations Annual, 1994, p385) The compound without isomeric designation is Deprenyl.
Forceful administration into the peritoneal cavity of liquid medication, nutrient, or other fluid through a hollow needle piercing the abdominal wall.
A subfamily of G-PROTEIN-COUPLED RECEPTORS that bind the neurotransmitter DOPAMINE and modulate its effects. D1-class receptor genes lack INTRONS, and the receptors stimulate ADENYLYL CYCLASES.
Cell-surface proteins that bind dopamine with high affinity and trigger intracellular changes influencing the behavior of cells.
Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters.
A dopamine D2/D3 receptor agonist.
An indirect sympathomimetic. Tyramine does not directly activate adrenergic receptors, but it can serve as a substrate for adrenergic uptake systems and monoamine oxidase so it prolongs the actions of adrenergic transmitters. It also provokes transmitter release from adrenergic terminals. Tyramine may be a neurotransmitter in some invertebrate nervous systems.
Biogenic amines having only one amine moiety. Included in this group are all natural monoamines formed by the enzymatic decarboxylation of natural amino acids.
The tendency to explore or investigate a novel environment. It is considered a motivation not clearly distinguishable from curiosity.
A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automatic behaviors and AMNESIA. CATAPLEXY; SLEEP PARALYSIS, and hypnagogic HALLUCINATIONS frequently accompany narcolepsy. The pathophysiology of this disorder includes sleep-onset rapid eye movement (REM) sleep, which normally follows stage III or IV sleep. (From Neurology 1998 Feb;50(2 Suppl 1):S2-S7)
A general term referring to the learning of some particular response.
Learning that takes place when a conditioned stimulus is paired with an unconditioned stimulus.
The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
A chemically heterogeneous group of drugs that have in common the ability to block oxidative deamination of naturally occurring monoamines. (From Gilman, et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p414)
A hallucinogen formerly used as a veterinary anesthetic, and briefly as a general anesthetic for humans. Phencyclidine is similar to KETAMINE in structure and in many of its effects. Like ketamine, it can produce a dissociative state. It exerts its pharmacological action through inhibition of NMDA receptors (RECEPTORS, N-METHYL-D-ASPARTATE). As a drug of abuse, it is known as PCP and Angel Dust.
Amides of salicylic acid.
A technique using antibodies for identifying or quantifying a substance. Usually the substance being studied serves as antigen both in antibody production and in measurement of antibody by the test substance.
An exaggerated feeling of physical and emotional well-being not consonant with apparent stimuli or events; usually of psychologic origin, but also seen in organic brain disease and toxic states.
A central nervous system stimulant and sympathomimetic with actions and uses similar to those of DEXTROAMPHETAMINE. It has been used most frequently in the treatment of obesity.
A schedule prescribing when the subject is to be reinforced or rewarded in terms of temporal interval in psychological experiments. The schedule may be continuous or intermittent.
A condition characterized by inactivity, decreased responsiveness to stimuli, and a tendency to maintain an immobile posture. The limbs tend to remain in whatever position they are placed (waxy flexibility). Catalepsy may be associated with PSYCHOTIC DISORDERS (e.g., SCHIZOPHRENIA, CATATONIC), nervous system drug toxicity, and other conditions.
The largest and most lateral of the BASAL GANGLIA lying between the lateral medullary lamina of the GLOBUS PALLIDUS and the EXTERNAL CAPSULE. It is part of the neostriatum and forms part of the LENTIFORM NUCLEUS along with the GLOBUS PALLIDUS.
Agents that induce NARCOSIS. Narcotics include agents that cause somnolence or induced sleep (STUPOR); natural or synthetic derivatives of OPIUM or MORPHINE or any substance that has such effects. They are potent inducers of ANALGESIA and OPIOID-RELATED DISORDERS.
Disorders related or resulting from use of cocaine.
A group of naturally occurring amines derived by enzymatic decarboxylation of the natural amino acids. Many have powerful physiological effects (e.g., histamine, serotonin, epinephrine, tyramine). Those derived from aromatic amino acids, and also their synthetic analogs (e.g., amphetamine), are of use in pharmacology.
A propylamine formed from the cyclization of the side chain of amphetamine. This monoamine oxidase inhibitor is effective in the treatment of major depression, dysthymic disorder, and atypical depression. It also is useful in panic and phobic disorders. (From AMA Drug Evaluations Annual, 1994, p311)
A phenyl-piperidinyl-butyrophenone that is used primarily to treat SCHIZOPHRENIA and other PSYCHOSES. It is also used in schizoaffective disorder, DELUSIONAL DISORDERS, ballism, and TOURETTE SYNDROME (a drug of choice) and occasionally as adjunctive therapy in INTELLECTUAL DISABILITY and the chorea of HUNTINGTON DISEASE. It is a potent antiemetic and is used in the treatment of intractable HICCUPS. (From AMA Drug Evaluations Annual, 1994, p279)
A statistical technique that isolates and assesses the contributions of categorical independent variables to variation in the mean of a continuous dependent variable.
Elements of limited time intervals, contributing to particular results or situations.
An involuntary deep INHALATION with the MOUTH open, often accompanied by the act of stretching.
Hallucinogenic alkaloid isolated from the flowering heads (peyote) of Lophophora (formerly Anhalonium) williamsii, a Mexican cactus used in Indian religious rites and as an experimental psychotomimetic. Among its cellular effects are agonist actions at some types of serotonin receptors. It has no accepted therapeutic uses although it is legal for religious use by members of the Native American Church.
A deaminated metabolite of LEVODOPA.
A drug formerly used in the treatment of angina pectoris but superseded by less hazardous drugs. Prenylamine depletes myocardial catecholamine stores and has some calcium channel blocking activity. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1406)
An ergot derivative that acts as an agonist at dopamine D2 receptors (DOPAMINE AGONISTS). It may also act as an antagonist at dopamine D1 receptors, and as an agonist at some serotonin receptors (SEROTONIN RECEPTOR AGONISTS).
Sodium chloride-dependent neurotransmitter symporters located primarily on the PLASMA MEMBRANE of noradrenergic neurons. They remove NOREPINEPHRINE from the EXTRACELLULAR SPACE by high affinity reuptake into PRESYNAPTIC TERMINALS. It regulates signal amplitude and duration at noradrenergic synapses and is the target of ADRENERGIC UPTAKE INHIBITORS.
A plant genus of the family CELASTRACEAE. The leafy stems of khat are chewed by some individuals for stimulating effect. Members contain ((+)-norpseudoephedrine), cathionine, cathedulin, cathinine & cathidine.
The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM.

N-oxygenation of amphetamine and methamphetamine by the human flavin-containing monooxygenase (form 3): role in bioactivation and detoxication. (1/566)

(+)- And (-)-amphetamine and methamphetamine were N-oxygenated by the cDNA expressed adult human flavin-containing monooxygenase form 3 (FMO3), their corresponding hydroxylamines. Two major polymorphic forms of human FMO3 were studied, and the results suggested preferential N-oxygenation by only one of the two enzymes. Chemically synthesized (+/-)-amphetamine hydroxylamine was also a substrate for the human FMO3 and it was converted to phenylpropanone oxime with a stereoselectivity ratio of trans/cis of 5:1. Human FMO3 also N-oxygenated methamphetamine to produce methamphetamine hydroxylamine. Methamphetamine hydroxylamine was also N-oxygenated by human FMO3, and the ultimate product observed was phenylpropanone. For amphetamine hydroxylamine, studies of the biochemical mechanism of product formation were consistent with the production of an N, N-dioxygenated intermediate that lead to phenylpropanone oxime. This was supported by the observation that alpha-deutero (+/-)-amphetamine hydroxylamine gave an inverse kinetic isotope effect on product formation in the presence of human FMO3. For methamphetamine, the data were consistent with a mechanism of human FMO3-mediated N,N-dioxygenation but the immediate product, a nitrone, rapidly hydrolyzed to phenylpropanone. The pharmacological activity of amphetamine hydroxylamine, phenylpropanone oxime, and methamphetamine hydroxylamine were examined for effects at the human dopamine, serotonin, and norepinephrine transporters. Amphetamine hydroxylamine and methamphetamine hydroxylamine were apparent substrates for the human biogenic amine transporters but phenylpropanone oxime was not. Presumably, phenylpropanone oxime or nitrone formation from amphetamine and methamphetamine, respectively, represents a detoxication process. Because of the potential toxic nature of amphetamine hydroxylamine and methamphetamine hydroxylamine metabolites and the polymorphic nature of N-oxygenation, human FMO3-mediated metabolism of amphetamine or methamphetamine may have clinical consequences.  (+info)

Electrophysiological examination of the effects of sustained flibanserin administration on serotonin receptors in rat brain. (2/566)

5-HT1A receptor agonists have proven to be effective antidepressant medications, however they suffer from a significant therapeutic lag before depressive symptoms abate. Flibanserin is a 5-HT1A receptor agonist and 5-HT2A receptor antagonist developed to possibly induce a more rapid onset of antidepressant action through its preferential postsynaptic 5-HT1A receptor agonism. Flibanserin antagonized the effect of microiontophoretically-applied DOI in the medial prefrontal cortex (mPFC) following 2 days of administration, indicating antagonism of postsynaptic 5-HT2A receptors. This reduction in the effect of locally-applied DOI was no longer present following 7-day flibanserin administration. Two-day flibanserin administration only marginally reduced the firing activity of dorsal raphe (DRN) 5-HT neurons. Following 7 days of administration, 5-HT neuronal firing activity had returned to normal and the somatodendritic 5-HT1A autoreceptors were desensitized. The responsiveness of postsynaptic 5-HT1A receptors located on CA3 hippocampus pyramidal neurons and mPFC neurons, examined using microiontophoretically-applied 5-HT and gepirone, was unchanged following a 7-day flibanserin treatment. As demonstrated by the ability of the 5-HT1A receptor antagonist WAY 100635 to selectively increase the firing of hippocampal neurons in 2- and 7-day treated rats, flibanserin enhanced the tonic activation of postsynaptic 5-HT1A receptors in this brain region. The results suggest that flibanserin could be a therapeutically useful compound putatively endowed with a more rapid onset of antidepressant action.  (+info)

Dose linearity study of selegiline pharmacokinetics after oral administration: evidence for strong drug interaction with female sex steroids. (3/566)

AIMS: The purpose of this study was to characterize the dose relationship of selegline and desmethylselegiline pharmacokinetics within the selegiline dose range from 5 to 40 mg. METHODS: Eight female subjects, of whom four were using oral contraceptives, ingested a single dose of 5 mg, 10 mg, 20 mg or 40 mg of selegiline HCl in an open four-period randomized study. Concentrations of selegiline and desmethlylselegiline in serum were measured by gas chromatography for 5 h. As it became evident that the use of oral steroids had a drastic effect on selegiline concentrations, the pharmacokinetic analyses were performed separately for oral contraceptive users and those not receiving any concomitant medication. RESULTS: The total AUC and Cmax of selegiline were 10-to 20-fold higher in those subjects taking oral steroids compared with subjects with no concomitant medication; this finding was consistent and statistically significant at all the four dose levels. The dose linearity of selegiline pharmacokinetics failed to be demonstrated in both groups. The AUC and Cmax of desmethylselegiline were only moderately higher (about 1.5-fold; P=NS at each dose level) in the subjects taking oral steroids than in those not receiving concomitant medication. The AUC values of desmethylselegiline increased in a dose linear manner in subjects with no concomitant medication, but not in the oral steroid group. The metabolic ratio (AUC(desmethylselegiline)/AUC(selegiline)) was several-fold lower in the group receiving oral steroids compared with the no-concomitant-medication group (P<0.005 at all the four dose levels). CONCLUSIONS: Concomitant use of oral contraceptives caused a drastic (20-fold) increase in the oral bioavailability of selegiline. The highly significant difference in the metabolic ratio between the groups provides evidence that the mechanism of the interaction between selegiline and female sex steroids involves reduced T-demethylation of selegiline. The present results suggest that concomitant use of selegiline with exogenous female sex steroids should be avoided or the dosage of selegiline should be reduced in order to minimize the risks of selegiline related adverse drug reactions.  (+info)

Amphetamines induce apoptosis and regulation of bcl-x splice variants in neocortical neurons. (4/566)

Amphetamineanalogs have emerged as popular recreational drugs of abuse. The number of reports of these substances producing severe acute toxicity and death is increasing. In 'Ecstasy' -associated deaths, focal necrosis in the liver and individual myocytic necrosis has been reported. Furthermore, serotonergic and dopaminergic neuronal cell damage has been observed in experimental amphetamine intoxication in laboratory animals. Here we demonstrate that subchronic exposure to D-amphetamine, methamphetamine, methylenedioxyamphetamine, and methylenedioxymethamphetamine ('Ecstasy') results in significant neurotoxicity in rat neocortical neurons in vitro. This neuronal cell death is accompanied by endonucleosomal DNA cleavage and differential expression of anti- and proapoptotic bcl-xL/S splice variants. In addition, we observed pronounced induction of cell stress-associated transcription factor c-jun and translation initiation inhibitor p97 after amphetamine treatment. These data support that the neurotoxic effects of different amphetamines are extended to rat neocortical neurons and that apoptotic pathways are involved in amphetamine-induced neurotoxicity.  (+info)

Amphetamine and fenproporex levels following multidose administration of fenproporex. (5/566)

Drugs that are metabolized to amphetamine or methamphetamine are potentially of significant concern in the interpretation of positive drug-testing results for amphetamines. A number of different drugs have been reported to produce amphetamine in the urine of users. One of these compounds, fenproporex, has been shown to be metabolized to amphetamine, and previous reports indicated the parent compound could be detected at low levels for up to 48 h. Administration of fenproporex for seven days (one 10-mg dose per day) to five healthy volunteers resulted in amphetamine being detected in the urine of all subjects. Peak concentrations of amphetamine ranged from approximately 2850 to 4150 ng/mL. Amphetamine could be detected (> or = 5 ng/mL) in the urine for up to nearly 170 h after the last dose. Analysis of the metabolically produced amphetamine showed the presence of both enantiomers, which can be helpful in the differentiation of some illicit amphetamine use from the use of this precursor drug. In addition, evaluation of the enantiomeric composition of the metabolite (amphetamine) can be a valuable tool in the interpretation of time since last dose. More significantly, all samples that contained amphetamine at a concentration of > or = 500 ng/mL were shown to also contain detectable amounts of the parent compound.  (+info)

The evolution of cerebral blood flow in the developing brain: evaluation with iodine-123 iodoamphetamine SPECT and correlation with MR imaging. (6/566)

BACKGROUND AND PURPOSE: Although it is well established that brain maturation correlates temporally with the functions the newborn or infant performs at various stages of development, the precise relationship between function and anatomic brain maturation remains unclear. The purpose of this study was to investigate the developmental changes of regional cerebral blood flow (rCBF) in infants and children using iodine-123 iodoamphetamine (123I-IMP) and single-photon emission computed tomography (SPECT). These findings were correlated with the MR imaging appearance of the brain and with known developmental changes. METHODS: Twenty-one 123I-IMP SPECT examinations of 17 patients, ranging in age from neonates to 2 years, were reviewed retrospectively. All children had had transient neurologic events in the neonatal period that did not significantly affect subsequent neuropsychological development. MR studies were performed in 12 of these patients and the MR findings were correlated with the SPECT results. RESULTS: SPECT studies showed a consistent pattern of evolving changes in 123I-IMP uptake, most likely reflecting evolution of rCBF. From the 34th postconceptional week until the end of the second month after term delivery, there was predominant uptake in the thalami, brain stem, and paleocerebellum, with relatively less cortical activity. Radionuclide uptake in both the perirolandic and occipital cortices was well seen around the 40th postconceptional week and increased rapidly thereafter, with a predominance of parietal activity. By 3 months, radionuclide uptake in the cerebellar hemispheres and parietofrontal cortices increased. Frontal and temporal activity increased by age 6 to 8 months. Uptake in the basal ganglia increased by 8 months. By the beginning of the second year, rCBF showed a similar topographic pattern to that in adults. CONCLUSION: The time course of the changes in 123I-IMP uptake in the developing brain as detected by SPECT is similar to that of myelination and most likely reflects an overall topologic maturational pattern of the brain.  (+info)

Direct agonists for serotonin receptors enhance locomotor function in rats that received neural transplants after neonatal spinal transection. (7/566)

We analyzed whether acute treatment with serotonergic agonists would improve motor function in rats with transected spinal cords (spinal rats) and in rats that received transplants of fetal spinal cord into the transection site (transplant rats). Neonates received midthoracic spinal transections within 48 hr of birth; transplant rats received fetal (embryonic day 14) spinal cord grafts at the time of transection. At 3 weeks, rats began 1-2 months of training in treadmill locomotion. Rats in the transplant group developed better weight-supported stepping than spinal rats. Systemic administration of two directly acting agonists for serotonergic 5-HT(2) receptor subtypes, quipazine and (+/-)-1-[2, 5]-dimethoxy-4-iodophenyl-2-aminopropane), further increased weight-supported stepping in transplant rats. The improvement was dose-dependent and greatest in rats with poor to moderate baseline weight support. In contrast, indirectly acting serotonergic agonists, which block reuptake of 5-HT (sertraline) or release 5-HT and block its reuptake (D-fenfluramine), failed to enhance motor function. Neither direct nor indirect agonists significantly improved locomotion in spinal rats as a group, despite equivalent upregulation of 5-HT(2) receptors in the lumbar ventral horn of lesioned rats with and without transplants. The distribution of immunoreactive serotonergic fibers within and caudal to the transplant did not appear to correspond to restoration of motor function. Our results confirm our previous demonstration that transplants improve motor performance in spinal rats. Additional stimulation with agonists at subtypes of 5-HT receptors produces a beneficial interaction with transplants that further improves motor competence.  (+info)

Evidence for a role for central 5-HT2B as well as 5-HT2A receptors in cardiovascular regulation in anaesthetized rats. (8/566)

1. The effects of injections i.c.v. of quipazine, (2 micromol kg-1) and 1-(2,5-di-methoxy-4-iodophenyl)-2-aminopropane (DOI; 2 micromol kg-1) on renal sympathetic and phrenic nerve activity, mean arterial blood pressure (MAP) and heart rate were investigated in alpha-chloralose anaesthetized rats pretreated with a peripherally acting 5-HT2 receptor antagonist. 2. Quipazine or DOI caused a rise in MAP which was associated with a tachycardia and renal sympathoinhibition in rats pretreated (i.c.v.) with the antagonist vehicle 10% PEG. These effects of quipazine were completely blocked by pretreatment with cinanserin (a 5-HT2 receptor antagonist) and attenuated by spiperone (a 5-HT2A receptor antagonist). However, pretreatment with SB200646A (a 5-HT2B/2C receptor antagonist) only blocked the sympathoinhibition, while pretreatment with SB204741 (a 5-HT2B receptor antagonist) reversed the sympathoinhibition to excitation as it also did for DOI. Quipazine also caused renal sympathoexcitation in the presence (i.v.) of a vasopressin V1 receptor antagonist. 3. Injection (i.v.) of the V1 receptor antagonist at the peak pressor response evoked by quipazine alone and in the presence of SB204741 caused an immediate fall in MAP. For quipazine alone the renal sympathoinhibition was slowly reversed to an excitation, while the renal sympathoexcitation observed in the presence of SB204741 was potentiated. In both, the quipazine-evoked tachycardia was unaffected. 4. The data indicate that cardiovascular responses caused by i.c.v. quipazine and DOI are primarily due to activation of central 5-HT2A receptors, which causes the release of vasopressin and a tachycardia. This released vasopressin appears to suppress a 5-HT2A receptor-evoked central increase in sympathetic outflow, which involves the activation of central 5-HT2B receptors indirectly by the released vasopressin.  (+info)

Amphetamine is a central nervous system stimulant drug that works by increasing the levels of certain neurotransmitters (chemical messengers) in the brain, such as dopamine and norepinephrine. It is used medically to treat conditions such as attention deficit hyperactivity disorder (ADHD), narcolepsy, and obesity, due to its appetite-suppressing effects.

