Sitte Harald H, Freissmuth Michael
Institute of Pharmacology, Center for Physiology and Pharmacology, Medical University Vienna, Waehringerstrasse 13A, 1090 Vienna, Austria; Center for Addiction Research and Science (AddRess), Medical University Vienna, Waehringerstrasse 13A, 1090 Vienna, Austria.
Institute of Pharmacology, Center for Physiology and Pharmacology, Medical University Vienna, Waehringerstrasse 13A, 1090 Vienna, Austria.
Trends Pharmacol Sci. 2015 Jan;36(1):41-50. doi: 10.1016/j.tips.2014.11.006. Epub 2014 Dec 23.
In monoaminergic neurons, the vesicular transporters and the plasma membrane transporters operate in a relay. Amphetamine and its congeners target this relay to elicit their actions: most amphetamines are substrates, which pervert the relay to elicit efflux of monoamines into the synaptic cleft. However, some amphetamines act as transporter inhibitors. Both compound classes elicit profound psychostimulant effects, which render them liable to recreational abuse. Currently, a surge of new psychoactive substances occurs on a global scale. Chemists bypass drug bans by ingenuous structural variations, resulting in a rich pharmacology. A credible transport model must account for their distinct mode of action and link this to subtle differences in activity and undesired, potentially deleterious effects.
在单胺能神经元中,囊泡转运体和质膜转运体接力运作。苯丙胺及其同系物作用于这一接力过程以发挥其效应:大多数苯丙胺是底物,它们破坏这一接力过程,促使单胺外流至突触间隙。然而,一些苯丙胺充当转运体抑制剂。这两类化合物都会引发强烈的精神兴奋作用,使其易于被用于消遣性滥用。当前,全球范围内出现了大量新型精神活性物质。化学家通过巧妙的结构变化规避药物禁令,从而产生了丰富的药理学特性。一个可靠的转运模型必须解释它们独特的作用方式,并将其与活性的细微差异以及不良的潜在有害效应联系起来。