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Expert opinion on drug metabolism & toxicology • 2018 | View Paper
“An acute dose of (+)-amphetamine (15 mg/kg) decreased endogenous levels of DA and NE ; normal levels of DA were detected with chronic drug treatment and during withdrawal, with NE remaining slightly depressed.”
“Those in highest use are (1) methylphenidate and dextroamphetamine , which nonselectively block reuptake of both dopamine and norepinephrine ; and (2) L-dopa, the dopamine precursor, and bromocriptine, the dopamine (D2) receptor agonist.”
“ d-Amphetamine is markedly more potent an inhibitor of catecholamine uptake by norepinephrine neurons in the brain than is 1-amphetamine, whereas the two isomers are equally active in inhibiting catecholamine uptake by the dopamine neurons of the corpus striatum.”
“In addition to inhibiting the reuptake of DA and NA, d-amphetamine has also an effect in promoting the release of these neurotransmitters by being taken up into neuronal cells and then acting on the vesicular monoamine transporter.”
“ d-Amphetamine selectively promotes release of both dopamine (DA) and norepinephrine (NE) versus serotonin (5HT), and chronic d-amphetamine treatment decreases cocaine-taking behavior in rats, nonhuman primates, and humans.”
“First, after repeated d-amphetamine injections, a d-amphetamine challenge induces a dramatic increase in cortical extracellular norepinephrine ( NE ) levels.”