Amphetamines can be prescribed in various forms, including tablets, capsules, or liquids, and are available under several brand names, such as Adderall, Dexedrine, and Vyvanse. They are also known by their street names, such as speed, uppers, or wake-ups, and can be abused for their euphoric effects and ability to increase alertness, energy, and concentration.

Long-term use of amphetamines can lead to dependence, tolerance, and addiction, as well as serious health consequences, such as cardiovascular problems, mental health disorders, and malnutrition. It is essential to use amphetamines only under the supervision of a healthcare provider and follow their instructions carefully.

Amphetamines are a type of central nervous system stimulant drug that increases alertness, wakefulness, and energy levels. They work by increasing the activity of certain neurotransmitters (chemical messengers) in the brain, such as dopamine and norepinephrine. Amphetamines can be prescribed for medical conditions such as attention deficit hyperactivity disorder (ADHD) and narcolepsy, but they are also commonly abused for their ability to produce euphoria, increase confidence, and improve performance in tasks that require sustained attention.

Some common examples of amphetamines include:

* Adderall: a combination of amphetamine and dextroamphetamine, used to treat ADHD and narcolepsy
* Dexedrine: a brand name for dextroamphetamine, used to treat ADHD and narcolepsy
* Vyvanse: a long-acting formulation of lisdexamfetamine, a prodrug that is converted to dextroamphetamine in the body, used to treat ADHD

Amphetamines can be taken orally, snorted, smoked, or injected. Long-term use or abuse of amphetamines can lead to a number of negative health consequences, including addiction, cardiovascular problems, malnutrition, mental health disorders, and memory loss.

Central nervous system (CNS) stimulants are a class of drugs that increase alertness, attention, energy, and/or mood by directly acting on the brain. They can be prescribed to treat medical conditions such as narcolepsy, attention deficit hyperactivity disorder (ADHD), and depression that has not responded to other treatments.

Examples of CNS stimulants include amphetamine (Adderall), methylphenidate (Ritalin, Concerta), and modafinil (Provigil). These medications work by increasing the levels of certain neurotransmitters, such as dopamine and norepinephrine, in the brain.

In addition to their therapeutic uses, CNS stimulants are also sometimes misused for non-medical reasons, such as to enhance cognitive performance or to get high. However, it's important to note that misusing these drugs can lead to serious health consequences, including addiction, cardiovascular problems, and mental health issues.

Dextroamphetamine is a central nervous system stimulant that is used in the treatment of attention deficit hyperactivity disorder (ADHD) and narcolepsy. It works by increasing the levels of certain neurotransmitters, such as dopamine and norepinephrine, in the brain. Dextroamphetamine is available as a prescription medication and is sold under various brand names, including Adderall and Dexedrine. It is important to use this medication only as directed by a healthcare professional, as it can have potentially serious side effects if used improperly.

Amphetamine-related disorders are a category of mental disorders related to the use of amphetamines or similar stimulant drugs. According to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), there are several specific amphetamine-related disorders:

1. Amphetamine Use Disorder: This disorder is characterized by a problematic pattern of amphetamine use leading to clinically significant impairment or distress. The symptoms include increased tolerance, withdrawal, unsuccessful attempts to cut down or quit using, and continued use despite negative consequences.
2. Amphetamine Intoxication: This disorder occurs when an individual uses amphetamines and experiences symptoms such as agitation, aggression, hallucinations, delusions, tachycardia, hypertension, and elevated body temperature.
3. Amphetamine Withdrawal: This disorder is characterized by a cluster of symptoms that occur after cessation or reduction in amphetamine use, including dysphoric mood, fatigue, increased appetite, sleep disturbances, vivid dreams, and slowing of psychomotor activity.
4. Other Specified Amphetamine-Related Disorder: This category is used when an individual experiences significant problems related to amphetamine use that do not meet the full criteria for any of the other disorders in this category.
5. Unspecified Amphetamine-Related Disorder: This category is used when an individual experiences significant problems related to amphetamine use, but the specific diagnosis cannot be determined due to insufficient information or because the clinician chooses not to specify the reason.

It's important to note that amphetamines are a class of drugs that include prescription stimulants such as Adderall and Ritalin, as well as illicit substances like methamphetamine. Amphetamine-related disorders can have serious consequences for an individual's physical and mental health, relationships, and overall quality of life.

Methamphetamine is a powerful, highly addictive central nervous system stimulant that affects brain chemistry, leading to mental and physical dependence. Its chemical formula is N-methylamphetamine, and it is structurally similar to amphetamine but has additional methyl group, which makes it more potent and longer-lasting.

Methamphetamine exists in various forms, including crystalline powder (commonly called "meth" or "crystal meth") and a rocklike form called "glass." It can be taken orally, snorted, smoked, or injected after being dissolved in water or alcohol.

Methamphetamine use leads to increased levels of dopamine, a neurotransmitter responsible for reward, motivation, and reinforcement, resulting in euphoria, alertness, and energy. Prolonged use can cause severe psychological and physiological harm, including addiction, psychosis, cardiovascular issues, dental problems (meth mouth), and cognitive impairments.

Substance abuse detection refers to the process of identifying the use or misuse of psychoactive substances, such as alcohol, illicit drugs, or prescription medications, in an individual. This can be done through various methods, including:

1. Physical examination: A healthcare professional may look for signs of substance abuse, such as track marks, enlarged pupils, or unusual behavior.
2. Laboratory tests: Urine, blood, hair, or saliva samples can be analyzed to detect the presence of drugs or their metabolites. These tests can provide information about recent use (hours to days) or longer-term use (up to several months).
3. Self-report measures: Individuals may be asked to complete questionnaires or interviews about their substance use patterns and behaviors.
4. Observational assessments: In some cases, such as in a treatment setting, healthcare professionals may observe an individual's behavior over time to identify patterns of substance abuse.

Substance abuse detection is often used in clinical, workplace, or legal settings to assess individuals for potential substance use disorders, monitor treatment progress, or ensure compliance with laws or regulations.

N-Methyl-3,4-methylenedioxyamphetamine (also known as MDA) is a synthetic psychoactive drug that belongs to the class of amphetamines. It acts as a central nervous system stimulant and hallucinogen. Chemically, it is a derivative of amphetamine with an additional methylenedioxy ring attached to the 3,4 positions on the aromatic ring. MDA is known for its empathogenic effects, meaning that it can produce feelings of empathy, emotional openness, and euphoria in users. It has been used recreationally as a party drug and at raves, but it also has potential therapeutic uses. However, MDA can have serious side effects, including increased heart rate and blood pressure, hyperthermia, dehydration, and in some cases, serotonin syndrome. As with other psychoactive drugs, MDA should only be used under medical supervision and with a clear understanding of its potential risks and benefits.

Dopamine is a type of neurotransmitter, which is a chemical messenger that transmits signals in the brain and nervous system. It plays several important roles in the body, including:

* Regulation of movement and coordination
* Modulation of mood and motivation
* Control of the reward and pleasure centers of the brain
* Regulation of muscle tone
* Involvement in memory and attention

Dopamine is produced in several areas of the brain, including the substantia nigra and the ventral tegmental area. It is released by neurons (nerve cells) and binds to specific receptors on other neurons, where it can either excite or inhibit their activity.

Abnormalities in dopamine signaling have been implicated in several neurological and psychiatric conditions, including Parkinson's disease, schizophrenia, and addiction.

Stereotyped behavior, in the context of medicine and psychology, refers to repetitive, rigid, and invariant patterns of behavior or movements that are purposeless and often non-functional. These behaviors are not goal-directed or spontaneous and typically do not change in response to environmental changes or social interactions.

Stereotypies can include a wide range of motor behaviors such as hand flapping, rocking, head banging, body spinning, self-biting, or complex sequences of movements. They are often seen in individuals with developmental disabilities, intellectual disabilities, autism spectrum disorder, and some mental health conditions.

Stereotyped behaviors can also be a result of substance abuse, neurological disorders, or brain injuries. In some cases, these behaviors may serve as a self-soothing mechanism or a way to cope with stress, anxiety, or boredom. However, they can also interfere with daily functioning and social interactions, and in severe cases, may cause physical harm to the individual.

3,4-Methylenedioxyamphetamine (MDA) is a psychoactive drug that belongs to the amphetamine class. It is also known as "ecstasy" or "molly." MDA acts as a stimulant, hallucinogen, and entactogen, which means it can produce feelings of increased energy, emotional warmth, and empathy.

MDA is illegal in many countries, including the United States, due to its potential for abuse and the risk of serious adverse effects. Some of the negative consequences associated with MDA use include nausea, vomiting, muscle tension, teeth grinding, increased heart rate and blood pressure, and hyperthermia (elevated body temperature). In high doses or when used in combination with other substances, MDA can cause seizures, coma, and even death.

It is important to note that the use of illegal drugs like MDA carries significant legal and health risks. If you are concerned about your own or someone else's drug use, it is recommended that you seek help from a qualified healthcare professional.

The nucleus accumbens is a part of the brain that is located in the ventral striatum, which is a key region of the reward circuitry. It is made up of two subregions: the shell and the core. The nucleus accumbens receives inputs from various sources, including the prefrontal cortex, amygdala, and hippocampus, and sends outputs to the ventral pallidum and other areas.

The nucleus accumbens is involved in reward processing, motivation, reinforcement learning, and addiction. It plays a crucial role in the release of the neurotransmitter dopamine, which is associated with pleasure and reinforcement. Dysfunction in the nucleus accumbens has been implicated in various neurological and psychiatric conditions, including substance use disorders, depression, and obsessive-compulsive disorder.

Dopamine agents are medications that act on dopamine receptors in the brain. Dopamine is a neurotransmitter, a chemical messenger that transmits signals in the brain and other areas of the body. It plays important roles in many functions, including movement, motivation, emotion, and cognition.

Dopamine agents can be classified into several categories based on their mechanism of action:

1. Dopamine agonists: These medications bind to dopamine receptors and mimic the effects of dopamine. They are used to treat conditions such as Parkinson's disease, restless legs syndrome, and certain types of dopamine-responsive dystonia. Examples include pramipexole, ropinirole, and rotigotine.
2. Dopamine precursors: These medications provide the building blocks for the body to produce dopamine. Levodopa is a commonly used dopamine precursor that is converted to dopamine in the brain. It is often used in combination with carbidopa, which helps to prevent levodopa from being broken down before it reaches the brain.
3. Dopamine antagonists: These medications block the action of dopamine at its receptors. They are used to treat conditions such as schizophrenia and certain types of nausea and vomiting. Examples include haloperidol, risperidone, and metoclopramide.
4. Dopamine reuptake inhibitors: These medications increase the amount of dopamine available in the synapse (the space between two neurons) by preventing its reuptake into the presynaptic neuron. They are used to treat conditions such as attention deficit hyperactivity disorder (ADHD) and depression. Examples include bupropion and nomifensine.
5. Dopamine release inhibitors: These medications prevent the release of dopamine from presynaptic neurons. They are used to treat conditions such as Tourette's syndrome and certain types of chronic pain. Examples include tetrabenazine and deutetrabenazine.

It is important to note that dopamine agents can have significant side effects, including addiction, movement disorders, and psychiatric symptoms. Therefore, they should be used under the close supervision of a healthcare provider.

"Motor activity" is a general term used in the field of medicine and neuroscience to refer to any kind of physical movement or action that is generated by the body's motor system. The motor system includes the brain, spinal cord, nerves, and muscles that work together to produce movements such as walking, talking, reaching for an object, or even subtle actions like moving your eyes.

Motor activity can be voluntary, meaning it is initiated intentionally by the individual, or involuntary, meaning it is triggered automatically by the nervous system without conscious control. Examples of voluntary motor activity include deliberately lifting your arm or kicking a ball, while examples of involuntary motor activity include heartbeat, digestion, and reflex actions like jerking your hand away from a hot stove.

Abnormalities in motor activity can be a sign of neurological or muscular disorders, such as Parkinson's disease, cerebral palsy, or multiple sclerosis. Assessment of motor activity is often used in the diagnosis and treatment of these conditions.

'Animal behavior' refers to the actions or responses of animals to various stimuli, including their interactions with the environment and other individuals. It is the study of the actions of animals, whether they are instinctual, learned, or a combination of both. Animal behavior includes communication, mating, foraging, predator avoidance, and social organization, among other things. The scientific study of animal behavior is called ethology. This field seeks to understand the evolutionary basis for behaviors as well as their physiological and psychological mechanisms.

Gas Chromatography-Mass Spectrometry (GC-MS) is a powerful analytical technique that combines the separating power of gas chromatography with the identification capabilities of mass spectrometry. This method is used to separate, identify, and quantify different components in complex mixtures.

In GC-MS, the mixture is first vaporized and carried through a long, narrow column by an inert gas (carrier gas). The various components in the mixture interact differently with the stationary phase inside the column, leading to their separation based on their partition coefficients between the mobile and stationary phases. As each component elutes from the column, it is then introduced into the mass spectrometer for analysis.

The mass spectrometer ionizes the sample, breaks it down into smaller fragments, and measures the mass-to-charge ratio of these fragments. This information is used to generate a mass spectrum, which serves as a unique "fingerprint" for each compound. By comparing the generated mass spectra with reference libraries or known standards, analysts can identify and quantify the components present in the original mixture.

GC-MS has wide applications in various fields such as forensics, environmental analysis, drug testing, and research laboratories due to its high sensitivity, specificity, and ability to analyze volatile and semi-volatile compounds.

Dopamine uptake inhibitors are a class of medications that work by blocking the reuptake of dopamine, a neurotransmitter, into the presynaptic neuron. This results in an increased concentration of dopamine in the synapse, leading to enhanced dopaminergic transmission and activity.

These drugs are used in various medical conditions where dopamine is implicated, such as depression, attention deficit hyperactivity disorder (ADHD), and neurological disorders like Parkinson's disease. They can also be used to treat substance abuse disorders, such as cocaine addiction, by blocking the reuptake of dopamine and reducing the rewarding effects of the drug.

Examples of dopamine uptake inhibitors include:

* Bupropion (Wellbutrin), which is used to treat depression and ADHD
* Methylphenidate (Ritalin, Concerta), which is used to treat ADHD
* Amantadine (Symmetrel), which is used to treat Parkinson's disease and also has antiviral properties.

It's important to note that dopamine uptake inhibitors can have side effects, including increased heart rate, blood pressure, and anxiety. They may also have the potential for abuse and dependence, particularly in individuals with a history of substance abuse. Therefore, these medications should be used under the close supervision of a healthcare provider.

"Street drugs" is a colloquial term rather than medical jargon, but it generally refers to illegal substances or medications that are used without a prescription. These can include a wide variety of drugs such as marijuana, cocaine, heroin, methamphetamines, ecstasy, LSD, and many others. They are called "street drugs" because they are often bought and sold on the street or in clandestine settings, rather than through legitimate pharmacies or medical professionals. It's important to note that these substances can be highly dangerous and addictive, with serious short-term and long-term health consequences.

Designer drugs are synthetic or chemically altered substances that are designed to mimic the effects of controlled substances. They are often created in clandestine laboratories and marketed as legal alternatives to illegal drugs. These drugs are called "designer" because they are intentionally modified to avoid detection and regulation by law enforcement agencies and regulatory bodies.

Designer drugs can be extremely dangerous, as their chemical composition is often unknown or only partially understood. They may contain potentially harmful impurities or variations that can lead to unpredictable and sometimes severe health consequences. Examples of designer drugs include synthetic cannabinoids (such as "Spice" or "K2"), synthetic cathinones (such as "bath salts"), and novel psychoactive substances (NPS).

It is important to note that while some designer drugs may be legal at the time they are manufactured and sold, their possession and use may still be illegal under federal or state laws. Additionally, many designer drugs have been made illegal through scheduling by the Drug Enforcement Administration (DEA) or through legislation specifically targeting them.

Appetite depressants are medications or substances that reduce or suppress feelings of hunger and appetite. They can be prescribed to treat various medical conditions, such as obesity or binge eating disorder, where weight loss is a recommended treatment goal. Some common appetite depressants include:

1. Phentermine: This medication works by stimulating the release of certain neurotransmitters in the brain that help suppress appetite and increase metabolism. It is often prescribed for short-term use (up to 12 weeks) as part of a comprehensive weight loss plan.

2. Diethylpropion: Similar to phentermine, diethylpropion stimulates the release of neurotransmitters that suppress appetite and increase metabolism. It is also prescribed for short-term use in treating obesity.

3. Naltrexone-bupropion (Contrave): This combination medication helps manage weight by reducing appetite and increasing feelings of fullness. Naltrexone is an opioid antagonist that blocks the rewarding effects of food, while bupropion is an antidepressant that can help reduce cravings for high-calorie foods.

4. Lorcaserin (Belviq): This medication works by selectively activating serotonin receptors in the brain, which helps promote satiety and reduce appetite. It was withdrawn from the US market in 2020 due to concerns about its potential link to an increased risk of cancer.

5. Topiramate (Topamax): Although primarily used as an anticonvulsant, topiramate has also been found to have appetite-suppressing effects. It is often combined with phentermine in a single formulation (Qsymia) for the treatment of obesity.

6. Cannabis: Some studies suggest that cannabinoids, the active compounds in marijuana, may help reduce hunger and promote weight loss by interacting with the endocannabinoid system in the body. However, more research is needed to fully understand its potential as an appetite depressant.

It's important to note that appetite suppressants should only be used under the guidance of a healthcare professional and as part of a comprehensive weight management plan. These medications can have side effects and potential risks, so it's crucial to discuss their use with your doctor before starting any new treatment regimen.

Cocaine is a highly addictive stimulant drug derived from the leaves of the coca plant (Erythroxylon coca). It is a powerful central nervous system stimulant that affects the brain and body in many ways. When used recreationally, cocaine can produce feelings of euphoria, increased energy, and mental alertness; however, it can also cause serious negative consequences, including addiction, cardiovascular problems, seizures, and death.

Cocaine works by increasing the levels of dopamine in the brain, a neurotransmitter associated with pleasure and reward. This leads to the pleasurable effects that users seek when they take the drug. However, cocaine also interferes with the normal functioning of the brain's reward system, making it difficult for users to experience pleasure from natural rewards like food or social interactions.

Cocaine can be taken in several forms, including powdered form (which is usually snorted), freebase (a purer form that is often smoked), and crack cocaine (a solid form that is typically heated and smoked). Each form of cocaine has different risks and potential harms associated with its use.

Long-term use of cocaine can lead to a number of negative health consequences, including addiction, heart problems, malnutrition, respiratory issues, and mental health disorders like depression or anxiety. It is important to seek help if you or someone you know is struggling with cocaine use or addiction.

Dopamine plasma membrane transport proteins, also known as dopamine transporters (DAT), are a type of protein found in the cell membrane that play a crucial role in the regulation of dopamine neurotransmission. They are responsible for the reuptake of dopamine from the synaptic cleft back into the presynaptic neuron, thereby terminating the signal transduction of dopamine and regulating the amount of dopamine available for further release.

Dopamine transporters belong to the family of sodium-dependent neurotransmitter transporters and are encoded by the SLC6A3 gene in humans. Abnormalities in dopamine transporter function have been implicated in several neurological and psychiatric disorders, including Parkinson's disease, attention deficit hyperactivity disorder (ADHD), and substance use disorders.

In summary, dopamine plasma membrane transport proteins are essential for the regulation of dopamine neurotransmission by mediating the reuptake of dopamine from the synaptic cleft back into the presynaptic neuron.

Sprague-Dawley rats are a strain of albino laboratory rats that are widely used in scientific research. They were first developed by researchers H.H. Sprague and R.C. Dawley in the early 20th century, and have since become one of the most commonly used rat strains in biomedical research due to their relatively large size, ease of handling, and consistent genetic background.

Sprague-Dawley rats are outbred, which means that they are genetically diverse and do not suffer from the same limitations as inbred strains, which can have reduced fertility and increased susceptibility to certain diseases. They are also characterized by their docile nature and low levels of aggression, making them easier to handle and study than some other rat strains.

These rats are used in a wide variety of research areas, including toxicology, pharmacology, nutrition, cancer, and behavioral studies. Because they are genetically diverse, Sprague-Dawley rats can be used to model a range of human diseases and conditions, making them an important tool in the development of new drugs and therapies.

