Opioid and cannabinoid systems as therapeutic targets for the treatment of alcohol dependence: From animal models to clinical practice

T. Femenía, Pablo Portillo, J. M. Pérez‐Ortiz, A. Aracil-Fernández, G. Rubio, J. Manzanares
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引用次数: 2

Abstract

The development of alcohol dependence is the result of a combination of various factors. Psychosocial and psychiatric conditions, together with functional alterations of the brain or genetic traits, contribute to the development of problems related to alcohol use or alcohol dependence. Clinical studies using neuroimaging techniques (PET, fMRI) and preclinical studies using different animal models of problems related to ethanol consumption have improved our knowledge of the neurochemical mechanisms involved in alcohol dependence. These studies have served to identify peptides or receptors modified by ethanol consumption, which are functionally altered in strains of rats or mice highly vulnerable to ethanol consumption. Such peptides or receptors may be interesting targets for the treatment of alcoholism. Among the different targets studied in recent years, the opioid and cannabinoid systems meet a number of conditions for eligibility as candidates for the treatment of alcohol dependence. The � -opioid receptor and cannabinoid CB1 receptor, in particular, are affected by ethanol consumption. In clinical studies, genetic polymorphisms of the � -opioid and CB1 receptors have been associated with increased vulnerability to alcohol consumption. Similarly, functional alterations in � - opioid and cannabinoid receptors have been identified in specific strains of rats or mice with high preference to ethanol consumption. Furthermore, several studies have shown that the manipulation of these receptors using agonists or antagonists may increase or decrease ethanol consumption, which confirms the validity of these receptors as targets for the treatment of alcohol dependence. In this review, we analyzed the genetic traits and psychiatric and/or psychosocial conditions that affect vulnerability to and the pharmacologic treatment of alcohol dependence, with special emphasis on the role of opioid and cannabinoid receptors. The use of animal models as important tools for identifying neurochemical mechanisms relevant to understanding and treating alcohol use problems was evaluated.
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阿片类药物和大麻素系统作为治疗酒精依赖的治疗靶点:从动物模型到临床实践
酒精依赖的发展是多种因素综合作用的结果。社会心理和精神状况,加上大脑功能或遗传特征的改变,导致出现与酒精使用或酒精依赖有关的问题。使用神经成像技术(PET, fMRI)的临床研究和使用不同动物模型的与乙醇消耗相关的问题的临床前研究提高了我们对涉及酒精依赖的神经化学机制的认识。这些研究用于鉴定乙醇消耗修饰的肽或受体,这些肽或受体在对乙醇消耗高度敏感的大鼠或小鼠品系中功能发生改变。这些多肽或受体可能是治疗酒精中毒的有趣靶点。在近年来研究的不同靶点中,阿片类药物和大麻素系统符合许多条件,可以作为治疗酒精依赖的候选者。特别是-阿片受体和大麻素CB1受体受到乙醇消耗的影响。在临床研究中,-阿片样物质和CB1受体的遗传多态性与饮酒易感性增加有关。类似地,在对乙醇消费有高度偏好的大鼠或小鼠的特定品系中,已经发现了-阿片样物质和大麻素受体的功能改变。此外,一些研究表明,使用激动剂或拮抗剂操纵这些受体可能会增加或减少乙醇消耗,这证实了这些受体作为治疗酒精依赖的靶点的有效性。在这篇综述中,我们分析了影响酒精依赖易感性和药物治疗的遗传特征、精神和/或社会心理状况,特别强调了阿片和大麻素受体的作用。使用动物模型作为识别与理解和治疗酒精使用问题相关的神经化学机制的重要工具进行了评估。
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