Hoffman P L, Tabakoff B
Department of Pharmacology, University of Colorado Health Sciences Center, Denver 80262, USA.
Alcohol Alcohol. 1996 Jul;31(4):333-40. doi: 10.1093/oxfordjournals.alcalc.a008159.
The alcohol dependence syndrome includes the presence of alcohol tolerance, physical dependence and an inability to control one's alcohol intake. Studies are reviewed that implicate the mesolimbic dopaminergic systems, and the gamma-aminobutyric acid-A (GABAA) and N-methyl-D-aspartate (NMDA) receptors as mediators of various aspects of the alcohol dependence syndrome. It is suggested that alcohol-induced changes in the GABAA receptor may play a role in certain aspects of tolerance to alcohol and in altered abilities of an individual to terminate alcohol intake. Chronic alcohol-induced increases in the activity of NMDA receptors may contribute to the withdrawal signs that are the defining feature of physical dependence on alcohol. It is hypothesized that decreased mesolimbic dopaminergic function, which occurs during alcohol withdrawal, may be involved in the compulsion to initiate and maintain alcohol drinking, another aspect of the alcohol dependence syndrome. Furthermore, evidence is presented that this decreased dopaminergic function could occur secondarily to the increase in NMDA receptor function, such that the alcohol-induced increase in NMDA receptor function could underlie both the overt withdrawal signs and the compulsion to drink alcohol in the alcohol-dependent individual.
酒精依赖综合征包括酒精耐受性、身体依赖性以及无法控制饮酒量。本文综述了一些研究,这些研究表明中脑边缘多巴胺能系统、γ-氨基丁酸A(GABAA)受体和N-甲基-D-天冬氨酸(NMDA)受体是酒精依赖综合征各个方面的介导因素。研究表明,酒精引起的GABAA受体变化可能在对酒精的某些耐受性方面以及个体终止饮酒能力的改变中起作用。慢性酒精引起的NMDA受体活性增加可能导致戒断症状,而戒断症状是身体对酒精依赖的决定性特征。据推测,在酒精戒断期间出现的中脑边缘多巴胺能功能降低,可能与开始和维持饮酒的冲动有关,这是酒精依赖综合征的另一个方面。此外,有证据表明,这种多巴胺能功能降低可能继发于NMDA受体功能的增加,因此酒精引起的NMDA受体功能增加可能是酒精依赖个体明显戒断症状和饮酒冲动的基础。