The corpus striatum is a part of the brain that plays a crucial role in movement, learning, and cognition. It consists of two structures called the caudate nucleus and the putamen, which are surrounded by the external and internal segments of the globus pallidus. Together, these structures form the basal ganglia, a group of interconnected neurons that help regulate voluntary movement.

The corpus striatum receives input from various parts of the brain, including the cerebral cortex, thalamus, and other brainstem nuclei. It processes this information and sends output to the globus pallidus and substantia nigra, which then project to the thalamus and back to the cerebral cortex. This feedback loop helps coordinate and fine-tune movements, allowing for smooth and coordinated actions.

Damage to the corpus striatum can result in movement disorders such as Parkinson's disease, Huntington's disease, and dystonia. These conditions are characterized by abnormal involuntary movements, muscle stiffness, and difficulty initiating or controlling voluntary movements.

Hallucinogens are a class of psychoactive substances that alter perception, mood, and thought, often causing hallucinations, which are profound distortions in a person's perceptions of reality. These substances work by disrupting the normal functioning of the brain, particularly the parts that regulate mood, sensory perception, sleep, hunger, and sexual behavior.

Hallucinogens can be found in various forms, including plants, mushrooms, and synthetic compounds. Some common examples of hallucinogens include LSD (d-lysergic acid diethylamide), psilocybin (found in certain species of mushrooms), DMT (dimethyltryptamine), and ayahuasca (a plant-based brew from South America).

The effects of hallucinogens can vary widely depending on the specific substance, the dose, the individual's personality, mood, and expectations, and the environment in which the drug is taken. These effects can range from pleasant sensory experiences and heightened emotional awareness to terrifying hallucinations and overwhelming feelings of anxiety or despair.

It's important to note that hallucinogens can be dangerous, particularly when taken in high doses or in combination with other substances. They can also cause long-term psychological distress and may trigger underlying mental health conditions. As such, they should only be used under the guidance of a trained medical professional for therapeutic purposes.

The Enzyme Multiplied Immunoassay Technique (EMIT) is a type of immunoassay used for the quantitative or qualitative determination of various substances, such as drugs, hormones, or antibodies. The technique utilizes an enzyme-linked antigen or antibody that reacts with the substance being measured (analyte) in the sample to form an immune complex. This complex then interacts with a second enzyme-labeled antigen or antibody, leading to the formation of an enzyme-analyte-enzyme "sandwich." The enzymes present in this sandwich are capable of catalyzing a reaction that produces a colored product, which can be measured spectrophotometrically.

The amount of color produced is proportional to the concentration of the analyte present in the sample. This allows for the determination of the analyte's concentration through comparison with a standard curve generated using samples with known concentrations of the analyte. EMIT is widely used in clinical laboratories for diagnostic and therapeutic drug monitoring purposes, as well as in forensic toxicology to detect drugs of abuse.

In summary, Enzyme Multiplied Immunoassay Technique (EMIT) is a sensitive and specific immunoassay method that utilizes enzyme-labeled antigens or antibodies to quantitatively or qualitatively measure the concentration of various substances in a sample.

Forensic medicine, also known as legal medicine or medical jurisprudence, is a branch of medicine that deals with the application of medical knowledge to legal issues and questions. It involves the examination, interpretation, and analysis of medical evidence for use in courts of law. This may include determining the cause and manner of death, identifying injuries or diseases, assessing the effects of substances or treatments, and evaluating the competency or capacity of individuals. Forensic medicine is often used in criminal investigations and court cases, but it can also be applied to civil matters such as personal injury claims or medical malpractice suits.

Methylphenidate is a central nervous system (CNS) stimulant drug that is primarily used in the treatment of attention deficit hyperactivity disorder (ADHD) and narcolepsy. It works by increasing the levels of neurotransmitters, such as dopamine and norepinephrine, in the brain, which helps to improve focus, concentration, and alertness.

Methylphenidate is available under various brand names, including Ritalin, Concerta, and Methylin, among others. It comes in different forms, such as tablets, capsules, or extended-release formulations, and is typically taken orally. The dosage and duration of treatment are usually individualized based on the patient's response to the medication and any potential side effects.

It is important to note that methylphenidate has a high potential for abuse and addiction, and its use should be closely monitored by a healthcare professional. Additionally, it can interact with other medications and medical conditions, so it is essential to inform your doctor of any health concerns before starting treatment with methylphenidate.

A dose-response relationship in the context of drugs refers to the changes in the effects or symptoms that occur as the dose of a drug is increased or decreased. Generally, as the dose of a drug is increased, the severity or intensity of its effects also increases. Conversely, as the dose is decreased, the effects of the drug become less severe or may disappear altogether.

The dose-response relationship is an important concept in pharmacology and toxicology because it helps to establish the safe and effective dosage range for a drug. By understanding how changes in the dose of a drug affect its therapeutic and adverse effects, healthcare providers can optimize treatment plans for their patients while minimizing the risk of harm.

The dose-response relationship is typically depicted as a curve that shows the relationship between the dose of a drug and its effect. The shape of the curve may vary depending on the drug and the specific effect being measured. Some drugs may have a steep dose-response curve, meaning that small changes in the dose can result in large differences in the effect. Other drugs may have a more gradual dose-response curve, where larger changes in the dose are needed to produce significant effects.

In addition to helping establish safe and effective dosages, the dose-response relationship is also used to evaluate the potential therapeutic benefits and risks of new drugs during clinical trials. By systematically testing different doses of a drug in controlled studies, researchers can identify the optimal dosage range for the drug and assess its safety and efficacy.

P-Chloroamphetamine, also known as PCA or 4-chloroamphetamine, is a synthetic stimulant drug that has been used in scientific research but is not commonly used medically. It is a derivative of amphetamine and has similar effects, such as increasing heart rate, blood pressure, and alertness. However, it also has hallucinogenic properties and can cause psychological disturbances.

PCA acts as a releasing agent for the neurotransmitters dopamine, norepinephrine, and serotonin, which are involved in regulating mood, appetite, and other physiological processes. It is classified as a Schedule I controlled substance in the United States due to its high potential for abuse and lack of accepted medical use.

It's important to note that PCA is not approved for any medical use in humans and should only be used in a controlled research setting with appropriate safety measures in place.

Adrenergic uptake inhibitors are a class of medications that work by blocking the reuptake of neurotransmitters, such as norepinephrine and dopamine, into the presynaptic neuron. This results in an increase in the amount of neurotransmitter available to bind to postsynaptic receptors, leading to an enhancement of adrenergic transmission.

These medications are used in the treatment of various medical conditions, including depression, attention deficit hyperactivity disorder (ADHD), and narcolepsy. Some examples of adrenergic uptake inhibitors include:

* Tricyclic antidepressants (TCAs): These medications, such as imipramine and amitriptyline, were developed in the 1950s and are used to treat depression, anxiety disorders, and chronic pain.
* Selective serotonin-norepinephrine reuptake inhibitors (SNRIs): These medications, such as venlafaxine and duloxetine, were developed in the 1990s and are used to treat depression, anxiety disorders, and chronic pain.
* Norepinephrine-dopamine reuptake inhibitors (NDRIs): These medications, such as bupropion, are used to treat depression and ADHD.

It's important to note that these medications can have side effects and should be used under the supervision of a healthcare provider.

Dopamine agonists are a class of medications that mimic the action of dopamine, a neurotransmitter in the brain that regulates movement, emotion, motivation, and reinforcement of rewarding behaviors. These medications bind to dopamine receptors in the brain and activate them, leading to an increase in dopaminergic activity.

Dopamine agonists are used primarily to treat Parkinson's disease, a neurological disorder characterized by motor symptoms such as tremors, rigidity, bradykinesia (slowness of movement), and postural instability. By increasing dopaminergic activity in the brain, dopamine agonists can help alleviate some of these symptoms.

Examples of dopamine agonists include:

1. Pramipexole (Mirapex)
2. Ropinirole (Requip)
3. Rotigotine (Neupro)
4. Apomorphine (Apokyn)

Dopamine agonists may also be used off-label to treat other conditions, such as restless legs syndrome or certain types of dopamine-responsive dystonia. However, these medications can have significant side effects, including nausea, dizziness, orthostatic hypotension, compulsive behaviors (such as gambling, shopping, or sexual addiction), and hallucinations. Therefore, they should be used with caution and under the close supervision of a healthcare provider.

I'm sorry for any confusion, but "Methyltyrosines" is not a widely recognized medical term or concept in the field of medicine or biochemistry. It seems that there might be some misunderstanding or typo in your question.

If you are referring to "3-Methoxytyrosine" or "3-MT," it is a metabolite of dopamine, which is formed in the body by the enzyme catechol-O-methyltransferase (COMT). 3-MT can be measured in various biological samples, such as urine or plasma, to evaluate the activity of COMT and assess the exposure to drugs that inhibit this enzyme.

If you meant something else by "Methyltyrosines," please provide more context or clarify your question so I can give a more accurate answer.

The neostriatum is a component of the basal ganglia, a group of subcortical nuclei in the brain that are involved in motor control, procedural learning, and other cognitive functions. It is composed primarily of two types of neurons: medium spiny neurons and aspiny interneurons. The neostriatum receives input from various regions of the cerebral cortex and projects to other parts of the basal ganglia, forming an important part of the cortico-basal ganglia-thalamo-cortical loop.

In medical terminology, the neostriatum is often used interchangeably with the term "striatum," although some sources reserve the term "neostriatum" for the caudate nucleus and putamen specifically, while using "striatum" to refer to the entire structure including the ventral striatum (also known as the nucleus accumbens).

Damage to the neostriatum has been implicated in various neurological conditions, such as Huntington's disease and Parkinson's disease.

Microdialysis is a minimally invasive technique used in clinical and research settings to continuously monitor the concentration of various chemicals, such as neurotransmitters, drugs, or metabolites, in biological fluids (e.g., extracellular fluid of tissues, blood, or cerebrospinal fluid). This method involves inserting a small, flexible catheter with a semipermeable membrane into the region of interest. A physiological solution is continuously perfused through the catheter, allowing molecules to diffuse across the membrane based on their concentration gradient. The dialysate that exits the catheter is then collected and analyzed for target compounds using various analytical techniques (e.g., high-performance liquid chromatography, mass spectrometry).

In summary, microdialysis is a valuable tool for monitoring real-time changes in chemical concentrations within biological systems, enabling better understanding of physiological processes or pharmacokinetic properties of drugs.

Phenmetrazine is a stimulant drug that was previously used for the treatment of obesity, but its use has been discontinued in many countries due to its addictive potential and adverse effects. It acts as a central nervous system stimulant, increasing heart rate, blood pressure, and alertness, and decreasing appetite.

The medical definition of Phenmetrazine is:

A psychostimulant drug that has been used in the treatment of obesity but has been discontinued in many countries due to its addictive potential and adverse effects. It is a phenylpropylamine derivative, structurally related to amphetamine and methamphetamine, and acts as a central nervous system stimulant, increasing heart rate, blood pressure, and alertness, and decreasing appetite. Phenmetrazine has sympathomimetic effects, releasing catecholamines from presynaptic nerve endings and blocking their reuptake, resulting in increased concentrations of these neurotransmitters in the synaptic cleft. It also inhibits monoamine oxidase, further increasing the concentration of catecholamines in the brain.

Phenmetrazine is classified as a Schedule II controlled substance in the United States due to its high potential for abuse and dependence. Its use is limited to research purposes only and requires a special license from the Drug Enforcement Administration (DEA).

Dopamine antagonists are a class of drugs that block the action of dopamine, a neurotransmitter in the brain associated with various functions including movement, motivation, and emotion. These drugs work by binding to dopamine receptors and preventing dopamine from attaching to them, which can help to reduce the symptoms of certain medical conditions such as schizophrenia, bipolar disorder, and gastroesophageal reflux disease (GERD).

There are several types of dopamine antagonists, including:

1. Typical antipsychotics: These drugs are primarily used to treat psychosis, including schizophrenia and delusional disorders. Examples include haloperidol, chlorpromazine, and fluphenazine.
2. Atypical antipsychotics: These drugs are also used to treat psychosis but have fewer side effects than typical antipsychotics. They may also be used to treat bipolar disorder and depression. Examples include risperidone, olanzapine, and quetiapine.
3. Antiemetics: These drugs are used to treat nausea and vomiting. Examples include metoclopramide and prochlorperazine.
4. Dopamine agonists: While not technically dopamine antagonists, these drugs work by stimulating dopamine receptors and can be used to treat conditions such as Parkinson's disease. However, they can also have the opposite effect and block dopamine receptors in high doses, making them functionally similar to dopamine antagonists.

Common side effects of dopamine antagonists include sedation, weight gain, and movement disorders such as tardive dyskinesia. It's important to use these drugs under the close supervision of a healthcare provider to monitor for side effects and adjust the dosage as needed.

Nomifensine is a medication that was previously used in the treatment of depression, but it is no longer available in many countries due to safety concerns. It is a non-tricyclic antidepressant that works by inhibiting the reuptake of dopamine and noradrenaline, which helps to increase the levels of these neurotransmitters in the brain and improve mood.

The medical definition of Nomifensine is:

"Nomifensine is a non-tricyclic antidepressant that is a potent inhibitor of dopamine and noradrenaline reuptake, with minimal effects on serotonin reuptake. It was used in the treatment of depression but has been withdrawn from the market due to safety concerns."

It's important to note that Nomifensine should only be taken under the supervision of a medical professional, and it is not available in many countries due to its potential for causing serious side effects such as liver toxicity and the risk of developing a rare but potentially fatal condition called hemolytic anemia.

Pyrazolones are a group of non-steroidal anti-inflammatory drugs (NSAIDs) that contain a pyrazole ring in their chemical structure. They have analgesic, antipyretic, and anti-inflammatory properties. Pyrazolones include drugs such as phenylbutazone, oxyphenbutazone, and aminopyrine. However, due to their potential for serious side effects, including agranulocytosis (a severe decrease in white blood cells), pyrazolones are rarely used in modern clinical practice.

Dopamine D2 receptor is a type of metabotropic G protein-coupled receptor that binds to the neurotransmitter dopamine. It is one of five subtypes of dopamine receptors (D1-D5) and is encoded by the gene DRD2. The activation of D2 receptors leads to a decrease in the activity of adenylyl cyclase, which results in reduced levels of cAMP and modulation of ion channels.

D2 receptors are widely distributed throughout the central nervous system (CNS) and play important roles in various physiological functions, including motor control, reward processing, emotion regulation, and cognition. They are also involved in several neurological and psychiatric disorders, such as Parkinson's disease, schizophrenia, drug addiction, and Tourette syndrome.

D2 receptors have two main subtypes: D2 short (D2S) and D2 long (D2L). The D2S subtype is primarily located in the presynaptic terminals and functions as an autoreceptor that regulates dopamine release, while the D2L subtype is mainly found in the postsynaptic neurons and modulates intracellular signaling pathways.

Antipsychotic drugs, which are used to treat schizophrenia and other psychiatric disorders, work by blocking D2 receptors. However, excessive blockade of these receptors can lead to side effects such as extrapyramidal symptoms (EPS), tardive dyskinesia, and hyperprolactinemia. Therefore, the development of drugs that selectively target specific subtypes of dopamine receptors is an active area of research in the field of neuropsychopharmacology.

Ephedrine is a medication that stimulates the nervous system and is used to treat low blood pressure, asthma, and nasal congestion. It works by narrowing the blood vessels and increasing heart rate, which can help to increase blood pressure and open up the airways in the lungs. Ephedrine may also be used as a bronchodilator to treat COPD (chronic obstructive pulmonary disease).

Ephedrine is available in various forms, including tablets, capsules, and solutions for injection. It is important to follow the instructions of a healthcare provider when taking ephedrine, as it can have side effects such as rapid heart rate, anxiety, headache, and dizziness. Ephedrine should not be used by people with certain medical conditions, such as heart disease, high blood pressure, or narrow-angle glaucoma, and it should not be taken during pregnancy or breastfeeding without consulting a healthcare provider.

In addition to its medical uses, ephedrine has been used as a performance-enhancing drug and is banned by many sports organizations. It can also be found in some over-the-counter cold and allergy medications, although these products are required to carry warnings about the potential for misuse and addiction.

Fenfluramine is a drug that was previously used for the short-term treatment of obesity. It works by suppressing appetite and increasing the feeling of fullness. Fenfluramine is an amphetamine derivative and stimulates the release of serotonin, a neurotransmitter in the brain that helps regulate mood, appetite, and sleep.

Fenfluramine was commonly prescribed in combination with phentermine, another appetite suppressant, under the brand name Fen-Phen. However, in 1997, the U.S. Food and Drug Administration (FDA) issued a public health warning about the potential risk of serious heart valve damage associated with the use of fenfluramine and withdrew its approval for the drug's use. Since then, fenfluramine has not been approved for medical use in many countries, including the United States.

Substance-induced psychosis is a type of psychosis that is caused by the use of drugs, alcohol, or other substances. The American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) defines substance/medication-induced psychotic disorder as follows:

A. Presence of one (or more) of the following symptoms:

1. Delusions.
2. Hallucinations.
3. Disorganized speech (e.g., frequent derailment or incoherence).

B. There is evidence from the history, physical examination, or laboratory findings that the disturbance is caused by the direct physiological effects of a substance (e.g., a drug of abuse, a medication) or a combination of substances.

C. The disturbance does not occur exclusively during the course of a delirium and is not better explained by a psychotic disorder that is not substance/medication-induced. The symptoms in Criterion A developed during or soon after substance intoxication or withdrawal, or after exposure to a medication.

D. The disturbance causes significant distress or impairment in social, occupational, or other important areas of functioning.

E. The disturbance is not better accounted for by another mental disorder (e.g., major depressive disorder, bipolar disorder).

It's important to note that the diagnosis of substance-induced psychosis requires a thorough medical and psychiatric evaluation to determine if the symptoms are caused by substance use or another underlying mental health condition.

Benzphetamine is a sympathomimetic amine, which is a type of drug that stimulates the sympathetic nervous system. It is a central nervous system stimulant and an appetite suppressant. Benzphetamine is used as a short-term supplement to diet and exercise in the treatment of obesity.

The medical definition of benzphetamine is:

A CNS stimulant and anorectic, structurally related to amphetamines, but pharmacologically related to the phenylethylamines. It has a longer duration of action than other amphetamines because it is absorbed more slowly and is excreted more slowly. Benzphetamine is used as an appetite suppressant in the treatment of obesity.

It's important to note that benzphetamine, like other weight-loss medications, should be used in conjunction with a reduced-calorie diet and exercise. It also has a risk for abuse and dependence, so it is usually prescribed for short-term use only.

Operant conditioning is a type of learning in which behavior is modified by its consequences, either reinforcing or punishing the behavior. It was first described by B.F. Skinner and involves an association between a response (behavior) and a consequence (either reward or punishment). There are two types of operant conditioning: positive reinforcement, in which a desirable consequence follows a desired behavior, increasing the likelihood that the behavior will occur again; and negative reinforcement, in which a undesirable consequence is removed following a desired behavior, also increasing the likelihood that the behavior will occur again.

For example, if a child cleans their room (response) and their parent gives them praise or a treat (positive reinforcement), the child is more likely to clean their room again in the future. If a child is buckling their seatbelt in the car (response) and the annoying buzzer stops (negative reinforcement), the child is more likely to buckle their seatbelt in the future.

It's important to note that operant conditioning is a form of learning, not motivation. The behavior is modified by its consequences, regardless of the individual's internal state or intentions.

Substance Withdrawal Syndrome is a medically recognized condition that occurs when an individual who has been using certain substances, such as alcohol, opioids, or benzodiazepines, suddenly stops or significantly reduces their use. The syndrome is characterized by a specific set of symptoms that can be physical, cognitive, and emotional in nature. These symptoms can vary widely depending on the substance that was being used, the length and intensity of the addiction, and individual factors such as genetics, age, and overall health.

The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), published by the American Psychiatric Association, provides the following diagnostic criteria for Substance Withdrawal Syndrome:

A. The development of objective evidence of withdrawal, referring to the specific physiological changes associated with the particular substance, or subjective evidence of withdrawal, characterized by the individual's report of symptoms that correspond to the typical withdrawal syndrome for the substance.

