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阿坎酸:对其在酒精依赖患者戒酒维持治疗中应用的综述

Acamprosate: a review of its use in the maintenance of abstinence in patients with alcohol dependence.

作者信息

Scott Lesley J, Figgitt David P, Keam Susan J, Waugh John

机构信息

Adis International Limited, Private Bag 65901, Mairangi Bay, Auckland, New Zealand.

出版信息

CNS Drugs. 2005;19(5):445-64. doi: 10.2165/00023210-200519050-00006.

Abstract

Acamprosate (Campral delayed-release tablet), a synthetic compound with a similar structure to that of the neurotransmitter GABA and the neuromodulator taurine, facilitates the maintenance of abstinence in detoxified alcohol-dependent patients. Although the precise mechanism(s) of action of the drug remains to be fully elucidated, it appears that it most likely involves beneficial modulation of the glutamatergic neurotransmitter system, including antagonism of the mGLu5 metabotropic glutamate receptor, to counteract the imbalance between the glutamatergic and GABAergic systems associated with chronic alcohol exposure and alcohol withdrawal. In several double-blind, placebo-controlled trials of up to 12 months' duration, acamprosate effectively maintained complete abstinence in detoxified alcohol-dependent patients, irrespective of disease severity or the type of psychosocial support. The drug showed better efficacy than placebo and was very well tolerated. Limited data from a relatively well designed trial indicate that the drug has similar efficacy to that of naltrexone and that combination therapy with these two agents provides better efficacy than acamprosate monotherapy, although multicentre direct head-to-head investigations are required to fully establish the potential of this combination. The drug may be particularly useful in those with hepatic impairment and/or liver disease. Thus, in combination with psychosocial and behavioural management programmes, acamprosate is a promising option for the maintenance of abstinence in alcohol-dependent patients after alcohol withdrawal.

摘要

阿坎酸(坎普拉尔缓释片)是一种结构与神经递质γ-氨基丁酸(GABA)及神经调质牛磺酸相似的合成化合物,可促进已戒酒的酒精依赖患者保持戒酒状态。尽管该药的确切作用机制仍有待充分阐明,但似乎很可能涉及对谷氨酸能神经递质系统的有益调节,包括对代谢型谷氨酸受体5(mGLu5)的拮抗作用,以抵消与长期酒精暴露及酒精戒断相关的谷氨酸能和GABA能系统之间的失衡。在多项长达12个月的双盲、安慰剂对照试验中,阿坎酸能有效维持已戒酒的酒精依赖患者完全戒酒,无论疾病严重程度或心理社会支持类型如何。该药疗效优于安慰剂,且耐受性良好。一项设计相对完善的试验提供的有限数据表明,该药与纳曲酮疗效相似,这两种药物联合治疗比阿坎酸单药治疗疗效更佳,不过需要多中心直接对比研究来全面确定这种联合用药的潜力。该药对肝功能损害和/或肝病患者可能特别有用。因此,与心理社会及行为管理方案相结合,阿坎酸是酒精依赖患者戒酒脱瘾后保持戒酒状态的一个有前景的选择。

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