Laboratory of Clinical and Translational Studies, National Institute on Alcohol Abuse and Alcoholism, 10 Center Drive, 10 CRC-Hatfield Center, Rm. 1-5330, MSC 1108, Bethesda, MD 20892-1108, USA.
Psychopharmacology (Berl). 2010 Jan;208(1):37-44. doi: 10.1007/s00213-009-1704-3. Epub 2009 Nov 10.
There is an extensive literature showing that the CB(1) cannabinoid receptor antagonist rimonabant (SR141716) decreases alcohol consumption in animals, but little is known about its effects in human alcohol drinkers.
In this study, 49 nontreatment-seeking heavy alcohol drinkers participated in a 3-week study. After a 1-week baseline, participants received either 20 mg/day of rimonabant or placebo for 2 weeks under double-blind conditions. During these 3 weeks, participants reported their daily alcohol consumption by telephone. Subsequently, they participated in an alcohol self-administration paradigm in which they received a priming dose of alcohol followed by the option of consuming either eight alcohol drinks or receiving $3.00 for each nonconsumed drink. Endocrine measures and self-rating scales were also obtained.
Rimonabant did not change alcohol consumption during the 2 weeks of daily call-ins. Similarly, the drug did not change either alcohol self-administration or endocrine measures during the laboratory session.
We conclude that the daily administration of 20 mg of rimonabant for 2 weeks has no effect on alcohol consumption in nontreatment-seeking heavy alcohol drinkers.
有大量文献表明,CB(1) cannabinoid 受体拮抗剂利莫那班(SR141716)可减少动物的酒精摄入量,但对于其在人类酒精饮用者中的作用知之甚少。
在这项研究中,49 名非治疗性寻求的重度酒精饮用者参加了为期 3 周的研究。在基线期的 1 周后,参与者在双盲条件下接受 20 毫克/天的利莫那班或安慰剂治疗 2 周。在这 3 周内,参与者通过电话报告他们的每日饮酒量。随后,他们参加了酒精自我给药范式,其中他们接受了酒精的启动剂量,然后可以选择饮用 8 杯酒,或者每不饮酒可获得 3.00 美元。还获得了内分泌测量和自我评估量表。
利莫那班在每日电话随访的 2 周内并未改变酒精摄入量。同样,该药物在实验室期间也没有改变酒精自我给药或内分泌测量。
我们的结论是,每天给予 20 毫克利莫那班 2 周对非治疗性重度酒精饮用者的饮酒量没有影响。