Verplaetse Terril L, Pittman Brian P, Shi Julia M, Tetrault Jeanette M, Coppola Sabrina, McKee Sherry A
Department of Psychiatry , Yale University School of Medicine, New Haven, Connecticut.
Department of Internal Medicine , Yale University School of Medicine, New Haven, Connecticut.
Alcohol Clin Exp Res. 2016 Jul;40(7):1567-76. doi: 10.1111/acer.13110. Epub 2016 Jun 1.
Varenicline has been found to decrease alcohol-motivated behaviors. Recent warnings regarding aversive events associated with varenicline used in conjunction with alcohol warrant further investigation into the safety of the drug when combined with alcohol. The purpose of this preliminary investigation was to examine the effect of combining varenicline with a high, fixed dose of alcohol on subjective reactivity and cognitive function in adults with alcohol use disorders (AUDs).
This double-blind, placebo-controlled preliminary investigation examined the effects of varenicline (0, 1, 2 mg/d) on subjective reactivity, cognition, perceptual motor function, and physiologic reactivity to a fixed dose of alcohol (vs. nonalcohol control beverage) using an established laboratory paradigm in smokers and nonsmokers meeting criteria for AUDs (n = 44). All participants had completed a parent varenicline study evaluating alcohol self-administration. Each subject completed 2 fixed-dose laboratory sessions assessing reactivity to a high-dose alcohol (0.08 g/dl) or a nonalcoholic control beverage, order counterbalanced.
Varenicline attenuated alcohol-related increases in subjective intoxication and alcohol-related decreases in executive cognitive function. At baseline, varenicline reduced alcohol craving and diastolic blood pressure, and increased associative learning, working memory, and perceptual motor function. Varenicline produced nonspecific effects on diastolic blood pressure and heart rate. Overall, there were few differences in effects between 1 and 2 mg/d varenicline versus placebo.
These preliminary results continue to support the safety and use of varenicline in combination with alcohol in individuals meeting criteria for AUDs.
已发现伐尼克兰可减少与酒精相关的行为。近期有关伐尼克兰与酒精联合使用时出现不良事件的警告,使得有必要进一步研究该药物与酒精联合使用时的安全性。这项初步研究的目的是检验伐尼克兰与高剂量、固定剂量酒精联合使用对患有酒精使用障碍(AUD)的成年人主观反应性和认知功能的影响。
这项双盲、安慰剂对照的初步研究,使用既定的实验室范式,在符合AUD标准的吸烟者和非吸烟者中(n = 44),检验伐尼克兰(0、1、2毫克/天)对主观反应性、认知、感知运动功能以及对固定剂量酒精(与非酒精对照饮料相比)的生理反应性的影响。所有参与者都完成了一项评估酒精自我给药的伐尼克兰母体研究。每个受试者完成2次固定剂量实验室测试,评估对高剂量酒精(0.08克/分升)或非酒精对照饮料的反应性,测试顺序采用平衡法。
伐尼克兰减弱了与酒精相关的主观醉酒增加以及与酒精相关的执行认知功能下降。在基线时,伐尼克兰减少了对酒精的渴望和舒张压,并增强了联想学习、工作记忆和感知运动功能。伐尼克兰对舒张压和心率产生了非特异性影响。总体而言,1毫克/天和2毫克/天的伐尼克兰与安慰剂之间在效果上几乎没有差异。
这些初步结果继续支持伐尼克兰在符合AUD标准的个体中与酒精联合使用的安全性和有效性。