Preclinical Pharmacology Section, Behavioral Neuroscience Branch, DHHS/NIH/NIDA Intramural Research Program, 251 Bayview Blvd., Suite 200, Baltimore, MD 21224, United States.
Eur J Pharmacol. 2010 May 10;633(1-3):44-9. doi: 10.1016/j.ejphar.2010.02.005. Epub 2010 Feb 11.
Cannabinoid receptor antagonists have shown some promise as treatments capable of reducing abuse and relapse to a number of abused drugs. In rodents, such effects have been observed with methamphetamine self-administration. However, the effects of cannabinoid receptor antagonists on methamphetamine self-administration and relapse have not been studied in primates. In the present study, rhesus monkeys were trained to respond on a three-component operant schedule. During the first 5-min component, fixed-ratio responses were reinforced by food, during the second 90- or 180-min component fixed-ratio responses were reinforced by i.v. methamphetamine. The third component was identical to the first. There was a 5-min timeout between each component. The effects of the cannabinoid receptor antagonists AM 251 and rimonabant were tested at various doses against self-administration of 3microg/kg/injection methamphetamine, and 1mg/kg AM 251 and 0.3mg/kg rimonabant were tested against the methamphetamine dose-effect function. The 1mg/kg dose of AM 251 was also tested for its ability to alter reinstatement of extinguished self-administration responding. The cannabinoid receptor antagonist AM 251 was found to reduce methamphetamine self-administration at doses that did not affect food-reinforced responding. The cannabinoid receptor antagonist rimonabant had similar, but less robust effects. AM 251 also prevented reinstatement of extinguished methamphetamine seeking that was induced by re-exposure to a combination of methamphetamine and methamphetamine-associated cues. These results indicate that cannabinoid receptor antagonists might have therapeutic effects for the treatment of methamphetamine dependence.
大麻素受体拮抗剂作为能够减少滥用和对多种滥用药物的复发的治疗方法显示出了一定的前景。在啮齿动物中,这种效应已经在 methamphetamine 自我给药中观察到。然而,大麻素受体拮抗剂对 methamphetamine 自我给药和复发的影响在灵长类动物中尚未得到研究。在本研究中,恒河猴接受了三成分操作性条件反射训练。在第一个 5 分钟的成分中,固定比率反应通过食物得到强化,在第二个 90 或 180 分钟的成分中,固定比率反应通过静脉内给予 methamphetamine 得到强化。第三个成分与第一个成分相同。每个成分之间有 5 分钟的时间间隔。在不同剂量下测试了大麻素受体拮抗剂 AM 251 和 rimonabant 对 3microg/kg/注射 methamphetamine 的自我给药的影响,并测试了 1mg/kg AM 251 和 0.3mg/kg rimonabant 对 methamphetamine 剂量效应函数的影响。还测试了 1mg/kg 的 AM 251 对消除自我给药反应的复燃的影响。大麻素受体拮抗剂 AM 251 在不影响食物强化反应的剂量下降低了 methamphetamine 的自我给药。大麻素受体拮抗剂 rimonabant 具有类似但较弱的作用。AM 251 还防止了由于重新暴露于 methamphetamine 和与 methamphetamine 相关的线索的组合而引起的已消除的 methamphetamine 寻求的复燃。这些结果表明,大麻素受体拮抗剂可能对治疗 methamphetamine 依赖具有治疗效果。