Yale School of Medicine, Department of Psychiatry, Yale University School of Medicine, Church St. South, Suite 109, New Haven, CT, 06519, USA.
Psychopharmacology (Berl). 2017 Sep;234(18):2737-2745. doi: 10.1007/s00213-017-4667-9. Epub 2017 Jun 9.
Clinical trials and human laboratory studies have established that varenicline can reduce rates of alcohol use among heavy drinkers. Less is known about the mechanisms by which varenicline has this effect on drinking behavior. Reactivity to alcohol cues is often cited as the primary cause of relapse among those being treated for alcohol use disorder, and several front-line treatments for alcohol use disorder work, at least in part, by minimizing cue-induced alcohol craving.
The current double-blind, placebo-controlled human laboratory study tested the effects of varenicline on alcohol cue reactivity in a group of heavy-drinking adult smokers and nonsmokers.
As part of a larger series of sequential human laboratory experiments testing the effects of varenicline on drinking outcomes, participants were assigned (between-participant) to receive either active varenicline (2 mg/day) or placebo. Following a titration period, participants (n = 77) attended a laboratory session during which they were exposed to alcohol and neutral cues using a standard cue reactivity paradigm.
Alcohol cue exposure increased craving for alcohol in both medication groups. However, participants receiving varenicline showed a smaller increase in alcohol craving compared to participants receiving placebo. The medication effect did not differ between smokers and nonsmokers. Among smokers, alcohol cue exposure also increased tobacco craving. Varenicline did not attenuate this effect.
Results support the use of varenicline for reducing alcohol use in heavy drinkers and identify a potential mechanism by which varenicline reduces drinking. Varenicline continues to show promise as a pharmacological treatment for alcohol use disorder.
临床试验和人体实验室研究已经证实,伐伦克林可降低重度饮酒者的饮酒率。关于伐伦克林对饮酒行为产生这种影响的机制知之甚少。对酒精线索的反应通常被认为是治疗酒精使用障碍患者复发的主要原因,而几种一线治疗酒精使用障碍的方法至少部分通过最小化线索诱导的酒精渴求起作用。
本项双盲、安慰剂对照的人体实验室研究旨在测试伐伦克林对一组重度饮酒的成年吸烟者和非吸烟者的酒精线索反应的影响。
作为一系列连续人体实验室实验的一部分,该实验测试了伐伦克林对饮酒结果的影响,参与者被(参与者间)分配接受伐伦克林(2 毫克/天)或安慰剂。在滴定期后,参与者(n=77)参加了一个实验室会议,在此期间,他们使用标准的线索反应范式暴露于酒精和中性线索。
酒精线索暴露增加了两组参与者对酒精的渴望。然而,与接受安慰剂的参与者相比,接受伐伦克林的参与者对酒精的渴望增加幅度较小。在吸烟者和非吸烟者中,药物的作用没有差异。在吸烟者中,酒精线索暴露也增加了对烟草的渴望。伐伦克林并没有减弱这种效果。
结果支持在重度饮酒者中使用伐伦克林来减少饮酒量,并确定了伐伦克林减少饮酒量的潜在机制。伐伦克林继续显示出作为治疗酒精使用障碍的药理学治疗方法的潜力。