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5-羟色胺受体:对酒精及酒精中毒神经药理学的影响

5-HT receptors: implications for the neuropharmacology of alcohol and alcoholism.

作者信息

Overstreet D H, Rezvani A H, Pucilowski O, Janowsky D S

机构信息

Skipper Bowles Center for Alcohol Studies, University of North Carolina School of Medicine #7175, Chapel Hill 27599-7175, USA.

出版信息

Alcohol Alcohol Suppl. 1994;2:205-10.

PMID:8974337
Abstract

The involvement of serotonergic mechanisms in the neuropharmacology of alcohol was appreciated before it was recognized that there were multiple subtypes of serotonin (5-hydroxytryptamine; 5-HT) receptors. Thus, it was known that manipulations of the central serotonergic system could lead to a modification of the rate of tolerance development to alcohol (Frankel et al., 1975) or to a modulation of alcohol intake (Myers and Martin, 1973; Myers and Melchior, 1975) before Peroutka and Snyder (1979) first suggested that there were at least two subtypes of 5-HT receptors. Since these early reports were written, there has been a wealth of studies which have continued to support a role for 5-HT in the regulation of alcohol intake (See McBride et al., 1993b; Sellers et al., 1992, for reviews). Simultaneously, a tremendous expansion in the number of known 5-HT receptor subtypes has occurred (See Peroutka, 1988). However, there have not been, to our knowledge, any papers which have examined the possible role of specific 5-HT receptor subtypes in the regulation of alcohol's central effects. The present review addresses this deficiency in the literature. This review will focus on three major areas: the pharmacological regulation of alcohol intake; differences in 5-HT receptor subtypes among alcohol-preferring and -nonpreferring rat strains; and alterations in 5-HT receptor subtypes following chronic exposure to alcohol.

摘要

在人们认识到血清素(5-羟色胺;5-HT)受体存在多种亚型之前,就已经认识到血清素能机制参与了酒精的神经药理学作用。因此,在佩鲁特卡和斯奈德(1979年)首次提出至少存在两种5-HT受体亚型之前,人们就已经知道,对中枢血清素能系统的操作可导致对酒精耐受性发展速率的改变(弗兰克尔等人,1975年)或对酒精摄入量的调节(迈尔斯和马丁,1973年;迈尔斯和梅尔基奥尔,1975年)。自从撰写了这些早期报告以来,大量研究不断支持5-HT在调节酒精摄入量方面的作用(见麦克布赖德等人,1993b;塞勒斯等人,1992年的综述)。同时,已知的5-HT受体亚型数量也有了极大的增加(见佩鲁特卡,1988年)。然而,据我们所知,尚未有任何论文研究特定5-HT受体亚型在调节酒精中枢效应方面的可能作用。本综述旨在弥补文献中的这一不足。本综述将聚焦于三个主要领域:酒精摄入量的药理学调节;偏好酒精和不偏好酒精的大鼠品系之间5-HT受体亚型的差异;以及长期接触酒精后5-HT受体亚型的变化。

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引用本文的文献

1
Reduction in repeated ethanol-withdrawal-induced anxiety-like behavior by site-selective injections of 5-HT1A and 5-HT2C ligands.通过5-HT1A和5-HT2C配体的位点选择性注射减少重复乙醇戒断诱导的焦虑样行为。
Psychopharmacology (Berl). 2006 Jul;187(1):1-12. doi: 10.1007/s00213-006-0389-0. Epub 2006 May 19.
2
A 5-HT1A agonist and a 5-HT2c antagonist reduce social interaction deficit induced by multiple ethanol withdrawals in rats.一种5-羟色胺1A受体激动剂和一种5-羟色胺2c受体拮抗剂可减轻大鼠多次乙醇戒断所致的社交互动缺陷。
Psychopharmacology (Berl). 2003 Jun;167(4):344-52. doi: 10.1007/s00213-003-1425-y. Epub 2003 Apr 4.
3
Autoradiographic quantification of neurochemical markers of serotonin, dopamine and opioid systems in rat brain mesolimbic regions following chronic St John's wort treatment.
慢性圣约翰草治疗后大鼠脑海马边缘系统中血清素、多巴胺和阿片类系统神经化学标记物的放射自显影定量分析。
Naunyn Schmiedebergs Arch Pharmacol. 2003 Feb;367(2):126-33. doi: 10.1007/s00210-002-0666-3. Epub 2003 Jan 23.