B. The symptoms cause clinically significant distress or impairment in social, occupational, or other important areas of functioning.

C. The symptoms are not better explained by co-occurring mental, medical, or other substance use disorders.

D. The withdrawal syndrome is not attributable to another medical condition and is not better accounted for by another mental disorder.

The DSM-5 also specifies that the diagnosis of Substance Withdrawal Syndrome should be substance-specific, meaning that it should specify the particular class of substances (e.g., alcohol, opioids, benzodiazepines) responsible for the withdrawal symptoms. This is important because different substances have distinct withdrawal syndromes and require different approaches to management and treatment.

In general, Substance Withdrawal Syndrome can be a challenging and potentially dangerous condition that requires professional medical supervision and support during the detoxification process. The specific symptoms and their severity will vary depending on the substance involved, but they may include:

* For alcohol: tremors, seizures, hallucinations, agitation, anxiety, nausea, vomiting, and insomnia.
* For opioids: muscle aches, restlessness, lacrimation (tearing), rhinorrhea (runny nose), yawning, perspiration, chills, mydriasis (dilated pupils), piloerection (goosebumps), nausea or vomiting, diarrhea, and abdominal cramps.
* For benzodiazepines: anxiety, irritability, insomnia, restlessness, confusion, hallucinations, seizures, and increased heart rate and blood pressure.

It is essential to consult with a healthcare professional if you or someone you know is experiencing symptoms of Substance Withdrawal Syndrome. They can provide appropriate medical care, support, and referrals for further treatment as needed.

In the context of medicine, particularly in behavioral neuroscience and psychology, "reward" is not typically used as a definitive medical term. However, it generally refers to a positive outcome or incentive that reinforces certain behaviors, making them more likely to be repeated in the future. This can involve various stimuli such as food, water, sexual activity, social interaction, or drug use, among others.

In the brain, rewards are associated with the activation of the reward system, primarily the mesolimbic dopamine pathway, which includes the ventral tegmental area (VTA) and the nucleus accumbens (NAcc). The release of dopamine in these areas is thought to reinforce and motivate behavior linked to rewards.

It's important to note that while "reward" has a specific meaning in this context, it is not a formal medical diagnosis or condition. Instead, it is a concept used to understand the neural and psychological mechanisms underlying motivation, learning, and addiction.

The caudate nucleus is a part of the brain located within the basal ganglia, a group of structures that are important for movement control and cognition. It has a distinctive C-shaped appearance and plays a role in various functions such as learning, memory, emotion, and motivation. The caudate nucleus receives inputs from several areas of the cerebral cortex and sends outputs to other basal ganglia structures, contributing to the regulation of motor behavior and higher cognitive processes.

Hyperkinesis is not considered a formal medical diagnosis. However, the term is often used informally to refer to a state of excessive or involuntary muscle movements. It is sometimes used as a synonym for hyperkinetic movement disorders, which are a group of neurological conditions characterized by an excess of involuntary movements. Examples of hyperkinetic movement disorders include chorea, dystonia, tics, myoclonus, and stereotypies.

It is important to note that the term "hyperkinesis" is not used in the current diagnostic classifications such as the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) or the International Classification of Diseases (ICD-10). Instead, specific movement disorders are diagnosed and classified based on their underlying causes and symptoms.

The Ventral Tegmental Area (VTA) is a collection of neurons located in the midbrain that is part of the dopamine system. It is specifically known as the A10 group and is the largest source of dopaminergic neurons in the brain. These neurons project to various regions, including the prefrontal cortex, amygdala, hippocampus, and nucleus accumbens, and are involved in reward, motivation, addiction, and various cognitive functions. The VTA also contains GABAergic and glutamatergic neurons that modulate dopamine release and have various other functions.

Substance-related disorders, as defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5), refer to a group of conditions caused by the use of substances such as alcohol, drugs, or medicines. These disorders are characterized by a problematic pattern of using a substance that leads to clinically significant impairment or distress. They can be divided into two main categories: substance use disorders and substance-induced disorders. Substance use disorders involve a pattern of compulsive use despite negative consequences, while substance-induced disorders include conditions such as intoxication, withdrawal, and substance/medication-induced mental disorders. The specific diagnosis depends on the type of substance involved, the patterns of use, and the presence or absence of physiological dependence.

Alpha-Methyltyrosine (α-MT) is a synthetic amino acid that acts as an inhibitor of the enzyme tyrosine hydroxylase. This enzyme is a rate-limiting step in the biosynthesis of catecholamines, including neurotransmitters such as dopamine and norepinephrine. By inhibiting tyrosine hydroxylase, α-MT reduces the synthesis of these catecholamines, which can lead to various effects on the nervous system.

In medical contexts, α-MT has been used in research settings to study the functions of catecholamines and their role in various physiological processes. It has also been investigated as a potential treatment for certain conditions, such as hypertension and anxiety disorders, although its clinical use is not widespread due to its side effects and limited efficacy.

It's important to note that α-MT should only be used under the supervision of a medical professional, as it can have significant effects on the nervous system and may interact with other medications or health conditions.

Serotonin agents are a class of drugs that work on the neurotransmitter serotonin (5-hydroxytryptamine, 5-HT) in the brain and elsewhere in the body. They include several types of medications such as:

1. Selective Serotonin Reuptake Inhibitors (SSRIs): These drugs block the reabsorption (reuptake) of serotonin into the presynaptic neuron, increasing the availability of serotonin in the synapse to interact with postsynaptic receptors. SSRIs are commonly used as antidepressants and include medications such as fluoxetine, sertraline, and citalopram.
2. Serotonin-Norepinephrine Reuptake Inhibitors (SNRIs): These drugs block the reabsorption of both serotonin and norepinephrine into the presynaptic neuron, increasing the availability of these neurotransmitters in the synapse. SNRIs are also used as antidepressants and include medications such as venlafaxine and duloxetine.
3. Serotonin Receptor Agonists: These drugs bind to and activate serotonin receptors, mimicking the effects of serotonin. They are used for various indications, including migraine prevention (e.g., sumatriptan) and Parkinson's disease (e.g., pramipexole).
4. Serotonin Receptor Antagonists: These drugs block serotonin receptors, preventing the effects of serotonin. They are used for various indications, including nausea and vomiting (e.g., ondansetron) and as mood stabilizers in bipolar disorder (e.g., olanzapine).
5. Serotonin Synthesis Inhibitors: These drugs block the enzymatic synthesis of serotonin, reducing its availability in the brain. They are used as antidepressants and include medications such as monoamine oxidase inhibitors (MAOIs) like phenelzine and tranylcypromine.

It's important to note that while these drugs all affect serotonin, they have different mechanisms of action and are used for various indications. It's essential to consult a healthcare professional before starting any new medication.

Phenethylamines are a class of organic compounds that share a common structural feature, which is a phenethyl group (a phenyl ring bonded to an ethylamine chain). In the context of pharmacology and neuroscience, "phenethylamines" often refers to a specific group of psychoactive drugs, including stimulants like amphetamine and mescaline, a classic psychedelic. These compounds exert their effects by modulating the activity of neurotransmitters in the brain, such as dopamine, norepinephrine, and serotonin. It is important to note that many phenethylamines have potential for abuse and are controlled substances.

Apomorphine is a non-selective dopamine receptor agonist, which means that it activates dopamine receptors in the brain. It has a high affinity for D1 and D2 dopamine receptors and is used medically to treat Parkinson's disease, particularly in cases of severe or intractable motor fluctuations.

Apomorphine can be administered subcutaneously (under the skin) as a solution or as a sublingual (under the tongue) film. It works by stimulating dopamine receptors in the brain, which helps to reduce the symptoms of Parkinson's disease such as stiffness, tremors, and difficulty with movement.

In addition to its use in Parkinson's disease, apomorphine has also been investigated for its potential therapeutic benefits in other neurological disorders, including alcohol use disorder and drug addiction. However, more research is needed to establish its safety and efficacy in these conditions.

A drug interaction is the effect of combining two or more drugs, or a drug and another substance (such as food or alcohol), which can alter the effectiveness or side effects of one or both of the substances. These interactions can be categorized as follows:

1. Pharmacodynamic interactions: These occur when two or more drugs act on the same target organ or receptor, leading to an additive, synergistic, or antagonistic effect. For example, taking a sedative and an antihistamine together can result in increased drowsiness due to their combined depressant effects on the central nervous system.
2. Pharmacokinetic interactions: These occur when one drug affects the absorption, distribution, metabolism, or excretion of another drug. For example, taking certain antibiotics with grapefruit juice can increase the concentration of the antibiotic in the bloodstream, leading to potential toxicity.
3. Food-drug interactions: Some drugs may interact with specific foods, affecting their absorption, metabolism, or excretion. An example is the interaction between warfarin (a blood thinner) and green leafy vegetables, which can increase the risk of bleeding due to enhanced vitamin K absorption from the vegetables.
4. Drug-herb interactions: Some herbal supplements may interact with medications, leading to altered drug levels or increased side effects. For instance, St. John's Wort can decrease the effectiveness of certain antidepressants and oral contraceptives by inducing their metabolism.
5. Drug-alcohol interactions: Alcohol can interact with various medications, causing additive sedative effects, impaired judgment, or increased risk of liver damage. For example, combining alcohol with benzodiazepines or opioids can lead to dangerous levels of sedation and respiratory depression.

It is essential for healthcare providers and patients to be aware of potential drug interactions to minimize adverse effects and optimize treatment outcomes.

Biogenic amine receptors are a type of cell surface receptor that bind and respond to biogenic amines, which are naturally occurring compounds that function as neurotransmitters or hormones in the human body. These receptors play crucial roles in various physiological processes, including regulation of mood, appetite, sleep, and cognition.

Examples of biogenic amines include:

1. Dopamine (DA): Dopamine receptors are involved in motor control, reward processing, and motivation. They are divided into two main classes: D1-like (D1 and D5) and D2-like (D2, D3, and D4).
2. Serotonin (5-HT): Serotonin receptors regulate mood, appetite, sleep, and pain perception. There are seven distinct families of serotonin receptors (5-HT1 to 5-HT7), with multiple subtypes within each family.
3. Norepinephrine (NE): Also known as noradrenaline, norepinephrine receptors play a role in the "fight or flight" response, attention, and arousal. They are divided into two main classes: α-adrenergic (α1 and α2) and β-adrenergic (β1, β2, and β3).
4. Histamine (HA): Histamine receptors regulate allergic responses, wakefulness, and appetite. There are four types of histamine receptors (H1 to H4), with distinct functions and signaling pathways.
5. Acetylcholine (ACh): While not a biogenic amine, acetylcholine is often included in this category due to its similar role as a neurotransmitter. Acetylcholine receptors are involved in learning, memory, and muscle contraction. They can be further divided into muscarinic (M1-M5) and nicotinic (α and β subunits) receptor classes.

Biogenic amine receptors typically function through G protein-coupled receptor (GPCR) signaling pathways, although some can also activate ion channels directly. Dysregulation of biogenic amine systems has been implicated in various neurological and psychiatric disorders, such as Parkinson's disease, depression, and schizophrenia.

Phenylpropanolamine is a decongestant and appetite suppressant that has been used in over-the-counter and prescription medications. It works by narrowing blood vessels in the nose, which can help to relieve nasal congestion. As an appetite suppressant, it is thought to work by affecting certain chemicals in the brain that control appetite.

However, phenylpropanolamine has been associated with an increased risk of hemorrhagic stroke (bleeding in the brain) and other cardiovascular events, particularly in women who are otherwise healthy but have a history of high blood pressure or smoking. As a result, the U.S. Food and Drug Administration (FDA) advised manufacturers to stop selling over-the-counter products containing phenylpropanolamine in 2005.

It is important to note that this substance should only be used under the supervision of a healthcare professional, and individuals should always follow their doctor's instructions carefully when taking any medication.

Serotonin, also known as 5-hydroxytryptamine (5-HT), is a monoamine neurotransmitter that is found primarily in the gastrointestinal (GI) tract, blood platelets, and the central nervous system (CNS) of humans and other animals. It is produced by the conversion of the amino acid tryptophan to 5-hydroxytryptophan (5-HTP), and then to serotonin.

In the CNS, serotonin plays a role in regulating mood, appetite, sleep, memory, learning, and behavior, among other functions. It also acts as a vasoconstrictor, helping to regulate blood flow and blood pressure. In the GI tract, it is involved in peristalsis, the contraction and relaxation of muscles that moves food through the digestive system.

Serotonin is synthesized and stored in serotonergic neurons, which are nerve cells that use serotonin as their primary neurotransmitter. These neurons are found throughout the brain and spinal cord, and they communicate with other neurons by releasing serotonin into the synapse, the small gap between two neurons.

Abnormal levels of serotonin have been linked to a variety of disorders, including depression, anxiety, schizophrenia, and migraines. Medications that affect serotonin levels, such as selective serotonin reuptake inhibitors (SSRIs), are commonly used to treat these conditions.

Raclopride is not a medical condition but a drug that belongs to the class of dopamine receptor antagonists. It's primarily used in research and diagnostic settings as a radioligand in positron emission tomography (PET) scans to visualize and measure the distribution and availability of dopamine D2 and D3 receptors in the brain.

In simpler terms, Raclopride is a compound that can be labeled with a radioactive isotope and then introduced into the body to track the interaction between the radioligand and specific receptors (in this case, dopamine D2 and D3 receptors) in the brain. This information can help researchers and clinicians better understand neurochemical processes and disorders related to dopamine dysfunction, such as Parkinson's disease, schizophrenia, and drug addiction.

It is important to note that Raclopride is not used as a therapeutic agent in clinical practice due to its short half-life and the potential for side effects associated with dopamine receptor blockade.

Self-administration, in the context of medicine and healthcare, refers to the act of an individual administering medication or treatment to themselves. This can include various forms of delivery such as oral medications, injections, or topical treatments. It is important that individuals who self-administer are properly trained and understand the correct dosage, timing, and technique to ensure safety and effectiveness. Self-administration promotes independence, allows for timely treatment, and can improve overall health outcomes.

Adrenergic agents are a class of drugs that bind to and activate adrenergic receptors, which are cell surface receptors found in the nervous system and other tissues. These receptors are activated by neurotransmitters such as norepinephrine and epinephrine (also known as adrenaline), which are released by the sympathetic nervous system in response to stress or excitement.

Adrenergic agents can be classified based on their mechanism of action and the specific receptors they bind to. There are two main types of adrenergic receptors: alpha and beta receptors, each with several subtypes. Some adrenergic agents bind to both alpha and beta receptors, while others are selective for one or the other.

Adrenergic agents have a wide range of therapeutic uses, including the treatment of asthma, cardiovascular diseases, glaucoma, and neurological disorders. They can also be used as diagnostic tools to test the function of the sympathetic nervous system. Some examples of adrenergic agents include:

* Alpha-agonists: These drugs bind to alpha receptors and cause vasoconstriction (narrowing of blood vessels), which can be useful in the treatment of hypotension (low blood pressure) or nasal congestion. Examples include phenylephrine and oxymetazoline.
* Alpha-antagonists: These drugs block the action of alpha receptors, leading to vasodilation (widening of blood vessels) and a decrease in blood pressure. Examples include prazosin and doxazosin.
* Beta-agonists: These drugs bind to beta receptors and cause bronchodilation (opening of the airways), increased heart rate, and increased force of heart contractions. They are used in the treatment of asthma, chronic obstructive pulmonary disease (COPD), and other respiratory disorders. Examples include albuterol and salmeterol.
* Beta-antagonists: These drugs block the action of beta receptors, leading to a decrease in heart rate, blood pressure, and bronchodilation. They are used in the treatment of hypertension, angina (chest pain), and heart failure. Examples include metoprolol and atenolol.
* Nonselective alpha- and beta-antagonists: These drugs block both alpha and beta receptors and are used in the treatment of hypertension, angina, and heart failure. Examples include labetalol and carvedilol.

Barbiturates are a class of drugs that act as central nervous system depressants, which means they slow down the activity of the brain and nerves. They were commonly used in the past to treat conditions such as anxiety, insomnia, and seizures, but their use has declined due to the risk of addiction, abuse, and serious side effects. Barbiturates can also be used for surgical anesthesia and as a treatment for barbiturate or pentobarbital overdose.

Barbiturates work by enhancing the activity of the neurotransmitter gamma-aminobutyric acid (GABA) in the brain, which results in sedation, hypnosis, and anticonvulsant effects. However, at higher doses, barbiturates can cause respiratory depression, coma, and even death.

Some examples of barbiturates include pentobarbital, phenobarbital, secobarbital, and amobarbital. These drugs are usually available in the form of tablets, capsules, or injectable solutions. It is important to note that barbiturates should only be used under the supervision of a healthcare professional, as they carry a high risk of dependence and abuse.

"Long-Evans" is a strain of laboratory rats commonly used in scientific research. They are named after their developers, the scientists Long and Evans. This strain is albino, with a brownish-black hood over their eyes and ears, and they have an agouti (salt-and-pepper) color on their backs. They are often used as a model organism due to their size, ease of handling, and genetic similarity to humans. However, I couldn't find any specific medical definition related to "Long-Evans rats" as they are not a medical condition or disease.

Reserpine is an alkaloid derived from the Rauwolfia serpentina plant, which has been used in traditional medicine for its sedative and hypotensive effects. In modern medicine, reserpine is primarily used to treat hypertension (high blood pressure) due to its ability to lower both systolic and diastolic blood pressure.

Reserpine works by depleting catecholamines, including norepinephrine, epinephrine, and dopamine, from nerve terminals in the sympathetic nervous system. This leads to a decrease in peripheral vascular resistance and heart rate, ultimately resulting in reduced blood pressure.

Reserpine is available in various forms, such as tablets or capsules, and is typically administered orally. Common side effects include nasal congestion, dizziness, sedation, and gastrointestinal disturbances like diarrhea and nausea. Long-term use of reserpine may also lead to depression in some individuals. Due to its potential for causing depression, other antihypertensive medications are often preferred over reserpine when possible.

Pargyline is an antihypertensive drug and a irreversible monoamine oxidase inhibitor (MAOI) of type B. It works by blocking the breakdown of certain chemicals in the brain, such as neurotransmitters, which can help improve mood and behavior in people with depression.

Pargyline is not commonly used as a first-line treatment for depression due to its potential for serious side effects, including interactions with certain foods and medications that can lead to dangerously high blood pressure. It is also associated with a risk of serotonin syndrome when taken with selective serotonin reuptake inhibitors (SSRIs) or other drugs that increase serotonin levels in the brain.

Pargyline is available only through a prescription and should be used under the close supervision of a healthcare provider.

Chlorfenvinphos is an organophosphate insecticide that has been used to control a wide variety of pests in agriculture, horticulture, and animal husbandry. It functions by inhibiting the enzyme acetylcholinesterase, which leads to an accumulation of the neurotransmitter acetylcholine and results in symptoms such as muscle twitching, tremors, convulsions, and eventually respiratory failure.

Chlorfenvinphos is highly toxic to both mammals and birds, and it can also have harmful effects on aquatic organisms. It has been banned or restricted in many countries due to its environmental persistence and potential health risks to humans. Exposure to chlorfenvinphos can occur through inhalation, skin contact, or ingestion, and symptoms of poisoning may include nausea, vomiting, diarrhea, abdominal cramps, headache, dizziness, and respiratory distress. Chronic exposure has been linked to neurological effects such as memory loss, decreased cognitive function, and peripheral neuropathy.

Medically, hair is defined as a threadlike structure that grows from the follicles found in the skin of mammals. It is primarily made up of a protein called keratin and consists of three parts: the medulla (the innermost part or core), the cortex (middle layer containing keratin filaments) and the cuticle (outer layer of overlapping scales).

Hair growth occurs in cycles, with each cycle consisting of a growth phase (anagen), a transitional phase (catagen), and a resting phase (telogen). The length of hair is determined by the duration of the anagen phase.

While hair plays a crucial role in protecting the skin from external factors like UV radiation, temperature changes, and physical damage, it also serves as an essential aspect of human aesthetics and identity.

Psychotropic drugs, also known as psychoactive drugs, are a class of medications that affect the function of the central nervous system, leading to changes in consciousness, perception, mood, cognition, or behavior. These drugs work by altering the chemical neurotransmitters in the brain, such as dopamine, serotonin, and norepinephrine, which are involved in regulating mood, thought, and behavior.

