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Erythroxylum coca
Erythroxylum coca

... m-opioid receptor KOs specifically lack responses to certain types of pain (next slide). 2. The a4b2 nicotinic receptor a4 or b2 nicotinic receptor knockouts: (1) respond less to nicotine in pain tests (next slide) (2) fail to self-administer nicotine (next slide). 3. The dopamine transporter Dopami ...
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... m-opioid receptor KOs specifically lack responses to certain types of pain (next slide). 2. The a4b2 nicotinic receptor a4 or b2 nicotinic receptor knockouts: (1) respond less to nicotine in pain tests (next slide) (2) fail to self-administer nicotine (next slide). 3. The dopamine transporter Dopami ...
Adverse effects
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... circulatory collapse. Headache, chills, and excessive sweating may also occur. Because of its cardiovascular effects, amphetamine should not be given to patients with cardiovascular disease or those receiving MAO inhibitors. Gastrointestinal system effects: anorexia, nausea, vomiting, abdominal cram ...
amphetamine sulphate
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... leading to a dental syndrome dubbed ‘meth mouth.’ Psychologically, regular and frequent speed use can cause a condition called Amphetamine Psychosis, typified by intense paranoia and anxiety. While the condition usually abates after the amphetamine use is discontinued, medical ...
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... Amphetamines are members of a class of drugs known as stimulants that includes caffeine, cocaine, and nicotine. Stimulants have the common property of increasing activity in the central nervous system (CNS). Some of these drugs are produced naturally by plants; others, like amphetamines, are the res ...
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Testing For Amphetamines And Related Compounds
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SE120144 - Sigma
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Amphetamines - EDAS Essential Drugs and Alcohol Services
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Essay B5 Chem 151 Professor Whitesell Amphetamines Honestly
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... treatment for attention deficit hyperactive disorder (ADHD). Adderall is a racemic mixture of dextroamphetamine and levoamphetamine (the D and L forms of the drug). Interestingly, it was found that dextroamphetamine form has a stronger effect on the CNS while the levoamphetamine form has a stronger ...
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fatovich_amphetamine.aspx
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... Professor Fatovich said there have been changing patterns of drug usage over time. In Australia the peak of heroin availability and use occurred around 1998–1999. This was followed by a shortage known as the “heroin drought” and a rise in amphetamine use, which peaked around 2005. This was followed ...
Slide 1
Slide 1

... The Controlled Substances Act of 1970 placed all drugs into one of five schedules. Restricted the manufacture, distribution and use of amphetamines. Limited the medically-accepted uses to narcolepsy, attention deficit disorders, and short-term obesity. Can only be received by a written prescripti ...
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Amphetamine



Amphetamine (contracted from alpha‑methylphenethylamine) is a potent central nervous system (CNS) stimulant that is used in the treatment of attention deficit hyperactivity disorder (ADHD), narcolepsy, and obesity. Amphetamine was discovered in 1887 and exists as two enantiomers: levoamphetamine and dextroamphetamine. Amphetamine properly refers to a specific chemical, the racemic free base, which is equal parts of the two enantiomers, levoamphetamine and dextroamphetamine, in their pure amine forms. However, the term is frequently used informally to refer to any combination of the enantiomers, or to either of them alone. Historically, it has been used to treat nasal congestion, depression, and obesity. Amphetamine is also used as a performance and cognitive enhancer, and recreationally as an aphrodisiac and euphoriant. It is a prescription medication in many countries, and unauthorized possession and distribution of amphetamine are often tightly controlled due to the significant health risks associated with recreational use.The first pharmaceutical amphetamine was Benzedrine, a brand of inhalers used to treat a variety of conditions. Currently, pharmaceutical amphetamine is prescribed as racemic amphetamine, Adderall, dextroamphetamine, or the inactive prodrug lisdexamfetamine. Amphetamine, through activation of a trace amine receptor, increases biogenic amine and excitatory neurotransmitter activity in the brain, with its most pronounced effects targeting the catecholamine neurotransmitters norepinephrine and dopamine. At therapeutic doses, this causes emotional and cognitive effects such as euphoria, change in libido, increased wakefulness, and improved cognitive control. It induces physical effects such as decreased reaction time, fatigue resistance, and increased muscle strength.Much larger doses of amphetamine may impair cognitive function and induce rapid muscle breakdown. Drug addiction is a serious risk with large recreational doses, but rarely arises from medical use. Very high doses can result in psychosis (e.g., delusions and paranoia) which rarely occurs at therapeutic doses even during long-term use. Recreational doses are generally much larger than prescribed therapeutic doses and carry a far greater risk of serious side effects.Amphetamine belongs to the phenethylamine class. It is also the parent compound of its own structural class, the substituted amphetamines, which includes prominent substances such as bupropion, cathinone, MDMA (ecstasy), and methamphetamine. As a member of the phenethylamine class, amphetamine is also chemically related to the naturally occurring trace amine neuromodulators, specifically phenethylamine and N-methylphenethylamine, both of which are produced within the human body. Phenethylamine is the parent compound of amphetamine, while N-methylphenethylamine is a constitutional isomer that differs only in the placement of the methyl group.
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