McColl S L, Burstein A H, Reeves K R, Billing C B, Stolar M, Sellers E M
Clinical Pharmacology, DecisionLine Clinical Research Corporation, Toronto, Ontario, Canada.
Clin Pharmacol Ther. 2008 Apr;83(4):607-14. doi: 10.1038/sj.clpt.6100510. Epub 2008 Feb 20.
Varenicline is an alpha(4)beta(2) nicotinic acetylcholine receptor partial agonist developed as an aid for smoking cessation. This study evaluated varenicline's potential for abuse by smokers (n = 23) and nonsmokers (n = 22). The study used a randomized, double-blind, placebo-controlled, double-dummy crossover design with five treatment periods: 15 and 30 mg amphetamine, 1 and 3 mg varenicline, and placebo. Following each treatment, the participants were assessed on aspects relating to potential abuse of the drug (e.g., drug liking, drug high, and drug monetary value). The positive effects measured for 3 mg varenicline were similar to those for the placebo, and significantly lower than those for amphetamine in both smokers and nonsmokers. Unpleasant effects were reported for 3 mg varenicline in both participant groups. For 1 mg varenicline, the overall patterns were similar, with the exception that the nonsmokers group showed some small positive effects balanced by some negative effects when compared with the effects of placebo. These findings lead to the conclusion that varenicline is unlikely to be abused.
伐尼克兰是一种开发用于辅助戒烟的α(4)β(2)烟碱型乙酰胆碱受体部分激动剂。本研究评估了伐尼克兰被吸烟者(n = 23)和非吸烟者(n = 22)滥用的可能性。该研究采用随机、双盲、安慰剂对照、双模拟交叉设计,有五个治疗阶段:15毫克和30毫克苯丙胺、1毫克和3毫克伐尼克兰以及安慰剂。每次治疗后,对参与者在与药物潜在滥用相关的方面进行评估(例如,对药物的喜好、药物兴奋感和药物货币价值)。在吸烟者和非吸烟者中,3毫克伐尼克兰所测得的积极效果与安慰剂相似,且显著低于苯丙胺的效果。两个参与者组均报告了3毫克伐尼克兰的不良影响。对于1毫克伐尼克兰,总体模式相似,不同之处在于与安慰剂的效果相比,非吸烟者组显示出一些小的积极效果,但也伴有一些消极效果。这些发现得出结论,伐尼克兰不太可能被滥用。