Villégier Anne-Sophie, Lotfipour Shahrdad, McQuown Susan C, Belluzzi James D, Leslie Frances M
Department of Pharmacology, School of Medicine, University of California, Irvine, CA 92697, USA.
Neuropharmacology. 2007 May;52(6):1415-25. doi: 10.1016/j.neuropharm.2007.02.001. Epub 2007 Feb 20.
Tobacco use has one of the highest rates of addiction of any abused drug. Paradoxically, in animal models, nicotine appears to be a weak reinforcer. We report here that the inhibition of monoamine oxidase (MAO), a major effect of tobacco smoke, increases the reinforcing effect of nicotine. Rats (aged postnatal day 27 and 90) were tested for self-administration, without prior response training, in five daily 3-h sessions. Whereas control rats did not self-administer nicotine, low doses of nicotine (2.5 to 21 microg/kg/injection) were avidly self-administered following a pretreatment with tranylcypromine (3 mg/kg), an irreversible and non-selective MAO inhibitor. Tranylcypromine-enhanced nicotine (10 microg/kg/injection, i.v.) self-administration was reduced by systemic injection of a D1-dopaminergic receptor antagonist, SCH23390 (0.02 mg/kg). Moreover, an increase in extracellular dopamine in the nucleus accumbens was detected, using microdialysis, following nicotine (60 microg/kg) injection in tranylcypromine pre-treated rats. Depending on the time of tranylcypromine pretreatment (20 or 1 h), MAO activity was decreased by 72% and 99% and nicotine intake at day 5 was increased by 619 and 997%, respectively. Taken together, these results indicate that in a stringent self-administration acquisition test, MAO inhibition increases the rewarding effect of low doses of nicotine, possibly via a dopamine-dependent mechanism.
在所有滥用药物中,烟草使用的成瘾率是最高的之一。矛盾的是,在动物模型中,尼古丁似乎是一种较弱的强化剂。我们在此报告,烟草烟雾的主要作用——单胺氧化酶(MAO)的抑制,会增强尼古丁的强化作用。对出生后第27天和90天的大鼠进行自我给药测试,无需事先进行反应训练,每天进行5次,每次3小时。对照大鼠不会自我给药尼古丁,而在用反苯环丙胺(3毫克/千克)进行预处理后,低剂量的尼古丁(2.5至21微克/千克/注射)会被大鼠积极地自我给药,反苯环丙胺是一种不可逆且非选择性的MAO抑制剂。全身性注射D1 - 多巴胺能受体拮抗剂SCH23390(0.02毫克/千克)可降低反苯环丙胺增强的尼古丁(10微克/千克/注射,静脉注射)自我给药行为。此外,在反苯环丙胺预处理的大鼠中注射尼古丁(60微克/千克)后,通过微透析检测到伏隔核细胞外多巴胺增加。根据反苯环丙胺预处理的时间(20或1小时),MAO活性分别降低了72%和99%,第5天的尼古丁摄入量分别增加了619%和997%。综上所述,这些结果表明,在严格的自我给药获取测试中,MAO抑制可能通过多巴胺依赖机制增强低剂量尼古丁的奖赏作用。