Psychotropic drugs can be classified into several categories based on their primary therapeutic effects, including:

1. Antipsychotic drugs: These medications are used to treat psychosis, schizophrenia, and other related disorders. They work by blocking dopamine receptors in the brain, which helps reduce hallucinations, delusions, and disordered thinking.
2. Antidepressant drugs: These medications are used to treat depression, anxiety disorders, and some chronic pain conditions. They work by increasing the availability of neurotransmitters such as serotonin, norepinephrine, or dopamine in the brain, which helps improve mood and reduce anxiety.
3. Mood stabilizers: These medications are used to treat bipolar disorder and other mood disorders. They help regulate the ups and downs of mood swings and can also be used as adjunctive treatment for depression and anxiety.
4. Anxiolytic drugs: Also known as anti-anxiety medications, these drugs are used to treat anxiety disorders, panic attacks, and insomnia. They work by reducing the activity of neurotransmitters such as GABA, which can help reduce anxiety and promote relaxation.
5. Stimulant drugs: These medications are used to treat attention deficit hyperactivity disorder (ADHD) and narcolepsy. They work by increasing the availability of dopamine and norepinephrine in the brain, which helps improve focus, concentration, and alertness.

It is important to note that psychotropic drugs can have significant side effects and should only be used under the close supervision of a qualified healthcare provider.

A Fluorescence Polarization Immunoassay (FPIA) is a type of biochemical test used for the detection and quantitation of various analytes, such as drugs, hormones, or proteins, in a sample. It is based on the principle of fluorescence polarization, which measures the rotation of molecules in solution.

In an FPIA, the sample is mixed with a fluorescent tracer that binds specifically to the analyte of interest. When the mixture is excited with plane-polarized light, the fluorescent tracer emits light that retains its polarization if it remains bound to the large complex (analyte+tracer). However, if the tracer is not bound to the analyte and is free to rotate in solution, the emitted light becomes depolarized.

The degree of polarization of the emitted light is then measured and used to determine the amount of analyte present in the sample. Higher concentrations of analyte result in a higher degree of polarization, as more tracer molecules are bound and less likely to rotate.

FPIAs offer several advantages over other types of immunoassays, including simplicity, speed, and sensitivity. They are commonly used in clinical laboratories for the detection of drugs of abuse, therapeutic drugs, and hormones.

A startle reaction is a natural, defensive response to an unexpected stimulus that is characterized by a sudden contraction of muscles, typically in the face, neck, and arms. It's a reflexive action that occurs involuntarily and is mediated by the brainstem. The startle reaction can be observed in many different species, including humans, and is thought to have evolved as a protective mechanism to help organisms respond quickly to potential threats. In addition to the muscle contraction, the startle response may also include other physiological changes such as an increase in heart rate and blood pressure.

Specific gravity is a term used in medicine, particularly in the context of urinalysis and other bodily fluid analysis. It refers to the ratio of the density (mass of a substance per unit volume) of a sample to the density of a reference substance, usually water. At body temperature, this is expressed as:

Specific gravity = Density of sample / Density of water at 37 degrees Celsius

In urinalysis, specific gravity is used to help evaluate renal function and hydration status. It can indicate whether the kidneys are adequately concentrating or diluting the urine. A lower specific gravity (closer to 1) may suggest overhydration or dilute urine, while a higher specific gravity (greater than 1) could indicate dehydration or concentrated urine. However, specific gravity should be interpreted in conjunction with other urinalysis findings and clinical context for accurate assessment.

Locomotion, in a medical context, refers to the ability to move independently and change location. It involves the coordinated movement of the muscles, bones, and nervous system that enables an individual to move from one place to another. This can include walking, running, jumping, or using assistive devices such as wheelchairs or crutches. Locomotion is a fundamental aspect of human mobility and is often assessed in medical evaluations to determine overall health and functioning.

Selegiline is a selective, irreversible MAO-B inhibitor, which is primarily used in the clinical management of Parkinson's disease. It works by blocking the action of monoamine oxidase B (MAO-B), an enzyme responsible for breaking down dopamine, a neurotransmitter involved in movement regulation. By inhibiting MAO-B, selegiline increases the availability of dopamine in the brain, thereby helping to alleviate symptoms of Parkinson's disease such as stiffness, tremors, and spasms.

Selegiline is also available under the brand name Eldepryl, Zelapar, and Emsam. In addition to its use in Parkinson's disease, selegiline has been explored for its potential benefits in treating depression, dementia, and other neurological disorders. However, its use in these conditions is still considered off-label and requires careful consideration of the potential risks and benefits.

It is important to note that MAO inhibitors like selegiline can have serious interactions with certain foods and medications, particularly those containing tyramine, which can lead to a dangerous increase in blood pressure (hypertensive crisis). Therefore, it is crucial to follow strict dietary restrictions and medication guidelines when taking selegiline or any other MAO inhibitor.

"Intraperitoneal injection" is a medical term that refers to the administration of a substance or medication directly into the peritoneal cavity, which is the space between the lining of the abdominal wall and the organs contained within it. This type of injection is typically used in clinical settings for various purposes, such as delivering chemotherapy drugs, anesthetics, or other medications directly to the abdominal organs.

The procedure involves inserting a needle through the abdominal wall and into the peritoneal cavity, taking care to avoid any vital structures such as blood vessels or nerves. Once the needle is properly positioned, the medication can be injected slowly and carefully to ensure even distribution throughout the cavity.

It's important to note that intraperitoneal injections are typically reserved for situations where other routes of administration are not feasible or effective, as they carry a higher risk of complications such as infection, bleeding, or injury to surrounding organs. As with any medical procedure, it should only be performed by trained healthcare professionals under appropriate clinical circumstances.

Dopamine D1 receptors are a type of G protein-coupled receptor that bind to the neurotransmitter dopamine. They are classified as D1-like receptors, along with D5 receptors, and are activated by dopamine through a stimulatory G protein (Gs).

D1 receptors are widely expressed in the central nervous system, including the striatum, prefrontal cortex, hippocampus, and amygdala. They play important roles in various physiological functions, such as movement control, motivation, reward processing, working memory, and cognition.

Activation of D1 receptors leads to increased levels of intracellular cyclic adenosine monophosphate (cAMP) and activation of protein kinase A (PKA), which in turn modulate the activity of various downstream signaling pathways. Dysregulation of dopamine D1 receptor function has been implicated in several neurological and psychiatric disorders, including Parkinson's disease, schizophrenia, attention deficit hyperactivity disorder (ADHD), and drug addiction.

Dopamine receptors are a type of G protein-coupled receptor that bind to and respond to the neurotransmitter dopamine. There are five subtypes of dopamine receptors (D1-D5), which are classified into two families based on their structure and function: D1-like (D1 and D5) and D2-like (D2, D3, and D4).

Dopamine receptors play a crucial role in various physiological processes, including movement, motivation, reward, cognition, emotion, and neuroendocrine regulation. They are widely distributed throughout the central nervous system, with high concentrations found in the basal ganglia, limbic system, and cortex.

Dysfunction of dopamine receptors has been implicated in several neurological and psychiatric disorders, such as Parkinson's disease, schizophrenia, attention deficit hyperactivity disorder (ADHD), drug addiction, and depression. Therefore, drugs targeting dopamine receptors have been developed for the treatment of these conditions.

Sympathomimetic drugs are substances that mimic or stimulate the actions of the sympathetic nervous system. The sympathetic nervous system is one of the two divisions of the autonomic nervous system, which regulates various automatic physiological functions in the body. The sympathetic nervous system's primary function is to prepare the body for the "fight-or-flight" response, which includes increasing heart rate, blood pressure, respiratory rate, and metabolism while decreasing digestive activity.

Sympathomimetic drugs can exert their effects through various mechanisms, including directly stimulating adrenergic receptors (alpha and beta receptors) or indirectly causing the release of norepinephrine and epinephrine from nerve endings. These drugs are used in various clinical settings to treat conditions such as asthma, nasal congestion, low blood pressure, and attention deficit hyperactivity disorder (ADHD). Examples of sympathomimetic drugs include epinephrine, norepinephrine, dopamine, dobutamine, albuterol, pseudoephedrine, and methylphenidate.

It is important to note that sympathomimetic drugs can also have adverse effects, particularly when used in high doses or in individuals with certain medical conditions. These adverse effects may include anxiety, tremors, palpitations, hypertension, arrhythmias, and seizures. Therefore, these medications should be used under the close supervision of a healthcare provider.

Quinpirole is not a medical condition or disease, but rather a synthetic compound used in research and medicine. It's a selective agonist for the D2 and D3 dopamine receptors, which means it binds to and activates these receptors, mimicking the effects of dopamine, a neurotransmitter involved in various physiological processes such as movement, motivation, reward, and cognition.

Quinpirole is used primarily in preclinical research to study the role of dopamine receptors in different neurological conditions, including Parkinson's disease, schizophrenia, drug addiction, and others. It helps researchers understand how dopamine systems work and contributes to the development of new therapeutic strategies for these disorders.

It is important to note that quinpirole is not used as a medication in humans or animals but rather as a research tool in laboratory settings.

Tyramine is not a medical condition but a naturally occurring compound called a biogenic amine, which is formed from the amino acid tyrosine during the fermentation or decay of certain foods. Medically, tyramine is significant because it can interact with certain medications, particularly monoamine oxidase inhibitors (MAOIs), used to treat depression and other conditions.

The interaction between tyramine and MAOIs can lead to a hypertensive crisis, a rapid and severe increase in blood pressure, which can be life-threatening if not treated promptly. Therefore, individuals taking MAOIs are often advised to follow a low-tyramine diet, avoiding foods high in tyramine, such as aged cheeses, cured meats, fermented foods, and some types of beer and wine.

Biogenic monoamines are a type of neurotransmitter, which are chemical messengers that transmit signals in the brain and other parts of the nervous system. They are called "biogenic" because they are derived from biological substances, and "monoamines" because they contain one amine group (-NH2) and are derived from the aromatic amino acids: tryptophan, tyrosine, and phenylalanine.

Examples of biogenic monoamines include:

1. Serotonin (5-hydroxytryptamine or 5-HT): synthesized from the amino acid tryptophan and plays a crucial role in regulating mood, appetite, sleep, memory, and learning.
2. Dopamine: formed from tyrosine and is involved in reward, motivation, motor control, and reinforcement of behavior.
3. Norepinephrine (noradrenaline): also derived from tyrosine and functions as a neurotransmitter and hormone that modulates attention, arousal, and stress responses.
4. Epinephrine (adrenaline): synthesized from norepinephrine and serves as a crucial hormone and neurotransmitter in the body's fight-or-flight response to stress or danger.
5. Histamine: produced from the amino acid histidine, it acts as a neurotransmitter and mediates allergic reactions, immune responses, and regulates wakefulness and appetite.

Imbalances in biogenic monoamines have been linked to various neurological and psychiatric disorders, such as depression, anxiety, Parkinson's disease, and schizophrenia. Therefore, medications that target these neurotransmitters, like selective serotonin reuptake inhibitors (SSRIs) for depression or levodopa for Parkinson's disease, are often used in the treatment of these conditions.

Exploratory behavior refers to the actions taken by an individual to investigate and gather information about their environment. This type of behavior is often driven by curiosity and a desire to understand new or unfamiliar situations, objects, or concepts. In a medical context, exploratory behavior may refer to a patient's willingness to learn more about their health condition, try new treatments, or engage in self-care activities. It can also refer to the behaviors exhibited by young children as they explore their world and develop their cognitive and motor skills. Exploratory behavior is an important aspect of learning and development, and it can have a positive impact on overall health and well-being.

Narcolepsy is a chronic neurological disorder that affects the control of sleep and wakefulness. It's characterized by excessive daytime sleepiness (EDS), where people experience sudden, uncontrollable episodes of falling asleep during the day. These "sleep attacks" can occur at any time - while working, talking, eating, or even driving.

In addition to EDS, narcolepsy often includes cataplexy, a condition that causes loss of muscle tone, leading to weakness and sometimes collapse, often triggered by strong emotions like laughter or surprise. Other common symptoms are sleep paralysis (a temporary inability to move or speak while falling asleep or waking up), vivid hallucinations during the transitions between sleep and wakefulness, and fragmented nighttime sleep.

The exact cause of narcolepsy is not fully understood, but it's believed to involve genetic and environmental factors, as well as problems with certain neurotransmitters in the brain, such as hypocretin/orexin, which regulate sleep-wake cycles. Narcolepsy can significantly impact a person's quality of life, making it essential to seek medical attention for proper diagnosis and management.

Classical conditioning is a type of learning process that occurs when two stimuli are repeatedly paired together, leading to an association between them. This concept was first introduced by Ivan Pavlov, a Russian physiologist, in his studies on classical conditioning in the late 19th and early 20th centuries.

In classical conditioning, there are typically two types of stimuli involved: the unconditioned stimulus (US) and the neutral stimulus (NS). The US is a stimulus that naturally triggers a response, known as the unconditioned response (UR), in an organism. For example, food is an US that triggers salivation, which is the UR, in dogs.

The NS, on the other hand, is a stimulus that does not initially trigger any response in the organism. However, when the NS is repeatedly paired with the US, it becomes a conditioned stimulus (CS) and begins to elicit a conditioned response (CR). The CR is similar to the UR but is triggered by the CS instead of the US.

For example, if Pavlov repeatedly rang a bell (NS) just before presenting food (US) to a dog, the dog would eventually start salivating (CR) in response to the bell (CS) even when food was not presented. This is an example of classical conditioning.

Classical conditioning has been widely studied and is believed to play a role in various physiological processes, such as learning, memory, and emotion regulation. It has also been used in various applications, including behavioral therapy and advertising.

Stereoisomerism is a type of isomerism (structural arrangement of atoms) in which molecules have the same molecular formula and sequence of bonded atoms, but differ in the three-dimensional orientation of their atoms in space. This occurs when the molecule contains asymmetric carbon atoms or other rigid structures that prevent free rotation, leading to distinct spatial arrangements of groups of atoms around a central point. Stereoisomers can have different chemical and physical properties, such as optical activity, boiling points, and reactivities, due to differences in their shape and the way they interact with other molecules.

There are two main types of stereoisomerism: enantiomers (mirror-image isomers) and diastereomers (non-mirror-image isomers). Enantiomers are pairs of stereoisomers that are mirror images of each other, but cannot be superimposed on one another. Diastereomers, on the other hand, are non-mirror-image stereoisomers that have different physical and chemical properties.

Stereoisomerism is an important concept in chemistry and biology, as it can affect the biological activity of molecules, such as drugs and natural products. For example, some enantiomers of a drug may be active, while others are inactive or even toxic. Therefore, understanding stereoisomerism is crucial for designing and synthesizing effective and safe drugs.

Monoamine oxidase inhibitors (MAOIs) are a class of drugs that work by blocking the action of monoamine oxidase, an enzyme found in the brain and other organs of the body. This enzyme is responsible for breaking down certain neurotransmitters, such as serotonin, dopamine, and norepinephrine, which are chemicals that transmit signals in the brain.

By inhibiting the action of monoamine oxidase, MAOIs increase the levels of these neurotransmitters in the brain, which can help to alleviate symptoms of depression and other mood disorders. However, MAOIs also affect other chemicals in the body, including tyramine, a substance found in some foods and beverages, as well as certain medications. As a result, MAOIs can have serious side effects and interactions with other substances, making them a less commonly prescribed class of antidepressants than other types of drugs.

MAOIs are typically used as a last resort when other treatments for depression have failed, due to their potential for dangerous interactions and side effects. They require careful monitoring and dosage adjustment by a healthcare provider, and patients must follow strict dietary restrictions while taking them.

Phencyclidine (PCP) is a dissociative drug that was originally developed as an intravenous anesthetic in the 1950s. It can lead to distortions of time, space and body image, hallucinations, and a sense of physical invulnerability.

It can also cause numbness, loss of coordination, and aggressive behavior. High doses can lead to seizures, coma, and death. Long-term use can lead to memory loss, difficulties with speech and thinking, and mental health issues such as depression and suicidal thoughts. It is classified as a Schedule II drug in the United States, indicating it has a high potential for abuse but also an accepted medical use.

Salicylamides are organic compounds that consist of a salicylic acid molecule (a type of phenolic acid) linked to an amide group. They are derivatives of salicylic acid and are known for their analgesic, anti-inflammatory, and antipyretic properties. Salicylamides have been used in various pharmaceutical and therapeutic applications, including the treatment of pain, fever, and inflammation. However, they have largely been replaced by other compounds such as acetylsalicylic acid (aspirin) due to their lower potency and potential side effects.

An immunoassay is a biochemical test that measures the presence or concentration of a specific protein, antibody, or antigen in a sample using the principles of antibody-antigen reactions. It is commonly used in clinical laboratories to diagnose and monitor various medical conditions such as infections, hormonal disorders, allergies, and cancer.

Immunoassays typically involve the use of labeled reagents, such as enzymes, radioisotopes, or fluorescent dyes, that bind specifically to the target molecule. The amount of label detected is proportional to the concentration of the target molecule in the sample, allowing for quantitative analysis.

There are several types of immunoassays, including enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), fluorescence immunoassay (FIA), and chemiluminescent immunoassay (CLIA). Each type has its own advantages and limitations, depending on the sensitivity, specificity, and throughput required for a particular application.

Euphoria is a medical term that refers to an state of intense happiness and well-being, often exaggerated or irrational in context. It is a heightened state of pleasure or excitement, sometimes reaching levels of ecstasy. Euphoria can be a symptom of certain medical conditions, such as manic episodes associated with bipolar disorder, or it can be a side effect of certain drugs, including some prescription medications and illegal substances.

In a clinical setting, euphoria is often assessed using rating scales to help diagnose and monitor the severity of various mental health disorders. It's important to note that while euphoria can be a positive experience for some individuals, it can also have negative consequences, particularly when it leads to impaired judgment or risky behaviors.

Phentermine is a defined in the medical field as a psychostimulant medication that is primarily used for short-term weight management. It acts as an appetite suppressant and has sympathomimetic properties, which means it stimulates the sympathetic nervous system, leading to increased heart rate and blood pressure.

Phentermine is available in various forms, including tablets, capsules, and orally disintegrating tablets. It is typically prescribed for individuals with a body mass index (BMI) of 30 or higher, or for those with a BMI of 27 or higher who have weight-related medical conditions such as high blood pressure, diabetes, or high cholesterol.

It's important to note that phentermine is intended for use in conjunction with a reduced-calorie diet and increased physical activity. It should not be used as a sole means of weight loss, and its long-term effectiveness and safety have not been established. Additionally, phentermine can be habit-forming and may cause dependence, so it should only be used under the close supervision of a healthcare provider.

A reinforcement schedule is a concept in behavioral psychology that refers to the timing and pattern of rewards or reinforcements provided in response to certain behaviors. It is used to shape, maintain, or strengthen specific behaviors in individuals. There are several types of reinforcement schedules, including:

1. **Fixed Ratio (FR):** A reward is given after a fixed number of responses. For example, a salesperson might receive a bonus for every 10 sales they make.
2. **Variable Ratio (VR):** A reward is given after an unpredictable number of responses. This schedule is commonly used in gambling, as the uncertainty of when a reward (winning) will occur keeps the individual engaged and motivated to continue the behavior.
3. **Fixed Interval (FI):** A reward is given after a fixed amount of time has passed since the last reward, regardless of the number of responses during that time. For example, an employee might receive a paycheck every two weeks, regardless of how many tasks they completed during that period.
4. **Variable Interval (VI):** A reward is given after an unpredictable amount of time has passed since the last reward, regardless of the number of responses during that time. This schedule can be observed in foraging behavior, where animals search for food at irregular intervals.
5. **Combined schedules:** Reinforcement schedules can also be combined to create more complex patterns, such as a fixed ratio followed by a variable interval (FR-VI) or a variable ratio followed by a fixed interval (VR-FI).

Understanding reinforcement schedules is essential for developing effective behavioral interventions in various settings, including healthcare, education, and rehabilitation.

