Krystal John H, Staley Julie, Mason Graeme, Petrakis Ismene L, Kaufman Joan, Harris R Adron, Gelernter Joel, Lappalainen Jaakko
Department of Psychiatry, Division of Human Genetics, Yale University School of Medicine, 950 Campbell Avenue, New Haven, CT 06516, USA.
Arch Gen Psychiatry. 2006 Sep;63(9):957-68. doi: 10.1001/archpsyc.63.9.957.
Alcohol facilitates gamma-aminobutyric acid (GABA) function, and GABA type A (GABA(A)) receptor-facilitating agents suppress alcohol withdrawal symptoms. Advances in molecular neuroscience, genetics, and neuroimaging provide new insights into the role of brain GABA systems in short- and long-term alcohol effects.
To review the role of brain GABA systems in alcohol response, alcohol dependence, alcoholism vulnerability, and alcoholism pharmacotherapy.
Literature review.
Alcohol increases GABA release, raises neurosteroid levels, and may potently enhance the function of a GABA(A) receptor subclass that shows high affinity for GABA and neurosteroids, relative insensitivity to benzodiazepines, low chloride conductance, and an extrasynaptic location. Variation in GABA(A) receptor subunit genes may contribute to the vulnerability to alcoholism, particularly in the context of environmental risk factors. Alcohol dependence is associated with time-dependent changes in brain GABA(A) receptor density and subunit gene expression levels that contribute to a withdrawal-related deficit in GABA(A) receptor function. However, cortical GABA levels are not reduced during acute withdrawal. Benzodiazepine-assisted detoxification enhances a phasic component of GABA function. However, novel treatments target the tonic component of GABA neurotransmission mediated by benzodiazepine-insensitive GABA(A) receptors. Smoking attenuates withdrawal-related disturbances in brain GABA function, perhaps contributing to comorbid nicotine and alcohol dependence. The GABA systems show recovery with long-term sobriety.
Recent research deepens our understanding of the role of GABA systems in alcohol action, alcohol dependence, and the vulnerability to alcoholism. Also, GABA(A) receptor subtype-selective treatments merit exploration for reducing withdrawal symptoms and drinking in alcohol-dependent individuals.
酒精可促进γ-氨基丁酸(GABA)功能,且GABA A型(GABA(A))受体促进剂可抑制酒精戒断症状。分子神经科学、遗传学和神经影像学的进展为脑GABA系统在酒精短期和长期效应中的作用提供了新的见解。
综述脑GABA系统在酒精反应、酒精依赖、酒精成瘾易感性及酒精成瘾药物治疗中的作用。
文献综述。
酒精可增加GABA释放、提高神经甾体水平,并可能显著增强一类对GABA和神经甾体具有高亲和力、对苯二氮䓬相对不敏感、氯离子传导率低且位于突触外的GABA(A)受体亚类的功能。GABA(A)受体亚基基因的变异可能导致酒精成瘾易感性增加,尤其是在存在环境危险因素的情况下。酒精依赖与脑GABA(A)受体密度和亚基基因表达水平的时间依赖性变化有关,这些变化导致了GABA(A)受体功能的戒断相关缺陷。然而,急性戒断期间皮质GABA水平并未降低。苯二氮䓬辅助脱毒可增强GABA功能的一个时相成分。然而,新的治疗方法针对的是由对苯二氮䓬不敏感的GABA(A)受体介导的GABA神经传递的紧张性成分。吸烟可减轻脑GABA功能的戒断相关紊乱,这可能导致尼古丁和酒精依赖共病。GABA系统在长期戒酒时会恢复。
最近的研究加深了我们对GABA系统在酒精作用、酒精依赖和酒精成瘾易感性中的作用的理解。此外,GABA(A)受体亚型选择性治疗在减少酒精依赖个体的戒断症状和饮酒方面值得探索。