Spanagel R, Hölter S M
Max Planck Institute of Psychiatry, Munich, Federal Republic of Germany.
J Neural Transm (Vienna). 2000;107(6):669-80. doi: 10.1007/s007020070068.
A new animal model of alcoholism has been developed. Rats derived from this model show certain characteristics: (i) they have an incentive demand to consume alcohol, (ii) they exhibit relapse-like drinking even after a very long time of abstinence, (iii) they show tolerance to alcohol and have mild signs of physical withdrawal during the onset of abstinence, and (iv) during abstinence they also exhibit a psychological withdrawal syndrome consisting of enhanced anxiety-related behaviour and hyperreactivity to stressful situations. Anti-craving drugs such as acamprosate and naltrexone which proved to be effective in human alcoholics to prevent relapse were also effective in our animal model. Thus, both compounds suppressed the alcohol deprivation effect which is used as a measure for craving and relapse. It is concluded that this pharmacological validation of our model demonstrates the predictive value of our model and enables us to further characterize putative anti-craving drugs and neurobiological mechanisms of addictive behaviour.
一种新的酒精中毒动物模型已经建立。源自该模型的大鼠表现出某些特征:(i)它们有对酒精消费的动机需求;(ii)即使在很长时间戒酒之后,它们仍表现出复发性饮酒;(iii)它们对酒精产生耐受性,并在戒酒开始时出现轻微的身体戒断症状;(iv)在戒酒期间,它们还表现出一种心理戒断综合征,包括与焦虑相关行为的增强以及对应激情况的过度反应。在人类酒精中毒者中被证明对预防复发有效的抗渴望药物,如阿坎酸和纳曲酮,在我们的动物模型中也有效。因此,这两种化合物都抑制了用作渴望和复发指标的酒精剥夺效应。得出的结论是,我们模型的这种药理学验证证明了我们模型的预测价值,并使我们能够进一步表征假定的抗渴望药物和成瘾行为的神经生物学机制。