Catalepsy is a medical condition characterized by a trance-like state, with reduced sensitivity to pain and external stimuli, muscular rigidity, and fixed postures. In this state, the person's body may maintain any position in which it is placed for a long time, and there is often a decreased responsiveness to social cues or communication attempts.

Catalepsy can be a symptom of various medical conditions, including neurological disorders such as epilepsy, Parkinson's disease, or brain injuries. It can also occur in the context of mental health disorders, such as severe depression, catatonic schizophrenia, or dissociative identity disorder.

In some cases, catalepsy may be induced intentionally through hypnosis or other forms of altered consciousness practices. However, when it occurs spontaneously or as a symptom of an underlying medical condition, it can be a serious concern and requires medical evaluation and treatment.

The putamen is a round, egg-shaped structure that is a part of the basal ganglia, located in the forebrain. It is situated laterally to the globus pallidus and medially to the internal capsule. The putamen plays a crucial role in regulating movement and is involved in various functions such as learning, motivation, and habit formation.

It receives input from the cerebral cortex via the corticostriatal pathway and sends output to the globus pallidus and substantia nigra pars reticulata, which are also part of the basal ganglia circuitry. The putamen is heavily innervated by dopaminergic neurons from the substantia nigra pars compacta, and degeneration of these neurons in Parkinson's disease leads to a significant reduction in dopamine levels in the putamen, resulting in motor dysfunction.

Narcotics, in a medical context, are substances that induce sleep, relieve pain, and suppress cough. They are often used for anesthesia during surgical procedures. Narcotics are derived from opium or its synthetic substitutes and include drugs such as morphine, codeine, fentanyl, oxycodone, and hydrocodone. These drugs bind to specific receptors in the brain and spinal cord, reducing the perception of pain and producing a sense of well-being. However, narcotics can also produce physical dependence and addiction, and their long-term use can lead to tolerance, meaning that higher doses are required to achieve the same effect. Narcotics are classified as controlled substances due to their potential for abuse and are subject to strict regulations.

"Cocaine-Related Disorders" is a term used in the medical and psychiatric fields to refer to a group of conditions related to the use of cocaine, a powerful stimulant drug. These disorders are classified and diagnosed based on the criteria outlined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5), published by the American Psychiatric Association.

The two main categories of Cocaine-Related Disorders are:

1. Cocaine Use Disorder: This disorder is characterized by a problematic pattern of cocaine use leading to clinically significant impairment or distress, as manifested by at least two symptoms within a 12-month period. These symptoms may include using larger amounts of cocaine over a longer period than intended, persistent desire or unsuccessful efforts to cut down or control cocaine use, spending a great deal of time obtaining, using, or recovering from the effects of cocaine, and continued use despite physical or psychological problems caused or exacerbated by cocaine.
2. Cocaine-Induced Disorders: These disorders are directly caused by the acute effects of cocaine intoxication or withdrawal. They include:
* Cocaine Intoxication: Presents with a reversible syndrome due to recent use of cocaine, characterized by euphoria, increased energy, and psychomotor agitation. It may also cause elevated heart rate, blood pressure, and body temperature, as well as pupillary dilation.
* Cocaine Withdrawal: Occurs when an individual who has been using cocaine heavily for a prolonged period abruptly stops or significantly reduces their use. Symptoms include depressed mood, fatigue, increased appetite, vivid and unpleasant dreams, and insomnia.

Cocaine-Related Disorders can have severe negative consequences on an individual's physical health, mental wellbeing, and social functioning. They often require professional treatment to manage and overcome.

Biogenic amines are organic compounds that are derived from the metabolic pathways of various biological organisms, including humans. They are formed by the decarboxylation of amino acids, which are the building blocks of proteins. Some examples of biogenic amines include histamine, serotonin, dopamine, and tyramine.

Histamine is a biogenic amine that plays an important role in the immune system's response to foreign invaders, such as allergens. It is also involved in regulating stomach acid production and sleep-wake cycles. Serotonin is another biogenic amine that acts as a neurotransmitter, transmitting signals between nerve cells in the brain. It is involved in regulating mood, appetite, and sleep.

Dopamine is a biogenic amine that functions as a neurotransmitter and is involved in reward and pleasure pathways in the brain. Tyramine is a biogenic amine that is found in certain foods, such as aged cheeses and fermented soy products. It can cause an increase in blood pressure when consumed in large quantities.

Biogenic amines can have various effects on the body, depending on their type and concentration. In general, they play important roles in many physiological processes, but high levels of certain biogenic amines can be harmful and may cause symptoms such as headache, nausea, and hypertension.

Tranylcypromine is a type of antidepressant known as a non-selective, irreversible monoamine oxidase inhibitor (MAOI). It works by blocking the action of monoamine oxidase, an enzyme that breaks down certain neurotransmitters (chemical messengers) in the brain such as serotonin, dopamine, and noradrenaline. This leads to an increase in the levels of these neurotransmitters in the brain, which can help improve mood and alleviate symptoms of depression.

Tranylcypromine is used primarily for the treatment of major depressive disorder that has not responded to other antidepressants. It is also used off-label for the treatment of anxiety disorders, panic attacks, and obsessive-compulsive disorder.

It's important to note that MAOIs like tranylcypromine have several dietary and medication restrictions due to their potential to cause serious or life-threatening reactions when combined with certain foods or medications. Therefore, careful monitoring by a healthcare professional is necessary while taking this medication.

Haloperidol is an antipsychotic medication, which is primarily used to treat schizophrenia and symptoms of psychosis, such as delusions, hallucinations, paranoia, or disordered thought. It may also be used to manage Tourette's disorder, tics, agitation, aggression, and hyperactivity in children with developmental disorders.

Haloperidol works by blocking the action of dopamine, a neurotransmitter in the brain, which helps to regulate mood and behavior. It is available in various forms, including tablets, liquid, and injectable solutions. The medication can cause side effects such as drowsiness, restlessness, muscle stiffness, and uncontrolled movements. In rare cases, it may also lead to more serious neurological side effects.

As with any medication, haloperidol should be taken under the supervision of a healthcare provider, who will consider the individual's medical history, current medications, and other factors before prescribing it.

Analysis of Variance (ANOVA) is a statistical technique used to compare the means of two or more groups and determine whether there are any significant differences between them. It is a way to analyze the variance in a dataset to determine whether the variability between groups is greater than the variability within groups, which can indicate that the groups are significantly different from one another.

ANOVA is based on the concept of partitioning the total variance in a dataset into two components: variance due to differences between group means (also known as "between-group variance") and variance due to differences within each group (also known as "within-group variance"). By comparing these two sources of variance, ANOVA can help researchers determine whether any observed differences between groups are statistically significant, or whether they could have occurred by chance.

ANOVA is a widely used technique in many areas of research, including biology, psychology, engineering, and business. It is often used to compare the means of two or more experimental groups, such as a treatment group and a control group, to determine whether the treatment had a significant effect. ANOVA can also be used to compare the means of different populations or subgroups within a population, to identify any differences that may exist between them.

In the field of medicine, "time factors" refer to the duration of symptoms or time elapsed since the onset of a medical condition, which can have significant implications for diagnosis and treatment. Understanding time factors is crucial in determining the progression of a disease, evaluating the effectiveness of treatments, and making critical decisions regarding patient care.

For example, in stroke management, "time is brain," meaning that rapid intervention within a specific time frame (usually within 4.5 hours) is essential to administering tissue plasminogen activator (tPA), a clot-busting drug that can minimize brain damage and improve patient outcomes. Similarly, in trauma care, the "golden hour" concept emphasizes the importance of providing definitive care within the first 60 minutes after injury to increase survival rates and reduce morbidity.

Time factors also play a role in monitoring the progression of chronic conditions like diabetes or heart disease, where regular follow-ups and assessments help determine appropriate treatment adjustments and prevent complications. In infectious diseases, time factors are crucial for initiating antibiotic therapy and identifying potential outbreaks to control their spread.

Overall, "time factors" encompass the significance of recognizing and acting promptly in various medical scenarios to optimize patient outcomes and provide effective care.

Yawning is a reflex characterized by the involuntary opening of the mouth and deep inhalation of air, often followed by a long exhalation. While the exact purpose and mechanism of yawning are not fully understood, it's believed to be associated with regulating brain temperature, promoting arousal, or stretching the muscles of the jaw and face. Yawning is contagious in humans and can also be observed in various animal species. It usually occurs when an individual is tired, bored, or during transitions between sleep stages, but its underlying causes remain a subject of ongoing scientific research.

Mescaline is a naturally occurring psychoactive alkaloid that is found in several species of cacti, including the peyote (Lophophora williamsii), San Pedro (Echinopsis pachanoi), and Peruvian torch (Echinopsis peruviana) cacti. It is known for its ability to produce profound changes in consciousness, mood, and perception when ingested.

In a medical context, mescaline is classified as a hallucinogen or psychedelic drug. It works by binding to serotonin receptors in the brain, which leads to altered states of consciousness, including visual hallucinations, distorted perceptions of time and space, and altered emotional states.

It's important to note that while mescaline has been used for centuries in religious and spiritual practices among indigenous communities, its use is not without risks. High doses can lead to unpleasant or even dangerous psychological effects, such as anxiety, panic, and psychosis. Additionally, the legal status of mescaline varies by country and region, so it's important to be aware of local laws and regulations before using it.

3,4-Dihydroxyphenylacetic Acid (3,4-DOPAC) is a major metabolite of dopamine, which is a neurotransmitter in the brain. Dopamine is metabolized by the enzyme monoamine oxidase to form dihydroxyphenylacetaldehyde, which is then further metabolized to 3,4-DOPAC by the enzyme aldehyde dehydrogenase.

3,4-DOPAC is found in the urine and can be used as a marker for dopamine turnover in the brain. Changes in the levels of 3,4-DOPAC have been associated with various neurological disorders such as Parkinson's disease and schizophrenia. Additionally, 3,4-DOPAC has been shown to have antioxidant properties and may play a role in protecting against oxidative stress in the brain.

Prenylamine is not a medical term in and of itself, but it is the chemical name for a medication that is sometimes used in the medical field. The drug is known as Phenelzine sulfate in its brand name form, with trade names including Nardil.

Phenelzine sulfate (Prenylamine) is a type of medication called a monoamine oxidase inhibitor (MAOI). It works by blocking the action of an enzyme called monoamine oxidase, which helps break down certain chemicals in the brain called neurotransmitters. By blocking this enzyme's action, phenelzine sulfate increases the levels of these neurotransmitters in the brain, which can help to improve mood and alleviate symptoms of depression.

Phenelzine sulfate is used primarily to treat depression that has not responded to other treatments. It may also be used off-label for other conditions, such as anxiety disorders or panic attacks. However, it is important to note that phenelzine sulfate can have serious side effects and interactions with certain foods and medications, so it should only be taken under the close supervision of a healthcare provider.

Lisuride is a type of medication called a dopamine agonist, which works by stimulating dopamine receptors in the brain. It is primarily used to treat Parkinson's disease and related disorders, as it can help to alleviate symptoms such as stiffness, tremors, spasms, and poor muscle control.

Lisuride may also be used off-label for other conditions, such as certain types of headaches or cluster headaches. It is available in the form of tablets and is typically taken several times a day, with dosages adjusted based on individual patient needs and responses to treatment.

As with any medication, lisuride can have side effects, including nausea, dizziness, drowsiness, hallucinations, and orthostatic hypotension (low blood pressure upon standing). It is important for patients taking this medication to follow their healthcare provider's instructions carefully and report any unusual symptoms or concerns.

Norepinephrine plasma membrane transport proteins, also known as norepinephrine transporters (NET), are membrane-bound proteins that play a crucial role in the regulation of neurotransmission. They are responsible for the reuptake of norepinephrine from the synaptic cleft back into the presynaptic neuron, thereby terminating the signal transmission and preventing excessive stimulation of postsynaptic receptors.

The norepinephrine transporter is a member of the sodium-dependent neurotransmitter transporter family and functions as an antiporter, exchanging one intracellular sodium ion for two extracellular sodium ions along with the transport of norepinephrine. This sodium gradient provides the energy required for the active transport process.

Dysregulation of norepinephrine plasma membrane transport proteins has been implicated in various neurological and psychiatric disorders, such as attention deficit hyperactivity disorder (ADHD), depression, and post-traumatic stress disorder (PTSD). Therefore, understanding the function and regulation of these transporters is essential for developing novel therapeutic strategies to treat these conditions.

'Catha' is a plant species also known as Khat, Kat, or Qat. It contains psychoactive compounds that can cause stimulant-like effects when chewed, brewed into tea, or taken in other forms. The main active compound in Catha is cathinone, which is similar in structure and effects to amphetamines.

The use of Catha can produce feelings of euphoria, increased alertness, and talkativeness, but it can also cause side effects such as increased heart rate, blood pressure, and anxiety. Long-term use of Catha has been associated with a number of health problems, including tooth decay, gastrointestinal issues, and mental health disorders.

It's worth noting that the legal status of Catha varies by country and region. In some places, it is legal and widely used, while in others, it is considered a controlled substance and its use is restricted or prohibited.

The brain is the central organ of the nervous system, responsible for receiving and processing sensory information, regulating vital functions, and controlling behavior, movement, and cognition. It is divided into several distinct regions, each with specific functions:

1. Cerebrum: The largest part of the brain, responsible for higher cognitive functions such as thinking, learning, memory, language, and perception. It is divided into two hemispheres, each controlling the opposite side of the body.
2. Cerebellum: Located at the back of the brain, it is responsible for coordinating muscle movements, maintaining balance, and fine-tuning motor skills.
3. Brainstem: Connects the cerebrum and cerebellum to the spinal cord, controlling vital functions such as breathing, heart rate, and blood pressure. It also serves as a relay center for sensory information and motor commands between the brain and the rest of the body.
4. Diencephalon: A region that includes the thalamus (a major sensory relay station) and hypothalamus (regulates hormones, temperature, hunger, thirst, and sleep).
5. Limbic system: A group of structures involved in emotional processing, memory formation, and motivation, including the hippocampus, amygdala, and cingulate gyrus.

The brain is composed of billions of interconnected neurons that communicate through electrical and chemical signals. It is protected by the skull and surrounded by three layers of membranes called meninges, as well as cerebrospinal fluid that provides cushioning and nutrients.

