Kayir Hakan, Goktalay Gokhan, Yildirim Murat, Uzbay Tayfun I
Department of Medical Pharmacology, Psychopharmacology Research Unit, Gulhane Military Medical Academy, Ankara, Turkey.
Synapse. 2009 Jan;63(1):15-21. doi: 10.1002/syn.20576.
It has been shown that clozapine, the prototype of atypical antipsychotics, significantly reduces daily cigarette use and alcohol consumption in schizophrenic patients. However, our knowledge about the effect of clozapine on nicotine abuse is limited. Aim of this study was to determine whether clozapine would inhibit the development and expression of nicotine-induced locomotor sensitization in rats. To investigate the effect of clozapine on the development of nicotine-induced locomotor sensitization, rats were pretreated with clozapine (2.5-10 mg/kg) 30 min before the nicotine (0.5 mg/kg), and locomotor activity was recorded for 15 min. This procedure was repeated every day for eight sessions. After a 3-day drug-free period, rats were challenged with nicotine (0.5 mg/kg). To reveal effect of clozapine on the expression of nicotine-induced locomotor sensitization, rats were injected with nicotine for eight sessions. After a 3-day drug-free period, rats were pretreated with clozapine (2.5-10 mg/kg) or vehicle 30 min before the nicotine (0.5 mg/kg) challenge injection. Repeated administration of nicotine generated robust locomotor sensitization in rats. Clozapine pretreatment (2.5-10 mg/kg) blocked the development and the expression of nicotine-induced locomotor sensitization in rats. Our results suggest that atypical antipsychotic clozapine can prevent the effects of nicotine in an animal model of dependence, which represents early adaptations in initiation and continuation of addictive behavior.
已有研究表明,非典型抗精神病药物的原型氯氮平可显著减少精神分裂症患者的每日吸烟量和酒精摄入量。然而,我们对氯氮平对尼古丁滥用影响的了解有限。本研究的目的是确定氯氮平是否会抑制大鼠尼古丁诱导的运动敏化的发展和表达。为了研究氯氮平对尼古丁诱导的运动敏化发展的影响,在给予尼古丁(0.5mg/kg)前30分钟,用氯氮平(2.5 - 10mg/kg)预处理大鼠,并记录15分钟的运动活性。此过程每天重复进行,共八次。在3天的无药期后,用尼古丁(0.5mg/kg)对大鼠进行激发试验。为了揭示氯氮平对尼古丁诱导的运动敏化表达的影响,对大鼠注射尼古丁,共八次。在3天的无药期后,在尼古丁(0.5mg/kg)激发注射前30分钟,用氯氮平(2.5 - 10mg/kg)或赋形剂预处理大鼠。重复给予尼古丁可使大鼠产生强烈的运动敏化。氯氮平预处理(2.5 - 10mg/kg)可阻断大鼠尼古丁诱导的运动敏化的发展和表达。我们的结果表明,非典型抗精神病药物氯氮平可以在依赖动物模型中预防尼古丁的作用,这代表了成瘾行为起始和持续过程中的早期适应性变化。