Berro Laís F, Andersen Monica L, Howell Leonard L
Yerkes National Primate Research Center, Emory University, 954 Gatewood Road N.E, Atlanta, GA, 30329, USA.
Department of Psychobiology, Universidade Federal de São Paulo, R. Napoleão de Barros, 925, São Paulo, SP, 04021002, Brazil.
Psychopharmacology (Berl). 2017 Aug;234(15):2277-2287. doi: 10.1007/s00213-017-4654-1. Epub 2017 Jun 7.
Methamphetamine is one of the most largely consumed illicit drugs, and its use is associated with abuse liability and several adverse health effects, such as sleep impairment. Importantly, sleep quality can influence addiction treatment outcomes. Evidence suggests that tolerance can develop to the sleep-disrupting effects of stimulant drugs.
The aim of the present study was to investigate the development of tolerance to the actigraphy-based sleep-disrupting and stimulant effects of methamphetamine self-administration in rhesus monkeys.
Methamphetamine (0.03 mg/kg/inf, i.v.) self-administration was carried out following three different protocols: 14 consecutive days of self-administration, 5 days/week for 3 weeks, with a 2-day interval between 5-day blocks of self-administration, and 3 days/week for 3 weeks, with a 4-day interval between 3-day blocks of self-administration. Daytime activity and activity-based sleep measures were evaluated with Actiwatch monitors a week before (baseline parameters) and throughout each protocol.
Methamphetamine self-administration markedly disrupted sleep-like measures and increased daytime activity. Tolerance developed to those effects with repeated methamphetamine intake exceeding five consecutive days. Inclusion of washout periods (2 or 4 days) between blocks of methamphetamine self-administration attenuated the development of tolerance, with longer breaks from methamphetamine intake being more effective in maintaining the sleep-disrupting and stimulant effects of methamphetamine.
Tolerance can develop to the stimulant and sleep-disrupting effects of methamphetamine self-administration. Interruption of drug intake extends the effects of methamphetamine on sleep-like measures and daytime activity.
甲基苯丙胺是消费最为广泛的非法药物之一,其使用与成瘾倾向及多种不良健康影响相关,如睡眠障碍。重要的是,睡眠质量会影响成瘾治疗效果。有证据表明,对兴奋剂药物的睡眠干扰作用会产生耐受性。
本研究旨在探讨恒河猴对甲基苯丙胺自我给药基于活动记录仪的睡眠干扰和兴奋作用的耐受性发展情况。
按照三种不同方案进行甲基苯丙胺(0.03毫克/千克/次,静脉注射)自我给药:连续14天自我给药;每周5天,共3周,在5天给药阶段之间间隔2天;每周3天,共3周,在3天给药阶段之间间隔4天。在每个方案实施前一周(基线参数)及整个过程中,使用活动记录仪监测仪评估白天活动和基于活动的睡眠指标。
甲基苯丙胺自我给药显著扰乱了类似睡眠的指标并增加了白天活动。连续五天以上重复摄入甲基苯丙胺会产生对这些作用的耐受性。在甲基苯丙胺自我给药阶段之间加入洗脱期(2天或4天)可减弱耐受性的发展,甲基苯丙胺摄入间隔时间越长,对维持甲基苯丙胺的睡眠干扰和兴奋作用越有效。
对甲基苯丙胺自我给药的兴奋和睡眠干扰作用可产生耐受性。药物摄入的中断会延长甲基苯丙胺对类似睡眠指标和白天活动的影响。