Korpi E R
Biomedical Research Center, Alko Ltd, Helsinki, Finland.
Alcohol Alcohol. 1994 Mar;29(2):115-29.
Brain GABAergic mechanisms are interesting with regard to their role in the actions of ethanol. The present review summarizes some of the more recent studies, most of them biochemical, electrophysiological and pharmacogenetic. While there is still a number of controversies, e.g. regarding the molecular mechanisms of ethanol enhancement of GABAA receptor-mediated anion flux and the effects of chronic alcohol administration on the receptors in experimental animals and man, there is a substantial body of evidence supporting the involvement of these mechanisms in many behavioural actions of ethanol. Two recent findings warrant further molecular biological studies on the interaction between ethanol and the GABAA receptor, and the extension of the studies to human alcoholics: first, the effects of ethanol on the GABAA receptor are dependent on a specific gamma 2 subunit with an additional phosphorylation site; second, genetically enhanced sensitivity to the motor-impairing effect of moderate ethanol doses has a likely biological basis in a single-nucleotide mutation in a cerebellum-specific GABAA receptor subunit. Further studies are also needed to establish the role of GABAergic mechanisms in alcohol misuse and addiction.
就脑内γ-氨基丁酸(GABA)能机制在乙醇作用中的角色而言,它们很有意思。本综述总结了一些最新研究,其中大多数是生物化学、电生理学和药物遗传学方面的研究。尽管仍存在一些争议,例如关于乙醇增强GABAA受体介导的阴离子通量的分子机制以及慢性酒精给药对实验动物和人类受体的影响,但有大量证据支持这些机制参与了乙醇的许多行为作用。最近的两项发现值得对乙醇与GABAA受体之间的相互作用进行进一步的分子生物学研究,并将研究扩展至人类酗酒者:第一,乙醇对GABAA受体的影响取决于具有额外磷酸化位点的特定γ2亚基;第二,对中等剂量乙醇运动损害作用的遗传增强敏感性可能在小脑特异性GABAA受体亚基的单核苷酸突变中有生物学基础。还需要进一步研究以确定GABA能机制在酒精滥用和成瘾中的作用。