Mechanisms of neurotransmitter release by amphetamines: A review

被引:881
作者
Sulzer, D
Sonders, MS
Poulsen, NW
Galli, A
机构
[1] Columbia Univ, New York State Psychiat Inst, Dept Psychiat Neurol & Pharmacol, New York, NY 10032 USA
[2] Columbia Univ, Dept Pharmacol, New York, NY 10032 USA
[3] Columbia Univ, Ctr Mol Recognit, New York, NY 10032 USA
[4] Vanderbilt Univ, Ctr Mol Neurosci, Dept Physiol & Mol Biophys, Nashville, TN 37232 USA
关键词
D O I
10.1016/j.pneurobio.2005.04.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Amphetamine and substituted amphetamines, including methamphetamine, methylphenidate (Ritalin), methylenedioxymethamphetamine (ecstasy), and the herbs khat and ephedra, encompass the only widely administered class of drugs that predominantly release neurotransmitter, in this case principally catecholamines, by a non-exocytic mechanism. These drugs play important medicinal and social roles in many cultures, exert profound effects on mental function and behavior, and can produce neurodegeneration and addiction. Numerous questions remain regarding the unusual molecular mechanisms by which these compounds induce catecholamine release. We review current issues on the two apparent primary mechanisms - the redistribution of catecholamines from synaptic vesicles to the cytosol, and induction of reverse transport of transmitter through plasma membrane uptake carriers - and on additional drug effects that affect extracellular catecholamine levels, including uptake inhibition, effects on exocytosis, neurotransmitter synthesis, and metabolism. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:406 / 433
页数:28
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