Farokhnia M, Schwandt M L, Lee M R, Bollinger J W, Farinelli L A, Amodio J P, Sewell L, Lionetti T A, Spero D E, Leggio L
Section on Clinical Psychoneuroendocrinology and Neuropsychopharmacology, National Institute on Alcohol Abuse and Alcoholism and National Institute on Drug Abuse, National Institutes of Health, Bethesda, MD, USA.
Office of the Clinical Director, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA.
Transl Psychiatry. 2017 Apr 25;7(4):e1108. doi: 10.1038/tp.2017.71.
Baclofen has been suggested as a potential pharmacotherapy for alcohol use disorder, but the clinical data are conflicting. Here we investigated the biobehavioral effects of baclofen in a sample of anxious alcohol-dependent individuals. This was a randomized, double-blind, placebo-controlled, human laboratory study in non-treatment seeking alcohol-dependent individuals with high trait anxiety (N=34). Participants received baclofen (30 mg per day) or placebo for at least 8 days, then performed an experimental session consisting of alcohol cue-reactivity followed by alcohol administration procedure (alcohol priming, then alcohol self-administration). Total amount of alcohol self-administered was the primary outcome; alcohol craving, subjective/physiological responses and mood/anxiety symptoms were also evaluated. There was no significant medication effect on the total amount of alcohol consumed during the alcohol self-administration (P=0.76). Baclofen blunted the positive association between maximum breath alcohol concentration during priming and the amount of alcohol consumption (significant interaction, P=0.03). Ratings of feeling intoxicated were significantly higher in the baclofen group after consuming the priming drink (P=0.006). During the self-administration session, baclofen significantly increased ratings of feeling high (P=0.01) and intoxicated (P=0.01). A significant reduction in heart rate (P<0.001) and a trend-level increase in diastolic blood pressure (P=0.06) were also detected in the baclofen group during the alcohol laboratory session. In conclusion, baclofen was shown to affect subjective and physiological responses to alcohol drinking in anxious alcohol-dependent individuals. These results do not support an anti-craving or anti-reinforcing effect of baclofen, but rather suggest that baclofen may act as a substitution medication for alcohol use disorder.
巴氯芬已被提议作为酒精使用障碍的一种潜在药物疗法,但临床数据相互矛盾。在此,我们调查了巴氯芬对焦虑型酒精依赖个体样本的生物行为影响。这是一项针对特质焦虑水平高的未寻求治疗的酒精依赖个体的随机、双盲、安慰剂对照人体实验室研究(N = 34)。参与者接受巴氯芬(每日30毫克)或安慰剂治疗至少8天,然后进行一个实验环节,包括酒精线索反应性测试,随后是酒精给药程序(酒精激发,然后酒精自我给药)。酒精自我给药的总量是主要结果;还评估了酒精渴望、主观/生理反应以及情绪/焦虑症状。在酒精自我给药期间,药物对酒精消耗量没有显著影响(P = 0.76)。巴氯芬减弱了激发期间最大呼气酒精浓度与酒精消耗量之间的正相关(显著交互作用,P = 0.03)。在饮用激发饮料后,巴氯芬组的醉酒感觉评分显著更高(P = 0.006)。在自我给药环节,巴氯芬显著提高了兴奋感评分(P = 0.01)和醉酒感评分(P = 0.01)。在酒精实验室环节中,巴氯芬组还检测到心率显著降低(P < 0.001)以及舒张压有上升趋势(P = 0.06)。总之,巴氯芬被证明会影响焦虑型酒精依赖个体对饮酒的主观和生理反应。这些结果不支持巴氯芬具有抗渴望或抗强化作用,而是表明巴氯芬可能作为酒精使用障碍的替代药物。