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The Effects of Naltrexone on Subjective Response to Methamphetamine in a Clinical Sample: a Double-Blind Placebo-Controlled Laboratory Study

机译:纳曲酮对临床样品中对甲基苯丙胺的主观反应的影响:一项双盲安慰剂对照的实验室研究

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摘要

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.
机译:甲基苯丙胺(MA)使用障碍是一种严重的精神疾病,尚无FDA批准的药物。纳曲酮(NTX)是一种阿片受体拮抗剂,具有中等疗效,可治疗酒精中毒和阿片类药物依赖性。临床前和临床研究表明NTX可能对MA使用障碍的治疗有用。为了指导治疗的发展,我们进行了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中关于MA滥用或依赖(n = 30)标准的非治疗患者完成了两次分别为期5天的住院治疗。在每次入院期间,参加者接受口服NTX(50μmg)或安慰剂治疗4天后,完成了由MA提示反应性和静脉内MA给药(30μmg)组成的测试。这项研究检验了NTX会(a)减弱提示引起的MA渴望,以及(b)减少对MA给药的主观反应的假设。结果在很大程度上支持了该研究假说,即(a)NTX显着减弱了提示诱导的对MA的渴望,(b)在控制性MA施用期间以及与安慰剂相比,减弱了MA的几种享乐主观效果,包括渴望。与安慰剂相比,NTX降低了“渴望药物”,“刺激”和“希望获得药物”的总体主观评分,降低了MA后给药后“焦虑”的时程,并提高了“不良药物作用”的评分。这些发现通过表明NTX减少了提示引起的对MA的渴望和主观反应,从而支持了一种潜在的作用机制。这与NTX对苯丙胺依赖的阳性治疗研究以及正在进行的MA的临床试验一致。

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