Swift R M
Department of Psychiatry, Roger Williams Medical Center, Providence, RI 02908, USA.
J Clin Psychiatry. 1995;56 Suppl 7:24-9.
Opioid neurotransmitter systems have been shown to mediate certain aspects of alcohol consumption in animals and in humans. Use of opioid antagonists appears to decrease alcohol consumption in animals. Controlled clinical trials have indicated that alcohol-dependent subjects who are treated with a combination of naltrexone, an opioid antagonist, and traditional psychological and social therapies consume less alcohol and have lower relapse rates. The neurobiological mechanisms by which naltrexone acts to reduce alcohol consumption are still being investigated; however, there is evidence that naltrexone modifies the reinforcing effects of alcohol. Some researchers suggest that the reinforcing stimulant effects of alcohol and other psychoactive substances play a primary role in initiating and maintaining substance abuse and dependence. These effects may be mediated through the action of endogenous opioids. This article discusses the possible mechanisms of action of naltrexone and reviews human and animal studies that support the use of naltrexone in the treatment of alcohol dependence.
阿片类神经递质系统已被证明可介导动物和人类饮酒行为的某些方面。使用阿片类拮抗剂似乎会减少动物的酒精摄入量。对照临床试验表明,接受阿片类拮抗剂纳曲酮与传统心理和社会疗法联合治疗的酒精依赖者饮酒量减少,复发率降低。纳曲酮减少酒精摄入的神经生物学机制仍在研究中;然而,有证据表明纳曲酮会改变酒精的强化作用。一些研究人员认为,酒精和其他精神活性物质的强化刺激作用在引发和维持药物滥用及依赖方面起主要作用。这些作用可能通过内源性阿片类物质的作用来介导。本文讨论了纳曲酮可能的作用机制,并综述了支持纳曲酮用于治疗酒精依赖的人体和动物研究。