Colombo Giancarlo, Serra Salvatore, Vacca Giovanni, Carai Mauro A M, Gessa Gian Luigi
C.N.R. Institute of Neuroscience, Viale Diaz, 182 I-09126 Cagliari (CA), Italy.
Pharmacol Biochem Behav. 2005 Jun;81(2):369-80. doi: 10.1016/j.pbb.2005.01.022.
The present paper describes the results of recent pharmacological studies implicating the cannabinoid CB1 receptor in the neural circuitry regulating alcohol consumption and motivation to consume alcohol. Cannabinoid CB1 receptor agonists have been found to specifically stimulate alcohol intake and alcohol's motivational properties in rats. Conversely, the cannabinoid CB1 receptor antagonist, SR 141716, has been reported to specifically suppress acquisition and maintenance of alcohol drinking behavior, relapse-like drinking and alcohol's motivational properties in rats. More recent data indicate that opioid receptor antagonists a) blocked the stimulatory effect of cannabinoids on alcohol intake, and b) synergistically potentiated the suppressing effect of SR 141716 on alcohol intake and alcohol's motivational properties. Consistently, SR 141716 blocked the stimulatory effect of morphine on alcohol intake. These results suggest a) the existence of a functional link between the cannabinoid and opioid receptor systems in the control of alcohol intake and motivation to consume alcohol, and b) that novel and potentially effective therapeutic strategies for alcoholism may come from the combination of cannabinoid and opioid receptor antagonists.
本文描述了近期药理学研究的结果,这些研究表明大麻素CB1受体参与调节酒精摄入和饮酒动机的神经回路。已发现大麻素CB1受体激动剂能特异性刺激大鼠的酒精摄入量及酒精的激发特性。相反,据报道大麻素CB1受体拮抗剂SR 141716能特异性抑制大鼠酒精饮用行为的习得和维持、类似复发的饮酒行为及酒精的激发特性。最新数据表明,阿片受体拮抗剂a)可阻断大麻素对酒精摄入的刺激作用,且b)能协同增强SR 141716对酒精摄入及酒精激发特性的抑制作用。同样,SR 141716也能阻断吗啡对酒精摄入的刺激作用。这些结果表明:a)在控制酒精摄入和饮酒动机方面,大麻素和阿片受体系统之间存在功能联系;b)针对酒精中毒的新型且可能有效的治疗策略可能源于大麻素和阿片受体拮抗剂的联合使用。