Alcohol and Drug Abuse Research Center, McLean Hospital-Harvard Medical School, Belmont, MA, USA.
Center for Organic and Medicinal Chemistry, Research Triangle Institute, Research Triangle Park, NC, USA.
Neuropsychopharmacology. 2014 Apr;39(5):1222-31. doi: 10.1038/npp.2013.325. Epub 2013 Nov 22.
Nicotine dependence and cocaine abuse are major public health problems, and most cocaine abusers also smoke cigarettes. An ideal treatment medication would reduce both cigarette smoking and cocaine abuse. Varenicline is a clinically available, partial agonist at α4β2* and α6β2* nicotinic acetylcholine receptors (nAChRs) and a full agonist at α7 nAChRs. Varenicline facilitates smoking cessation in clinical studies and reduced nicotine self-administration, and substituted for the nicotine-discriminative stimulus in preclinical studies. The present study examined the effects of chronic varenicline treatment on self-administration of IV nicotine, IV cocaine, IV nicotine+cocaine combinations, and concurrent food-maintained responding by five cocaine- and nicotine-experienced adult rhesus monkeys (Macaca mulatta). Varenicline (0.004-0.04 mg/kg/h) was administered intravenously every 20 min for 23 h each day for 7-10 consecutive days. Each varenicline treatment was followed by saline-control treatment until food- and drug-maintained responding returned to baseline. During control treatment, nicotine+cocaine combinations maintained significantly higher levels of drug self-administration than nicotine or cocaine alone (P<0.05-0.001). Varenicline dose-dependently reduced responding maintained by nicotine alone (0.0032 mg/kg/inj) (P<0.05), and in combination with cocaine (0.0032 mg/kg/inj) (P<0.05) with no significant effects on food-maintained responding. However, varenicline did not significantly decrease self-administration of a low dose of nicotine (0.001 mg/kg), cocaine alone (0.0032 and 0.01 mg/kg/inj), or 0.01 mg/kg cocaine combined with the same doses of nicotine. We conclude that varenicline selectively attenuates the reinforcing effects of nicotine alone but not cocaine alone, and its effects on nicotine+cocaine combinations are dependent on the dose of cocaine.
尼古丁依赖和可卡因滥用是主要的公共卫生问题,大多数可卡因滥用者也吸烟。一种理想的治疗药物应该能够减少吸烟和可卡因滥用。伐伦克林是一种临床可用的α4β2和α6β2烟碱型乙酰胆碱受体(nAChRs)部分激动剂和α7 nAChRs完全激动剂。伐伦克林在临床研究中促进戒烟,并减少尼古丁自我给药,并在临床前研究中替代尼古丁辨别刺激。本研究检查了慢性伐伦克林治疗对静脉内尼古丁、静脉内可卡因、静脉内尼古丁+可卡因组合以及由五只可卡因和尼古丁经验丰富的成年恒河猴(Macaca mulatta)维持的同时食物反应的自我给药的影响。伐伦克林(0.004-0.04mg/kg/h)每天静脉内每 20 分钟给药一次,持续 23 小时,连续 7-10 天。在每种伐伦克林治疗后,用生理盐水对照治疗,直到食物和药物维持的反应恢复到基线。在对照治疗期间,尼古丁+可卡因组合维持的药物自我给药水平明显高于尼古丁或可卡因单独给药(P<0.05-0.001)。伐伦克林剂量依赖性地降低了尼古丁单独给药(0.0032mg/kg/注射)(P<0.05)和与可卡因联合给药(0.0032mg/kg/注射)(P<0.05)的反应,对食物维持的反应没有显著影响。然而,伐伦克林并没有显著减少低剂量尼古丁(0.001mg/kg)、单独可卡因(0.0032 和 0.01mg/kg/注射)或 0.01mg/kg 可卡因与相同剂量尼古丁的联合自我给药。我们的结论是,伐伦克林选择性地减弱了尼古丁单独给药的强化作用,但不能减弱可卡因单独给药的强化作用,其对尼古丁+可卡因组合的作用取决于可卡因的剂量。