GABAergic mechanisms in alcohol dependence.

International review of neurobiology Pub Date : 2024-01-01 Epub Date: 2024-03-22 DOI:10.1016/bs.irn.2024.03.002
Mikko Uusi-Oukari, Esa R Korpi
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Abstract

The target of alcohol's effect on the central nervous system has been sought for more than 50 years in the brain's GABA system. The behavioral and emotional effects of alcohol in humans and rodents are very similar to those of barbiturates and benzodiazepines, and GABAA receptors have been shown to be one of the sites of alcohol action. The mechanisms of GABAergic inhibition have been a hotspot of research but have turned out to be complex and controversial. Genetics support the involvement of some GABAA receptor subunits in the development of alcohol dependence and in alcohol use disorders (AUD). Since the effect of alcohol on the GABAA system resembles that of a GABAergic positive modulator, it may be possible to develop GABAergic drug treatments that could substitute for alcohol. The adaptation mechanisms of the GABA system and the plasticity of the brain are a big challenge for drug development: the drugs that act on GABAA receptors developed so far also may cause adaptation and development of additional addiction. Human polymorphisms should be studied further to get insight about how they affect receptor function, expression or other factors to make reasonable predictions/hypotheses about what non-addictive interventions would help in alcohol dependence and AUD.

酒精依赖症中的 GABA 能机制。
50 多年来,人们一直在大脑的 GABA 系统中寻找酒精对中枢神经系统的作用靶点。酒精对人类和啮齿动物的行为和情绪影响与巴比妥类药物和苯二氮卓类药物非常相似,而 GABAA 受体已被证明是酒精作用的部位之一。GABA 能抑制的机制一直是研究的热点,但研究结果表明其机制复杂且存在争议。遗传学支持某些 GABAA 受体亚基参与酒精依赖和酒精使用障碍(AUD)的发展。由于酒精对 GABAA 系统的作用类似于 GABA 能正向调节剂,因此有可能开发出 GABA 能药物治疗方法来替代酒精。GABA 系统的适应机制和大脑的可塑性是药物开发的一大挑战:迄今为止开发的作用于 GABAA 受体的药物也可能会导致适应和产生额外的成瘾性。应进一步研究人类的多态性,以深入了解它们如何影响受体功能、表达或其他因素,从而合理预测/假设哪些非成瘾性干预措施有助于治疗酒精依赖和 AUD。
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