Trace Amines and Their Relevance to Psychiatry and Neurology: A Brief Overview

Q Medicine
Deepak Narang, Sara E. Tomlinson, A. Holt, D. Mousseau, G. Baker
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引用次数: 18

Abstract

The arylalkylamines, s-phenylethylamine, m- and p-tyramine, tryptamine, m- and p-octopamine, phenylethanolamine and synephrine, have been termed trace amines because of their low absolute concentrations in the central nervous system relative to the classical neurotransmitter amines, noradrenaline, dopamine and 5-hydroxytryptamine (5-HT, serotonin). Despite being present at low concentrations, these amines have been implicated in the etiology and pharmacotherapy of several psychiatric and neurological disorders. Studies on trace amines þourished in the 1970s and 1980s, following the development of sensitive assays for these amines, and were accompanied by comprehensive electrophysiological studies and some receptor binding studies. There has been a resurgence of interest in these amines in the past decade with the discovery and cloning of a unique family of G-protein-coupled receptors, some of which are selectively activated by trace amines; these receptors have been termed trace amine, associated receptors (TAARs). The relevance of these receptors to the actions of the trace amines and to the actions of several other neurochemicals and psychotropic drugs is discussed.
微量胺及其与精神病学和神经病学的相关性:简要概述
芳基烷基胺、s-苯基乙胺、间和对酪胺、色胺、间和对章鱼胺、苯乙醇胺和辛弗林被称为微量胺,因为它们在中枢神经系统中的绝对浓度低于经典的神经递质胺、去甲肾上腺素、多巴胺和5-羟色胺(5-HT、5-羟色胺)。尽管这些胺的浓度很低,但它们与几种精神和神经疾病的病因学和药物治疗有关。随着对微量胺的灵敏测定方法的发展,对微量胺的研究在20世纪70年代和80年代开始兴起,并伴随着全面的电生理研究和一些受体结合研究。在过去的十年中,随着g蛋白偶联受体的独特家族的发现和克隆,对这些胺的兴趣重新燃起,其中一些受体被微量胺选择性激活;这些受体被称为微量胺相关受体(TAARs)。讨论了这些受体与微量胺的作用以及其他几种神经化学物质和精神药物的作用的相关性。
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来源期刊
CiteScore
0.34
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
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