Bread & Amphetamines (Khlyab i amfeti) (Bulgarian: "Хляб и амфети") is the fourth solo studio album by Bulgarian rapper Big Sha ...
The term "amphetamines" also refers to a chemical class, but, unlike the class of substituted amphetamines, the "amphetamines" ... ADZENYS XR-ODT (amphetamine extended-release orally disintegrating tablet) contains a 3 to 1 ratio of d- to l-amphetamine, a ... Following amphetamine uptake at VMAT2, amphetamine induces the collapse of the vesicular pH gradient, which results in the ... DYANAVEL XR contains d-amphetamine and l-amphetamine in a ratio of 3.2 to 1 ... The most common (≥2% in the DYANAVEL XR group ...
Look up amphetamine in Wiktionary, the free dictionary. Amphetamine is a stimulant drug. Amphetamine may also refer to: ... "Amphetamine", a song by Everclear from So Much for the Afterglow History and culture of amphetamines This disambiguation page ... amphetamine), the drug's levorotatory enantiomer Adderall, a brand of mixed amphetamine salts Lisdexamfetamine, a prodrug of ... Substituted amphetamine, a class of chemical compounds based upon the amphetamine structure Dextroamphetamine (dexamfetamine, ( ...
Amphetamine was first produced at the end of the 19th century. By the 1930s, amphetamine and some of its derivative compounds ... Substituted amphetamines are a class of compounds based upon the amphetamine structure; it includes all derivative compounds ... For example, (S)-amphetamine, commonly known as d-amphetamine or dextroamphetamine, displays five times greater psychostimulant ... Examples of substituted amphetamines are amphetamine (itself), methamphetamine, ephedrine, cathinone, phentermine, ...
Amphetamine (Chinese: 安非他命; Jyutping: on1 fei1 taa1 ming6) is a 2010 Hong Kong film starring Byron Pang and Thomas Price. It ... Byron Pang as Kafka Tom Price as Daniel Linda So as May Winnie Leung as Linda 安非他命_(電影) Amphetamine (film) An uncut version of ... 安非他命》雞姦戲變「黑畫面」准上映 [Amphetamine anal intercourse shots are changed to blackout for public screening]. Ming Pao (in Chinese). 1 ... The next morning, Daniel asks to do amphetamine with Kafka who maintains that despite all of his shortcomings, he
... refers to a state of psychological dependence on a drug in the amphetamine class. Stimulants such as ... Amphetamine use within teenagers can have lasting effects on their brain, in particular the prefrontal cortex. Amphetamine use ... When substituted amphetamines are used, drug tolerance develops rapidly. Amphetamine dependence has shown to have the highest ... this will combine the amphetamine with a negative thing or opposite stimulus. Treatment for amphetamines is growing at ...
"A Synthesis of Amphetamine. J. Chem. Educ. 51, 671 (1974)". Erowid.org. Retrieved 9 January 2011. Otto Snow (2002). Amphetamine ... Land Speed Record is an allusion to Hüsker Dü's amphetamine use.[citation needed] Amphetamine was widely abused in the 1980s ... Asia & Pacific Amphetamine-Type Stimulants Information Centre "Oliver Sacks: on amphetamines, Oliver Sacks Foundation". YouTube ... Other examples include the song "Amphetamine" by Alternative rock band Everclear, "Amphetamine" by Three Souls in My Mind, "20 ...
"Amphetamine Reptile Records Documentary The Color Of Noise". mxdwn.com. 13 October 2015. Retrieved 27 June 2020. "Amphetamine ... Amphetamine Reptile Records (or AmRep Industries) is a record label founded in 1986 by Tom Hazelmyer in Washington state. The ... "Protonic Reversal Ep169: Tom Hazelmyer (Amphetamine Reptile)". protonicreversal.com. 14 May 2020. Retrieved 27 June 2020. ... Amphetamine Reptile Tour - Friday, October 30, 1992, at The Ritz List of record labels Riemenschneider, Chris (October 3, 2005 ...
... amphetamine psychosis. Amphetamine, the parent compound of amphetamine-type stimulants was first synthesized by Romanian ... After its discovery, amphetamine was purified and put into medical use in the 1900s. Amphetamine was originally sold as a ... However, amphetamine-type stimulants is not prescribed for this use legally. Amphetamine is frequently used for pleasure and ... However, the urinary excretion of amphetamine and other ATS is highly dependent on the pH. A small amount of amphetamine is ...
Specific Amphetamine Reptile Records at Discogs (Discographies of American record labels, Amphetamine Reptile Records). ... Amphetamine Reptile Records is an American record label founded in 1986 by American musician Tom Hazelmyer. General " ... "Amphetamine Reptile Records Discography (1986-2000)". amphetaminereptile.com. Archived from the original on December 12, 2021. ...
Cocaine- and amphetamine-regulated transcript, also known as CART, is a neuropeptide protein that in humans is encoded by the ... Amphetamine Cocaine Douglass J, Daoud S (March 1996). "Characterization of the human cDNA and genomic DNA encoding CART: a ... cocaine-+and+amphetamine-regulated+transcript+protein at the U.S. National Library of Medicine Medical Subject Headings (MeSH ... Zhang M, Han L, Xu Y (November 2011). "Roles of cocaine- and amphetamine-regulated transcript in the central nervous system". ...
... (DOEF; also known as dimethoxyfluoroethylamphetamine) is a lesser-known psychedelic ... Substituted amphetamines, Fluoroethyl compounds, All stub articles, Psychoactive drug stubs). ...
"Amphetamines". AIC. Archived from the original on 2 April 2011. Retrieved 10 June 2011. "Hallucinogens". AIC. Archived from the ... Over two tonnes of precursor chemicals for the production of meth/amphetamines were detected at the Australian border in 2008- ... had used amphetamines in the past 12 months. According to the Australian Crime Commission, there is an increase in the number ... "the majority of amphetamines consumed in Australia is produced in this country in clandestine laboratories." Community impact ...
The CDSA was updated as a result of the Safe Streets Act changing amphetamines from Schedule 3 to Schedule 1; however, ... Methylone does not substitute for amphetamine or for the hallucinogenic DOM in animals trained to discriminate between these ... In New Zealand, although methylone is not explicitly scheduled and falls outside the strict definitions of an "amphetamine ... It is a member of the amphetamine, cathinone and methylenedioxyphenethylamine classes. Methylone is a slight modification of 3, ...
DYANAVEL XR contains d-amphetamine and l-amphetamine in a ratio of 3.2 to 1 ... The most common (≥2% in the DYANAVEL XR group ... The effects of amphetamine on the gastrointestinal tract are unpredictable. If intestinal activity is high, amphetamine may ... Amphetamine modulates the activity of most psychoactive drugs. In particular, amphetamine may decrease the effects of sedatives ... Amphetamine use disorders ... 3,788 (3,425-4,145) Greene SL, Kerr F, Braitberg G (October 2008). "Review article: amphetamines ...
ΔFosB is the most significant factor involved in both amphetamine addiction and amphetamine-induced sex addictions, which are ... Kraemer T, Maurer HH (August 1998). "Determination of amphetamine, methamphetamine and amphetamine-derived designer drugs or ... the metabolites of amphetamine. Among these metabolites, the active sympathomimetics are amphetamine, 4‑hydroxyamphetamine, 4‑ ... of 647 individuals with amphetamine dependence reporting six or more signs of amphetamine withdrawal listed in the DSM when the ...
Listed as a Schedule 1 as it is an analogue of amphetamine. The CDSA was updated as a result of the Safe Streets and ... Unlike many other substituted amphetamines, however, it is not primarily a stimulant. DOI has a stereocenter and R-(−)-DOI is ... 2,5-Dimethoxy-4-Substituted Amphetamines DOF DOB DOC "D101 DOI hydrochloride ≥98% (HPLC), solid". Retrieved 13 April 2008. ... "Controlled Drugs and Substances Act : Legislative history · Schedule I · Section 19: Tramadol [Proposed]; Amphetamines". ...
DYANAVEL XR contains d-amphetamine and l-amphetamine in a ratio of 3.2 to 1 ... The most common (≥2% in the DYANAVEL XR group ... In South Korea, amphetamines are prohibited. In Taiwan, amphetamines including Adderall are Schedule 2 drugs with a minimum ... The effects of amphetamine on the gastrointestinal tract are unpredictable. If intestinal activity is high, amphetamine may ... "Amphetamine". Drug Information Portal. U.S. National Library of Medicine. "Amphetamine sulfate". Drug Information Portal. U.S. ...
Rothman RB, Baumann MH, Dersch CM, Romero DV, Rice KC, Carroll FI, Partilla JS (January 2001). "Amphetamine-type central ... Amphetamines.com. 19 November 2002. Archived from the original on 27 February 2011. Retrieved 15 January 2011. Ryzik M (10 June ... such as ecstasy or amphetamines), as well as with heroin and benzodiazepines use, and can be considered as a bridge between the ... amphetamine, or heroin.[dubious - discuss] Crack cocaine looks like irregular shaped white rocks. Cocaine - a tropane alkaloid ...
ISBN 978-1-4786-1318-3. Goldberg, R (2009). "Cocaine amphetamines". Drugs Across the Spectrum. Brooks Cole. ISBN 978-0-495- ...
Gordon Alles Benzedrine Amphetamine Rasmussen, Nicolas, On speed : the many lives of amphetamine, New York University Press, ( ... Profetamine is the name of a generic form of amphetamine sulfate which was introduced in the 1940s. Apparently, it was a ...
"Captagon, ISIS's favorite amphetamine, explained". Vox. 20 November 2015. Retrieved 5 January 2017. Henley, Jon (13 January ... "WW II German soldiers, civilians dropped amphetamines to give them boost to battle allies". NY Daily News. Retrieved 5 January ... Rasmussen N (July 2006). "Making the first anti-depressant: amphetamine in American medicine, 1929-1950". J. Hist. Med. Allied ... Todd, Brian; McConnell, Dugald (21 November 2015). "Syria fighters may be fueled by amphetamines". CNN. Retrieved 22 November ...
95% of cannabis users also drank alcohol; 26% took amphetamines; 19% took ecstasy and only 2.7% reported not having used any ... This was found to be comparatively higher than hallucinogens (26%) and amphetamines (22%). Long-term cannabis users are at risk ...
β-PEA was also as effective as amphetamine in its ability to produce conditioned place preference (i.e., the process by which ... Administration of D-amphetamine and methylphenidate resulted in a markedly increased urinary excretion of PEA,20,60 suggesting ... Pharmacologic amphetamines, physiologic neuromodulators". Journal of Neurochemistry. 90 (2): 257-271. doi:10.1111/j.1471- ... Phenylethylamine (10), amphetamine [AMPH (11 & 12)], methylenedioxy methamphetamine [METH (13)] and N-methyl-4-phenylpyridinium ...
2-FA may be considered to be an analog of amphetamine, thus falling under the Federal Analog Act. As of October 2015 2-FA is a ... 2-Fluoroamphetamine (2-FA) is a stimulant drug from the amphetamine family which has been sold as a designer drug. 2- ... doi:10.1016/s0022-1139(02)00201-4. Costa E, Garattini S (1970). Amphetamines and Related Compounds. New York: Raven Press. p. ... Substituted amphetamines, Fluoroarenes, Designer drugs, Norepinephrine-dopamine releasing agents). ...
Pharmacologic amphetamines, physiologic neuromodulators". Journal of Neurochemistry. 90 (2): 257-271. doi:10.1111/j.1471- ... Freye, E. (2009). Pharmacology and abuse of cocaine, amphetamines, ecstasy and related designer drugs : a comprehensive review ...
The Royal Commissioner studied, examined and reported upon the following drugs - cannabis; narcotics; heroin; amphetamines, ...
I'd never had amphetamines. I was working for Brian Wilson at 3:30 AM when he wanted to have his amphetamines." It was also ... "had a fondness for amphetamines" at the time. Parks hesitantly confirmed this, but added, "Those were his amphetamines. They ... interview included an off-the-cuff comment by Brian Wilson saying that it was Parks who introduced him to LSD and amphetamines ...
... compared to amphetamine. Exceptions include 4-MTA, a para-substituted, non-neurotoxic amphetamine. The LD50 (mouse; i.p.) of 4- ... "4-Methyl-amphetamine: a health threat for recreational amphetamine users". Journal of Psychopharmacology. 27 (9): 817-822. doi: ... The subjective effects of 4-fluoroamphetamine include euphoria which some find similar to the effects of MDMA and amphetamine, ... Harvey JA (June 1978). "Neurotoxic action of halogenated amphetamines". Annals of the New York Academy of Sciences. 305 (1): ...
"Amphetamine". Pubchem. Retrieved 1 November 2020. "The Small Faces: Ian McLagan and Kenney Jones tell the story of their ... is a synonym for the central nervous system stimulant drug Amphetamine. However, in a 2014 interview with Uncut, McLagan stated ...
Bread & Amphetamines (Khlyab i amfeti) (Bulgarian: "Хляб и амфети") is the fourth solo studio album by Bulgarian rapper Big Sha ...
... including amphetamine, methamphetamine, dextroamphetamine, ephedrine, and others. Generally, these drugs generate emotional, ... Amphetamines are a class of central nervous system stimulants with a similar chemical structure, ... Amphetamines are a class of central nervous system stimulants with a similar chemical structure, including amphetamine, ... Amphetamine users may also use other drugs inappropriately to manage the side effects of amphetamines. Benzodiazepines, for ...
Amphetamine: learn about side effects, dosage, special precautions, and more on MedlinePlus ... Before taking amphetamine,. *tell your doctor and pharmacist if you are allergic to amphetamine, other stimulant medications ... If you or your child are taking amphetamine for ADHD, your doctor will probably start you on a low dose of amphetamine and ... Alcohol can make the side effects from amphetamine worse.. *you should know that amphetamine should be used as part of a total ...
An Experience with Amphetamines (Adderall). Ruined College by Amphuckedup ... "Ruined College: An Experience with Amphetamines (Adderall) (exp53643)". Erowid.org. Oct 30, 2008. erowid.org/exp/53643 ...
The brain damage caused by amphetamine use is still noticeable years later, say experts. ... Amphetamine users can become dependant on the drug, and withdrawal symptoms can cause depression and lethargy. Heavy, regular ... Amphetamines work by releasing large quantities of the brain stimulating chemical dopamine. Animal studies have shown brain ... The brain damage caused by amphetamine use is still noticeable years later, say experts. In fact, users undergo similar brain ...
... discusses the comparative efficacy and acceptability of psychosocial interventions for individuals with cocaine and amphetamine ... Clinical guidelines recommend psychosocial interventions for cocaine and amphetamine addiction as first-line treatment, but ... Psychosocial Interventions for Individuals With Cocaine and Amphetamine Addiction - Medscape - May 11, 2019. ... and long-term treatment of people with cocaine and/or amphetamine addiction.[1] ...
Amphetamines), read this information before you or your child start taking Adderall XR. Adderall is prescribed for the ... Generic ingredients: Amphetamines. Adderall Full Prescribing Information. Adderall Patient Information. Read the Medication ... Active Ingredients: dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, USP, ... amphetamine sulfate USP. Inactive Ingredients: gelatin capsules, hydroxypropylmethylcellulose, methacrylic acid copolymer, ...
Amphetamines (Adderall). Feeling on Point by Echo Morphine ... 1400 It sort of dawns on me that the amphetamine has taken ... I have years of experience with amphetamines but have just discovered beta-blockers. I love going out and driving, shopping on ... "Feeling on Point: An Experience with Propranolol & Amphetamines (Adderall) (exp97923)". Erowid.org. Sep 20, 2019. erowid.org/ ... Amphetamines (6), Pharms - Propranolol (72) : Various (28), Performance Enhancement (50), Combinations (3). ...
Synthetic amphetamine compounds commonly are produced in clandestine laboratories and vary in purity and potency. ... Amphetamines are a class of compounds increasingly abused in regions of the world such as the western United States, ... 16] Data from rural populations reveal that whites use amphetamines significantly more than blacks . [17] However, amphetamine ... Educate patients on the toxic effects of amphetamines and that amphetamines are not a safe alternative to cocaine use. For ...
... BOXED WARNING. AMPHETAMINES HAVE A HIGH POTENTIAL FOR ABUSE. ADMINISTRATION OF ... Amphetamine sulfate tablets can be taken with or without food.. *From time to time, your doctor may stop amphetamine sulfate ... Do not use amphetamine sulfate tablets for a condition for which it was not prescribed. Do not give amphetamine sulfate tablets ... Amphetamine Sulfate is a sympathomimetic amino of the amphetamine group. It is a white, odorless crystalline powder. It has a ...
What Are Amphetamines?. What Are Amphetamines?. Amphetamines (am-FET-eh-meenz) are very addictive stimulants. They speed up ... How Are Amphetamines Used?. Amphetamines are swallowed, smoked, snorted, or injected.. What Do Amphetamines Do?. No matter how ... What Else Are Amphetamines Called?. speed, uppers, dexies, bennies, hearts, truck drivers, black beauties, ice ... Even after users stop taking amphetamines, they may still have problems such as aggression, anxiety, and strong cravings for ...
... is a form of psychosis which can result from amphetamine or methamphetamine use. ... Amphetamine psychosis is a form of psychosis which can result from amphetamine or methamphetamine use. Typically it appears ... As amphetamine use increased after World War II, largely due to the widespread use of amphetamine compounds in nasal ... one of the four main characters clearly suffers from amphetamine psychosis after having been prescribed amphetamines as a ...
... * Sydney Morning Herald - UN warns on ... Shared Responsibility - United Nations Office on Drugs and Crime (UNODC) ranks amphetamine-type stimulants (ATS) such as ... The Irrawaddy News Magazine - Burma Pivotal as Amphetamine Use Soars (14 September 2011) ...
Find patient medical information for dextroamphetamine-amphetamine oral on WebMD including its uses, side effects and safety, ... Misuse or abuse of amphetamines may cause serious (possibly fatal) heart and blood pressure problems. Amphetamine-type ... Amphetamine/dextroamphetamine belongs to a class of drugs known as stimulants. It can help increase your ability to pay ... dextroamphetamine-amphetamine ER 5 mg 24hr capsule,extend release. Color: white,lime greenShape: oblongImprint: ELI-510 5 mg. ...
... of the dose is recoverable in urine as amphetamine itself. Since amphetamine has a pKa of 9 .9, urinary recovery of amphetamine ... 24 HR amphetamine 12.5 MG Extended Release Oral Tablet. SCD. 3. 1739803. amphetamine 12.5 MG 24 HR Extended Release ... 24 HR amphetamine 15.7 MG Extended Release Oral Tablet. SCD. 9. 1739813. amphetamine 15.7 MG 24 HR Extended Release ... 24 HR amphetamine 18.8 MG Extended Release Oral Tablet. SCD. 15. 1739819. amphetamine 18.8 MG 24 HR Extended Release ...
In both provocative and playful fashion, AMPHETAMINE depicts young men shooting amphetamines and making love in the era of sex ...
Drugs.com - Amphetamine. *Asia & Pacific Amphetamine - Type Stimulant Information Centre - a very extensive information source ... Template:PubChemLink (L-form - Levamphetamine or L-amphetamine). *Srisurapanont et al, Treatment for amphetamine dependence and ... Information and harm reduction strategies for amphetamines and other illicit drugs. *Amphetamines news page - Alcohol and Drugs ... Retrieved from "https://citizendium.org/wiki/index.php?title=Amphetamine/External_Links&oldid=369689" ...
Amphetamines. Sertraline safety. Sertraline dosage. Sertraline and sex. Sertraline and OCD. Alprazolam (Xanax). New ...
This topic contains 2 study abstracts on Amphetamine indicating it may contribute to Cardiomyopathy, Heart Failure, and ... Problem Substances : Acid Blockers, Alcohol Consumption, Amphetamine, Antibiotics, Chemotherapy, Heroin, Recombinant Bovine ... These drugs include cocaine, amphetamine, marijuana and heroin, and are generally not considered to have medicinal effects ... Pretreatment of mice with cannabidiol attenuated the amphetamine induced disruptive effects on prepulse inhibition (PPI).May 05 ...
Although clinical uses of amphetamines exist for adolescents, most notably for... ... Impact of Amphetamine Exposure During Adolescence on Neurobehavioral Endpoints. *Steven R. Boomhower. 3,4 ... Westbrook SR, Carrica LK, Banks A, Gulley JM (2020) AMPed-up adolescents: the role of age in the abuse of amphetamines and its ... Fletcher PJ, Tenn CC, Rizos Z, Lovic V, Kapur S (2005) Sensitization to amphetamine, but not PCP, impairs attentional set ...
The FDA had accepted for review Tris Pharmas New Drug Application for its extended-release liquid amphetamine to treat ADHD in ... Even though amphetamines are profoundly effective in treating ADHD, current formulations are less than ideal for pediatric ... FDA Accepts Liquid Amphetamine Application for ADHD. May 26, 2015. Krystle Vermes ... As an ER liquid amphetamine formulation with a great duration of action, Dyanavel XR has the potential to fulfill an important ...
Structure, properties, spectra, suppliers and links for: 4-Propoxy-2,5-dimethoxy amphetamine.
t:Amphetamine Annie} {st:Canned Heat} INTRO ****** {sot} e,--------------,--s ... Amphetamine Annie Canned Heat. e,--------------,--s-----------------,------------------------------,----------------------, B,- ...
... Curr ... Psychostimulants induce the strongest elevation in 50-kHz USV emission, particularly amphetamine (AMPH), either when applied ...
Amphetamine. Interview with director Scud. Scud Interview (Love Actually… Sucks!) Posted on June 25, 2011 by Le Anne Lindsay Q ...
Schmidt CJ Neurotoxicity of the psychedelic amphetamine, methylenedioxymethamphetamine J Pharmacol Exp Ther 1987 240(1):1-7 ... "Neurotoxicity of the psychedelic amphetamine, methylenedioxymethamphetamine" J Pharmacol Exp Ther. 1987;240(1):1-7. ...
... Why shouldnt the amphetamines be banned altogether, as in Sweden except, perhaps, for ... To evaluate the likelihood that amphetamine prohibition will work, let us examine in more detail the ways in which amphetamines ... 3 This is slightly less than the wholesale price of legally manufactured amphetamines 75 cents per thousand for five milligram ... It is the ideal solution to the speed problem and to the amphetamine problem in general. The only possible objection that can ...
Amphetamine will do the trick, but it will also cause your high achievers to slack off - at least if your employees are rats. ... Amphetamine Spurs Slackers to Work and Workers to Slack - at Least For Rats. New research underscores the value of studying ... Overall, amphetamine didnt affect accuracy.. High doses of caffeine, in contrast, reduced effort in workers, but had no effect ... Want to help your underperforming workers take on more challenging tasks? Amphetamine will do the trick, but it will also cause ...
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  • Amphetamines are a class of central nervous system stimulants with a similar chemical structure, including amphetamine , methamphetamine, dextroamphetamine, ephedrine, and others. (psychologytoday.com)
  • Of the amphetamines, methamphetamine likely has the largest potential for abuse. (psychologytoday.com)
  • Methamphetamine was developed early in the 20th century from its parent drug, amphetamine, and was used originally in nasal decongestants and bronchial inhalers. (psychologytoday.com)
  • For example, methamphetamine lacks much of the peripheral stimulant properties of amphetamine while still offering euphoric and hallucinogenic properties. (medscape.com)
  • Amphetamine psychosis is a form of psychosis which can result from amphetamine or methamphetamine use. (bionity.com)
  • three postmortem blood assays detected methamphetamine, and four qualitative screening tests detected amphetamine or amphetamine analogs in workers without amphetamine prescriptions. (cdc.gov)
  • According to the U.S. National Library of Medicine , use of amphetamine and methamphetamine is widespread in the general population and common among patients with psychiatric disorders. (amphetamines.com)
  • Amphetamine-related hospitalizations in our study were associated with socioeconomic characteristics and geographic patterns consistent with trends in methamphetamine use,' he said. (madinamerica.com)
  • The psychological effects of amphetamine addiction, and we see this especially with methamphetamine addicts, can be devastating and so the counseling and therapies are designed to reconstruct the thought process. (drug-addiction-support.org)
