Ray Lara A, Bujarski Spencer, Courtney Kelly E, Moallem Nathasha R, Lunny Katy, Roche Daniel, Leventhal Adam M, Shoptaw Steve, Heinzerling Keith, London Edythe D, Miotto Karen
1] Department of Psychology, University of California, Los Angeles, Los Angeles, CA, USA [2] Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, USA.
Department of Psychology, University of California, Los Angeles, Los Angeles, CA, USA.
Neuropsychopharmacology. 2015 Sep;40(10):2347-56. doi: 10.1038/npp.2015.83. Epub 2015 Mar 24.
Methamphetamine (MA) use disorder is a serious psychiatric condition for which there are no FDA-approved medications. Naltrexone (NTX) is an opioid receptor antagonist with demonstrated efficacy, albeit moderate, for the treatment of alcoholism and opioid dependence. Preclinical and clinical studies suggest that NTX may be useful for the treatment of MA use disorder. To inform treatment development, we conducted a double-blind, randomized, crossover, placebo-controlled human laboratory study of NTX. Non-treatment-seeking individuals meeting DSM-IV criteria for MA abuse or dependence (n=30) completed two separate 5-day inpatient stays. During each admission, participants completed testing sessions comprised of MA cue-reactivity and intravenous MA administration (30 mg) after receiving oral NTX (50 mg) or placebo for 4 days. This study tested the hypotheses that NTX would (a) attenuate cue-induced MA craving, and (b) reduce subjective responses to MA administration. Results largely supported the study hypotheses such that (a) NTX significantly blunted cue-induced craving for MA and (b) attenuated several of the hedonic subjective effects of MA, including craving, during controlled MA administration and as compared with placebo. NTX decreased overall subjective ratings of 'crave drug,' 'stimulated,' and 'would like drug access,' decreased the the post-MA administration timecourse of 'anxious' and increased ratings of 'bad drug effects,' as compared with placebo. These findings support a potential mechanism of action by showing that NTX reduced cue-induced craving and subjective responses to MA. This is consistent with positive treatment studies of NTX for amphetamine dependence, as well as ongoing clinical trials for MA.
甲基苯丙胺(MA)使用障碍是一种严重的精神疾病,目前尚无美国食品药品监督管理局(FDA)批准的治疗药物。纳曲酮(NTX)是一种阿片受体拮抗剂,已证明对治疗酒精中毒和阿片类药物依赖有效,尽管效果一般。临床前和临床研究表明,NTX可能对治疗MA使用障碍有用。为了为治疗开发提供信息,我们进行了一项关于NTX的双盲、随机、交叉、安慰剂对照的人体实验室研究。符合DSM-IV标准的MA滥用或依赖且未寻求治疗的个体(n = 30)完成了两次单独的为期5天的住院治疗。在每次住院期间,参与者在接受口服NTX(50毫克)或安慰剂4天后完成了由MA线索反应性和静脉注射MA(30毫克)组成的测试环节。本研究检验了以下假设:(a)NTX会减轻线索诱导的MA渴望,以及(b)降低对MA给药的主观反应。结果在很大程度上支持了研究假设,即(a)NTX显著减弱了线索诱导的对MA的渴望;(b)在MA给药受控期间,与安慰剂相比,NTX减弱了MA的几种享乐主义主观效应,包括渴望。与安慰剂相比,NTX降低了“渴望药物”“兴奋”和“希望获得药物”的总体主观评分;降低了MA给药后“焦虑”的时间进程,并提高了“药物不良反应”的评分。这些发现通过表明NTX减少了线索诱导的渴望和对MA的主观反应,支持了一种潜在的作用机制。这与NTX治疗苯丙胺依赖的阳性治疗研究以及正在进行的MA临床试验一致。