University of Kentucky College of Medicine, Department of Behavioral Science, 140 Medical Behavioral Science Building, Lexington, KY 40536-0086, United States; University of Kentucky College of Arts and Sciences, Department of Psychology, 110 Kastle Hall, Lexington, KY 40506-0044, United States.
Prog Neuropsychopharmacol Biol Psychiatry. 2013 Dec 2;47:111-7. doi: 10.1016/j.pnpbp.2013.08.007. Epub 2013 Aug 28.
Methamphetamine use disorders remain a significant public health concern. Methamphetamine produces its behavioral effects by facilitating release of monoamines like dopamine (DA) and serotonin (5-HT). Results from animal studies show that acute pretreatment with DA and 5-HT antagonists attenuates the effects of methamphetamine, but this area remains largely unexplored in humans. This study sought to assess whether aripiprazole, a partial agonist at D2/5-HT1A receptors and an antagonist at 5-HT2A receptors, would attenuate the reinforcing and subject-rated effects of oral methamphetamine. Seven subjects with histories of recreational stimulant use completed a placebo-controlled, crossover, double-blind protocol in which they first sampled doses of oral methamphetamine (0, 4, 8 or 16 mg) following acute pretreatment with aripiprazole (0 and 15 mg). During each Sampling Session, subjects also completed a battery of subject-rated, cardiovascular, and other performance measures. In subsequent Self-Administration Sessions, subjects were provided the opportunity to earn the previously sampled methamphetamine dose on a progressive-ratio procedure. Methamphetamine functioned as a reinforcer, and produced prototypical stimulant-like subject-rated and cardiovascular effects (e.g., increased ratings of Stimulated; elevated blood pressure). Aripiprazole reduced methamphetamine self-administration and attenuated some of the positive subject-rated effects of methamphetamine (e.g., ratings of Like Drug). These results indicate that acute aripiprazole pretreatment attenuates the abuse-related effects of methamphetamine.
甲基苯丙胺使用障碍仍然是一个重大的公共卫生问题。甲基苯丙胺通过促进多巴胺(DA)和 5-羟色胺(5-HT)等单胺类物质的释放来产生其行为效应。动物研究的结果表明,DA 和 5-HT 拮抗剂的急性预处理可减弱甲基苯丙胺的作用,但这一领域在人类中仍未得到广泛探索。本研究旨在评估阿立哌唑(D2/5-HT1A 受体的部分激动剂和 5-HT2A 受体的拮抗剂)是否会减弱口服甲基苯丙胺的强化和受试者自评效应。7 名有娱乐性兴奋剂使用史的受试者完成了一项安慰剂对照、交叉、双盲方案,他们首先在阿立哌唑(0 和 15 毫克)急性预处理后,接受了不同剂量的口服甲基苯丙胺(0、4、8 或 16 毫克)的采样。在每次采样过程中,受试者还完成了一系列自评、心血管和其他表现测量。在随后的自我给药过程中,受试者有机会通过逐步递增比率程序获得之前采样的甲基苯丙胺剂量。甲基苯丙胺作为一种强化物,产生了典型的兴奋剂样的自评和心血管效应(例如,增加刺激感评分;血压升高)。阿立哌唑降低了甲基苯丙胺的自我给药量,并减弱了甲基苯丙胺的一些阳性自评效应(例如,对药物的喜欢程度评分)。这些结果表明,急性阿立哌唑预处理可减弱甲基苯丙胺的滥用相关效应。