Endocannabinoid system and alcohol addiction: Pharmacological studies

被引:88
作者
Colombo, G
Serra, S
Vacca, G
Carai, MAM
Gessa, GL
机构
[1] CNR, Inst Neurosci, I-09126 Cagliari, CA, Italy
[2] Univ Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, Italy
关键词
cannabinoid CB1 receptor; WIN 55,212-2; CP 55,940; SR 141716 (rimonabant); opioid receptor; naloxone/naltrexone; alcohol intake; alcohol's motivational properties; sardinian alcohol-preferring (sP) rats;
D O I
10.1016/j.pbb.2005.01.022
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The present paper describes the results of recent pharmacological studies implicating the cannabinoid CB I receptor in the neural circuitry regulating alcohol consumption and motivation to consume alcohol. Cannabinoid CB, receptor agonists have been found to specifically stimulate alcohol intake and alcohol's motivational properties in rats. Conversely, the cannabinoid CB, 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. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:369 / 380
页数:12
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