Rasmussen Dennis D, Kincaid Carrie L, Froehlich Janice C
VISN 20 Mental Illness Research, Education and Clinical Center, Seattle, Washington.
VA Puget Sound Health Care System, Seattle, Washington.
Alcohol Clin Exp Res. 2015 Sep;39(9):1832-41. doi: 10.1111/acer.12828. Epub 2015 Aug 11.
Prazosin (PRZ; an α1 -adrenergic receptor antagonist) and naltrexone (NTX; a nonspecific opioid receptor antagonist) each decrease alcohol drinking when administered to rats selectively bred for high voluntary alcohol drinking (alcohol-preferring or "P"), and the combination of PRZ + NTX decreases alcohol drinking more effectively than does either drug alone. As drug responsiveness can depend on history of alcohol drinking and dependence, we investigated whether various schedules of PRZ and NTX administration, alone or in combination, are effective in decreasing alcohol drinking in male P rats with a history of protracted voluntary alcohol drinking, dependence, and repeated withdrawals closely resembling human alcoholism.
Male P rats became alcohol-dependent during 1 year of ad libitum 24 h/d access to food, water, and 20% alcohol with repetitive temporary alcohol withdrawals. Four sequential studies then addressed effects of oral PRZ (2 mg/kg) and NTX (10 mg/kg), alone or together, on alcohol drinking during: (i) daily alcohol access with daily drug treatment, (ii) intermittent alcohol access with daily drug treatment, (iii) intermittent alcohol access with occasional drug treatment, and (iv) postdeprivation reinstatement of alcohol access.
The combination of PRZ + NTX consistently suppressed alcohol drinking during daily or intermittent alcohol access conditions and when drug treatment was either daily or occasional. PRZ + NTX was consistently more effective than either drug alone. The reduction in alcohol drinking was not due to sedation, motor effects, or malaise.
Both daily and "as-needed" treatment with PRZ + NTX are highly effective in suppressing daily, intermittent, and postdeprivation alcohol drinking in male P rats with a protracted history of alcohol dependence and repeated withdrawals. This drug combination may be especially effective for treating individuals with long histories of heavy alcohol abuse, dependence, and repeated relapse, as commonly encountered in clinical practice.
哌唑嗪(PRZ;一种α1 -肾上腺素能受体拮抗剂)和纳曲酮(NTX;一种非特异性阿片受体拮抗剂)在给予经选择性培育的高自愿饮酒(嗜酒或“P”型)大鼠时,各自都能减少酒精摄入,且PRZ + NTX联合用药比单独使用任一药物更有效地减少酒精摄入。由于药物反应性可能取决于饮酒和依赖史,我们研究了单独或联合使用PRZ和NTX的各种给药方案,对于有长期自愿饮酒、依赖和反复戒断史且与人类酒精中毒极为相似的雄性P大鼠减少酒精摄入是否有效。
雄性P大鼠在1年中每天24小时随意获取食物、水和20%酒精且经历重复性临时戒酒的过程中变得酒精依赖。随后的四项连续性研究探讨了口服PRZ(2毫克/千克)和NTX(10毫克/千克)单独或联合使用时,在以下情况下对酒精摄入的影响:(i)每日给予酒精并每日进行药物治疗,(ii)间歇性给予酒精并每日进行药物治疗,(iii)间歇性给予酒精并偶尔进行药物治疗,以及(iv)戒断后恢复酒精摄入。
在每日或间歇性给予酒精的情况下,以及药物治疗为每日或偶尔进行时,PRZ + NTX联合用药始终能抑制酒精摄入。PRZ + NTX始终比单独使用任一药物更有效。酒精摄入量的减少并非由于镇静、运动效应或不适。
对于有长期酒精依赖和反复戒断史的雄性P大鼠,每日和“按需”使用PRZ + NTX治疗在抑制每日饮酒、间歇性饮酒以及戒断后饮酒方面都非常有效。这种药物组合对于治疗临床实践中常见的有长期大量酗酒、依赖和反复复发史的个体可能特别有效。