  • Amphetamines include the drug amphetamine and its many variants such as methamphetamine (speed or crystal meth) and methylenedioxymethamphetamine (MDMA, Ecstasy, or Adam). (msdmanuals.com)
  • Methamphetamine is the most commonly used amphetamine in the United States. (msdmanuals.com)
  • Amphetamine-type stimulants (ATS) such as "ecstasy" and methamphetamine now rank as Africa's second most widely abused drug type. (who.int)
  • Many amphetamines are Schedule II stimulants, which means they have a high potential for abuse and are legally available only through a prescription. (psychologytoday.com)
  • Amphetamine is in a class of medications called central nervous system stimulants. (medlineplus.gov)
  • Amphetamines (am-FET-eh-meenz) are very addictive stimulants. (akronchildrens.org)
  • Amphetamine / dextroamphetamine belongs to a class of drugs known as stimulants. (webmd.com)
  • Amphetamines are central nervous system stimulants that can induce hyperthermia independently or in combination with other risk factors ( 2 ). (cdc.gov)
  • A number of studies implicate prefrontal cortex function following repeated use of amphetamines (and other psychomotor stimulants) during the adolescent period. (springer.com)
  • A large body of evidence supports the hypothesis that mesolimbic dopamine (DA) mediates, in animal models, the reinforcing effects of central nervous system stimulants such as cocaine and amphetamine. (nih.gov)
  • The role DA plays in mediating amphetamine-type subjective effects of stimulants in humans remains to be established. (nih.gov)
  • If increases in NE mediate amphetamine-type subjective effects of stimulants in humans, then one would predict that stimulant medications that produce amphetamine-type subjective effects in humans should share the ability to increase NE. (nih.gov)
  • Importantly, the oral dose of these stimulants, which produce amphetamine-type subjective effects in humans, correlated with the their potency in releasing NE, not DA, and did not decrease plasma prolactin, an effect mediated by DA release. (nih.gov)
  • These results suggest that NE may contribute to the amphetamine-type subjective effects of stimulants in humans. (nih.gov)
  • Amphetamines are classified as stimulants and can be extremely addictive if not used as prescribed. (addictionblog.org)
  • Amphetamines are central nervous system (CNS) stimulants that are used to treat ADHD and narcolepsy. (meridianbioscience.com)
  • The quantitative and qualitative features of the behavioral response to amphetamine-like stimulants in rats can be dissociated from the dopamine response. (aspetjournals.org)
  • While most people are familiar with ADHD prescription stimulants such as Adderall or Ritalin, fewer patients are knowledgeable about Vyvanse, another prescription-only amphetamine. (teensavers.com)
  • Amphetamine-type stimulants : a global view. (who.int)
  • Amphetamines work by releasing large quantities of the brain stimulating chemical dopamine. (bbc.co.uk)
  • This is thought to be largely due to the increase in dopamine and perhaps serotonin activity in the mesolimbic pathway of the brain caused by amphetamine-like drugs, although other factors such as chronic sleep deprivation may also play a part. (bionity.com)
  • The link between amphetamine and psychosis is one of the major sources of evidence for the dopamine hypothesis of psychosis. (bionity.com)
  • During the adolescent period, monoamine neurotransmitter systems (particularly dopamine, norepinephrine, and serotonin) undergo continued development, and evidence from experimental animal models suggests that repeated use of amphetamines during this time can impact behavioral processes that rely on monoamine systems throughout the lifespan. (springer.com)
  • Further, evidence suggests that adolescent amphetamine exposure alters monoamine signaling and increases sensitivity to drugs that act on dopamine, norepinephrine, and serotonin later in life. (springer.com)
  • This dissociation is particularly evident in the temporal profiles of the extracellular dopamine and stereotypy responses to higher doses of amphetamine. (aspetjournals.org)
  • One possible mechanism contributing to this temporal dissociation is that during the acute response to amphetamine, dopamine receptor mechanisms are enhanced such that stereotyped behaviors can be supported by synaptic concentrations of dopamine which are not sufficient to initiate these behaviors. (aspetjournals.org)
  • To further explore the dynamics of stimulant sensitivity during the acute response, we examined the behavioral and extracellular dopamine responses to a low, nonstereotypy-producing dose of amphetamine (0.5 mg/kg) at various times after an acute, priming injection of 4.0 mg/kg when stereotypies had subsided and extracellular dopamine was approaching predrug baseline levels. (aspetjournals.org)
  • Our results suggest that an exposure to amphetamine results in a rapid sensitization of the stereotypy response which does not involve changes in the extracellular dopamine response but requires activation of dopamine receptors. (aspetjournals.org)
  • Amphetamines cause more dopamine to be released in the brain. (msdmanuals.com)
  • Amphetamines are non-catecholamine, sympathomimetic amines with CNS stimulant activity. (nih.gov)
  • Amphetamines, when compared to other stimulant type drugs, such as cocaine, are more probable at inducing psychosis in a user. (amphetamines.com)
  • Such a mechanism may be significantly implicated during binge patterns of stimulant abuse and may also play a role in the sensitization associated with repeated amphetamine administration. (aspetjournals.org)
  • Amphetamine powder is a white, odourless crystalline powder, which is an incredibly powerful central nervous system stimulant. (usnetads.com)
  • Amphetamines are stimulant drugs that are used to treat certain medical conditions but are also subject to abuse. (msdmanuals.com)
  • Methylenedioxymethamphetamine (MDMA) MDMA (3,4-methylenedioxymethamphetamine) is similar to an amphetamine but has both stimulant and hallucinogenic effects. (msdmanuals.com)
  • Amphetamine psychosis can include delusions , hallucinations and thought disorder . (bionity.com)
  • The link between amphetamine and psychosis was first made by Young and Scoville in 1938 1 and was originally considered to be a rare condition. (bionity.com)
  • One particular manifestation of psychosis associated with amphetamine use is delusional parasitosis or Ekbom's syndrome , where a person falsely believes themselves to be infested with parasites. (bionity.com)
  • Down and Out in Vegas, with Amphetamine Psychosis Again? (bionity.com)
  • In the film Requiem for a Dream , Sara Goldfarb, one of the four main characters clearly suffers from amphetamine psychosis after having been prescribed amphetamines as a weight loss drug, specifically, hallucinations of her refrigerator trying to devour her. (bionity.com)
  • The anti-drug advertising of the Montana Meth Project often focuses on the dangers of amphetamine psychosis. (bionity.com)
  • Connell, P.H. (1961) Amphetamine Psychosis . (bionity.com)
  • 3 Ellinwood, E.H, (1967) Amphetamine Psychosis. (bionity.com)
  • It uses material from the Wikipedia article "Amphetamine_psychosis" . (bionity.com)
  • If Bob were to use amphetamines heavily, could he get amphetamine psychosis? (hipforums.com)
  • The only reason I ask is that amphetamine psychosis is said to have the exact same symptoms as paranoid schizophrenia so if Bob were taking medicine to keep those symptoms from happening the medicine might make it so he can't have the symptoms of amphetamine psychosis. (hipforums.com)
  • One of the effects of amphetamine use -especially when taken in large doses- is amphetamine psychosis. (amphetamines.com)
  • Amphetamines may induce symptoms of psychosis very similar to those of acute schizophrenia spectrum psychosis. (amphetamines.com)
  • Amphetamine-induced psychosis can cause paranoia and related symptoms. (amphetamines.com)
  • A user experiencing paranoia due to amphetamine psychosis may think that someone is out to get them. (amphetamines.com)
  • The best way to avoid psychosis induced by amphetamine is not to use the drug, especially in large doses, and for long periods of time. (amphetamines.com)
  • Amphetamine abuse has negative side effects, among psychosis from a large dose, there is also the possibility of coma or death due to an overdose. (amphetamines.com)
  • The drug-induced sedation known as laxative psychosis buying Amphetamine online caused when the body's body's production of GABA the benzodiazepine GABAinhibitor drops and is reduced when you co-sleep. (guybarzilayartists.com)
  • Amphetamine, as the racemic form, differs from dextroamphetamine in a number of ways. (nih.gov)
  • Read the Medication Guide and, if available, the Patient Information Leaflet provided by your pharmacist before you start taking amphetamine / dextroamphetamine and each time you get a refill. (webmd.com)
  • It contains two drugs - dextroamphetamine and amphetamine. (usnodrugs.com)
  • Other potentials for amphetamine abuse include prescription medications often used for attention deficit disorder and various over-the-counter diet pills. (medscape.com)
  • Amphetamines can help increase focus and concentration and are often used to treat attention deficit disorder. (brewcrewball.com)
  • To identify additional cases of severe hyperthermia in which workers tested positive for amphetamines, and to support OSHA's enforcement activities, OOMN reviewed all medical records and investigation materials submitted by other OSHA offices to OOMN during January 1, 2010-August 31, 2019. (cdc.gov)
  • Third baseman Nick Delmonico -- one of the Brewers' top prospects -- has been suspended for 50 games after testing positive for amphetamines. (brewcrewball.com)
  • I have years of experience with amphetamines but have just discovered beta-blockers. (erowid.org)
  • The hyperthermia produced by amphetamines is similar to that of the serotonin syndrome. (medscape.com)
  • The present experiment was designed to examine this relationship for amphetamine analogs that varied in serotonin releasing potency and to evaluate whether serotonergic actions can affect reinforcing efficacy. (aspetjournals.org)
  • differs from other amphetamines in that it also interferes with the reuptake of serotonin (another neurotransmitter) in the brain. (msdmanuals.com)
  • No matter how a person takes amphetamines, these drugs hit with a fast high, making the user feel powerful, alert, and energized. (akronchildrens.org)
  • Even after users stop taking amphetamines, they may still have problems such as aggression, anxiety, and strong cravings for the drugs. (akronchildrens.org)
  • In both provocative and playful fashion, AMPHETAMINE depicts young men shooting amphetamines and making love in the era of sex, drugs and rock and roll. (lightcone.org)
  • Because many college students and executives attempt cognitive enhancement by using similar drugs non-medically, and the U.S. military actually prescribes amphetamines to pilots on some critical missions to combat the effects of sleep-deprivation. (time.com)
  • When a person abuses amphetamines their body develops a high tolerance for the drugs and creates a desire to use higher and more frequent doses. (addictionblog.org)
  • Certain drugs can cause false-positive results in urine drug screening for amphetamines including anti-depressants, anti-histamines, nasal inhalers and cold medicines that contain pseudoephedrine and/or promethazine. (meridianbioscience.com)
  • Amphetamine (Adderall) is one of the most concerning of all prescription drugs in the United States. (usnodrugs.com)
  • They are also known as co-sleeping because they can have some effects when you buying Amphetamine online with someone who is already on drugs. (guybarzilayartists.com)
  • Drugs that make you hyper focused buying Amphetamine make you believe you're doing something dangerous and dangerous things. (guybarzilayartists.com)
  • Drugs that can make you hyper buying Amphetamine may lead to feelings of buying Amphetamine or enjoyment which may lead to thoughts for drug use, taking drugs or sexual activity. (guybarzilayartists.com)
  • Some drugs trigger memories (releases of memory) in your brain which makes it buying Amphetamine to ignore and stay away from dangerous things. (guybarzilayartists.com)
  • Other drugs and substances may trigger certain buying Amphetamine of fear - for example anxiety. (guybarzilayartists.com)
  • Com is the largest online seller of online drugs and alcohol Amphetamine and may show the highest price. (guybarzilayartists.com)
  • The neuropeptide cocaine and amphetamine regulated transcript (CART) was shown to induce anxiety-like behavior in rodents, and mutations in the human CART gene are associated with depression and anxiety. (lu.se)
  • We show that neuronal populations expressing melanin-concentrating hormone (MCH) and cocaine and amphetamine-regulated transcript (CART) display a dose-dependent sensitivity to QA. (lu.se)
  • As amphetamine use increased after World War II, largely due to the widespread use of amphetamine compounds in nasal decongestant and dieting preparations, it became clear that chronic amphetamine use often led to psychotic symptoms. (bionity.com)
  • Hallucinations are frequently reported in chronic amphetamine users, with over 80% of users reporting the presence of hallucinatory experiences 2 , typically as visual or auditory experiences. (bionity.com)
  • Ersche KD, Roiser JP, Robbins TW, Sahakian BJ (2008) Chronic cocaine but not chronic amphetamine use is associated with perseverative responding in humans. (springer.com)
  • On low doses of amphetamine, the difference between the groups began to narrow, with slackers working harder and workers slacking off. (time.com)
  • High doses of amphetamines may raise body temperature to dangerous levels. (msdmanuals.com)
  • Boomhower SR, Newland MC (2019) d-Amphetamine and methylmercury exposure during adolescence alters sensitivity to monoamine uptake inhibitors in adult mice. (springer.com)
  • Buying Amphetamine online addictive substances that affect the central nervous system include benzodiazepines, such as Xanax and Klonopin. (guybarzilayartists.com)
  • 2 Kalant, O.J. (1966) The amphetamines: Toxicity and addiction Springfield, Ill: Charles C Thomas Publishers. (bionity.com)
  • As an ER liquid amphetamine formulation with a great duration of action, Dyanavel XR has the potential to fulfill an important unmet patient need. (pharmacytimes.com)
  • Psychostimulants induce the strongest elevation in 50-kHz USV emission, particularly amphetamine (AMPH), either when applied systemically or locally into the nucleus accumbens (Nacc). (nih.gov)
  • Amphetamine users can become dependant on the drug, and withdrawal symptoms can cause depression and lethargy. (bbc.co.uk)
  • Amphetamines use causes both immediate and long-term symptoms. (msdmanuals.com)
  • Clinical effects of amphetamine abuse are significant and commonly observed in emergency departments (EDs). (medscape.com)
  • Rather, we will focus on the abuse and addiction to amphetamines. (drug-addiction-support.org)
  • Even though Adderall is a brand name drug for amphetamine, it is also known by various other names among people who traffic, sell, and abuse it. (usnodrugs.com)
  • There is neither specific evidence which clearly establishes the mechanism whereby amphetamines produce mental and behavioral effects in children, nor conclusive evidence regarding how those effects relate to the condition of the central nervous system. (nih.gov)
  • Although clinical uses of amphetamines exist for adolescents, most notably for Attention-Deficit/Hyperactivity Disorder, the repeated recreational or illicit use of amphetamines during this time period has implications for long-term brain and behavioral development. (springer.com)
  • The number of hospitalizations that involved both opioids and amphetamines was six times higher in 2015 than in 2003. (madinamerica.com)
  • Your doctor will probably not prescribe amphetamine for you. (medlineplus.gov)
  • Also, is it O.K for a doctor to prescribe amphetamines to treat add for someone who also has schizophrenia? (hipforums.com)
  • Dr. Childress noted currently available capsule amphetamine formulations can be sprinkled or dissolved, but "patients may not ingest all of the product-or worse, may chew the sprinkles causing dose dumping. (pharmacytimes.com)
  • The larger the amount of the amphetamine dose taken, the more prone a user is to experience psychosi s . (amphetamines.com)
  • It is important to start with a low dose if you are new to taking Amphetamine, as the effects can be overwhelming. (guybarzilayartists.com)
  • The only possible objection that can be raised against banning amphetamines is that, like alcohol prohibition and heroin prohibition, it won't work. (druglibrary.net)
  • Then, the researchers introduced amphetamine, alcohol and caffeine into the equation. (time.com)
  • Amphetamine detoxification is not a dangerous procedure, unless the addict is also addicted to alcohol, in which case the withdrawal is potentially fatal and detoxification is an absolute must. (drug-addiction-support.org)
  • "Neurotoxicity of the psychedelic amphetamine, methylenedioxymethamphetamine" J Pharmacol Exp Ther . (erowid.org)
  • Dopaminergic (DA) and serotonergic (5-HT) projections to striatum and cortex have been implicated as the primary targets of substituted amphetamine (AMP)-induced neurotoxicity, largely on the basis of the propensity of these compounds to cause protracted decrements in DA and 5-HT rather than on the basis of AMP-induced alterations of indices linked to neural damage. (erowid.org)
  • Both amphetamine and cocaine increase norepinephrine (NE) via stimulation of release and inhibition of reuptake, respectively. (nih.gov)
  • The phenylethylamine structure of amphetamines (see the image below) is similar to catecholaminergic, dopaminergic, and serotonergic agonists (biogenic amines), which may explain their actions. (medscape.com)
  • Known hypersensitivity to amphetamine products or other ingredients in ADZENYS XR-ODT. (nih.gov)
  • however, while effects of cocaine last for 10-20 minutes, duration of amphetamine action is much longer-as long as 10-12 hours. (medscape.com)
  • This may be due to the duration of the effects of amphetamine on the brain. (amphetamines.com)
  • Amphetamines also inhibit monoamine oxidase, which degrades biogenic amine neurotransmitters intracellularly. (medscape.com)
  • Amphetamines are a class of compounds that are abused in many regions of the world, including the United States, Australasia, and Europe. (medscape.com)
  • Synthetic amphetamine compounds commonly are produced in clandestine laboratories and vary in purity and potency. (medscape.com)
  • Amphetamines are a group of structurally related compounds that produce central nervous system (CNS) and peripheral nervous system (PNS) stimulation. (medscape.com)
  • Amphetamine compounds cause a general efflux of biogenic amines from neuronal synaptic terminals (indirect sympathomimetics). (medscape.com)
  • Is the medical team experienced with amphetamine addiction treatment? (addictionblog.org)
  • There are thousands of rehab centers that currently provide amphetamine addiction treatment in the U.S. So, what's it like? (addictionblog.org)
  • Amphetamine addiction treatment begins with the addict admitting he/she is an addict. (drug-addiction-support.org)
  • Cognitive Behavior Therapy (CBT), 12 Step are solid options for amphetamine addiction treatment. (drug-addiction-support.org)
  • Amphetamine will do the trick, but it will also cause your high achievers to slack off - at least if your employees are rats. (time.com)
  • The current rat study found that both slacker and worker rats responded more impulsively on amphetamine. (time.com)
  • Amphetamine is detectable in blood for up to 48 hours, 5 days in urine and saliva, and up to three months in hair. (meridianbioscience.com)
  • Urine tests can detect most amphetamines. (msdmanuals.com)
  • Groups such as the Institute for the Study of Drug Dependence say that amphetamine use is actually falling, despite its association with the club scene. (bbc.co.uk)
  • The limited usefulness of amphetamines (see CLINICAL PHARMACOLOGY ) should be weighed against possible risks inherent in use of the drug, such as those described below. (nih.gov)
  • The FDA had accepted for review Tris Pharma's New Drug Application for its extended-release liquid amphetamine to treat ADHD in children. (pharmacytimes.com)
  • Therefore, amphetamine users have a higher possibility of developing a psychotic disorder with repeated use of the drug. (amphetamines.com)
  • Amphetamine is a prescription drug. (guybarzilayartists.com)
  • Because it is a powerful amphetamine-class drug, it is classified in the United States as a Schedule II controlled substance. (teensavers.com)
  • this may be important for understanding effects of amphetamine use on the fetus during pregnancy. (medscape.com)
  • Pretreatment of mice with cannabidiol attenuated the amphetamine induced disruptive effects on prepulse inhibition (PPI). (greenmedinfo.com)
  • Boomhower SR, Newland MC (2017) Effects of adolescent exposure to methylmercury and d-amphetamine on reversal learning and an extradimensional shift in male mice. (springer.com)
  • The effects of taking Amphetamine can last for a week to a month. (guybarzilayartists.com)
  • What are the side effects of Amphetamine in elderly? (guybarzilayartists.com)
  • Each tablet, for oral administration contains 5 mg or 10 mg of amphetamine sulfate. (nih.gov)
  • Research has found correlations between personality traits (risk taking and reward sensitivity) and responses to amphetamine use. (medscape.com)
  • Two cases involved legal use of prescription amphetamines to treat attention deficit hyperactivity disorder, and both persons who used legal prescription amphetamines died. (cdc.gov)
  • Gamma-linolenic acid for attention-deficit hyperactivity disorder: placebo-controlled comparison to D-amphetamine. (fabresearch.org)
  • In a Latin-square double-crossover with random assignment to sequence, 18 boys, aged 6-12 years, with attention-deficit hyperactivity disorder received 1 month each of placebo, D-amphetamine, and Efamol (evening primrose oil containing gamma-linolenic acid, with vitamin E as preservative). (fabresearch.org)
  • D- amphetamine is more effective at reducing hyperactivity and impulsiveness. (teensavers.com)
  • Your doctor or pharmacist will give you the manufacturer's patient information sheet (Medication Guide) when you begin treatment with amphetamine and each time you refill your prescription. (medlineplus.gov)
  • Clinical guidelines recommend psychosocial interventions for cocaine and amphetamine addiction as first-line treatment, but which of the many different interventions should be offered first? (medscape.com)
  • A team of investigators from the University of Oxford in England have performed a network meta-analysis to estimate the comparative effectiveness of all available psychosocial interventions (alone or in combination) for the short- and long-term treatment of people with cocaine and/or amphetamine addiction. (medscape.com)
  • Some recovering amphetamine users have found residential treatment programs the most beneficial because they are in a safe space, surrounded by peers and away from the temptations of social use. (addictionblog.org)
  • If you start buy Amphetamine experience suicidal tendencies, you buy Amphetamine seek treatment. (guybarzilayartists.com)
  • thus, the clinical presentation depends on the type of amphetamine used. (medscape.com)
  • Some amphetamines are not approved for medical use and are manufactured and used illegally. (msdmanuals.com)
  • This is a buy Amphetamine of prescription medication that reduces buy Amphetamine appetite. (guybarzilayartists.com)
  • Amphetamines suppress appetite and some people misuse amphetamines to lose weight. (msdmanuals.com)
  • L-amphetamine is better at improving concentration but may lead to increased anxiety. (teensavers.com)
  • Amphetamine (Evekeo, others) is also used to treat narcolepsy (a sleep disorder that causes excessive daytime sleepiness and sudden attacks of sleep). (medlineplus.gov)
  • Amphetamine (Evekeo, others) is also used for a limited period of time (a few weeks) along with a reduced calorie diet and an exercise plan for weight loss in obese people unable to lose weight. (medlineplus.gov)