Ernest Gallo Clinic and Research Center, University of California, San Francisco, 5858 Horton Street, Suite #200, Emeryville, CA 94608, USA.
Psychopharmacology (Berl). 2012 Oct;223(3):299-306. doi: 10.1007/s00213-012-2717-x. Epub 2012 May 1.
Emerging evidence suggests that the α4β2 form of the nicotinic acetylcholine receptor (nAChR) modulates the rewarding effects of alcohol. The nAChR α4β2 subunit partial agonist varenicline (Chantix™), which is approved by the Food and Drug Administration for smoking cessation, also decreases ethanol consumption in rodents (Steensland et al., Proc Natl Acad Sci U S A 104:12518-12523, 2007) and in human laboratory and open-label studies (Fucito et al., Psychopharmacology (Berl) 215:655-663, 2011; McKee et al., Biol Psychiatry 66:185-190 2009).
We present a randomized, double-blind, 16-week study in heavy-drinking smokers (n = 64 randomized to treatment) who were seeking treatment for their smoking. The study was designed to determine the effects of varenicline on alcohol craving and consumption. Outcome measures included number of alcoholic drinks per week, cigarettes per week, amount of alcohol craving per week, cumulative cigarettes and alcoholic drinks consumed during the treatment period, number of abstinent days, and weekly percentage of positive ethyl glucuronide and cotinine screens.
Varenicline significantly decreases alcohol consumption (χ (2) = 35.32, p < 0.0001) in smokers. Although varenicline has previously been associated with suicidality and depression, side effects were low in this study and declined over time in the varenicline treatment group.
Varenicline can produce a sustained decrease in alcohol consumption in individuals who also smoke. Further studies are warranted to assess varenicline efficacy in treatment-seeking alcohol abusers who do not smoke and to ascertain the relationship between varenicline effects on smoking and drinking.
新出现的证据表明,α4β2 型烟碱型乙酰胆碱受体(nAChR)调节酒精的奖赏效应。尼古丁乙酰胆碱受体 α4β2 亚单位部分激动剂伐仑克林(Chantix™)已获美国食品和药物管理局批准用于戒烟,也能减少啮齿动物(Steensland 等人,Proc Natl Acad Sci U S A 104:12518-12523,2007)和人类实验室及开放标签研究(Fucito 等人,Psychopharmacology(Berl)215:655-663,2011;McKee 等人,Biol Psychiatry 66:185-190,2009)中的乙醇消耗。
我们进行了一项随机、双盲、16 周的重度饮酒吸烟者(n=64 例随机接受治疗)研究,这些吸烟者正在寻求治疗以戒除吸烟。该研究旨在确定伐仑克林对酒精渴求度和饮酒量的影响。观察指标包括每周饮酒量、每周吸烟量、每周酒精渴求度、治疗期间累计饮酒量和吸烟量、无饮酒天数和每周乙基葡萄糖醛酸和可替宁检测阳性的百分比。
伐仑克林可显著减少吸烟者的饮酒量(χ(2)=35.32,p<0.0001)。尽管伐仑克林以前与自杀和抑郁有关,但本研究中的副作用较低,且随着时间的推移,在伐仑克林治疗组中逐渐减少。
伐仑克林可使同时吸烟的个体的饮酒量持续减少。需要进一步的研究来评估伐仑克林在不吸烟的寻求治疗的酒精滥用者中的疗效,并确定伐仑克林对吸烟和饮酒的影响之间的关系。