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非典型抗精神病药物氯氮平的主要活性代谢物N-去甲基氯氮平在C57BL/6小鼠中的辨别性刺激特性。

Discriminative stimulus properties of N-desmethylclozapine, the major active metabolite of the atypical antipsychotic clozapine, in C57BL/6 mice.

作者信息

Wiebelhaus Jason M, Vunck Sarah A, Meltzer Herbert Y, Porter Joseph H

机构信息

Department of Psychology, Virginia Commonwealth University, Richmond, Virginia 23284-2018, USA.

出版信息

Behav Pharmacol. 2012 Jun;23(3):262-70. doi: 10.1097/FBP.0b013e3283534332.

Abstract

N-desmethylclozapine (NDMC) is the major active metabolite of the atypical antipsychotic drug clozapine and may contribute to the therapeutic efficacy of clozapine. Although they share many pharmacological features, it is noteworthy that NDMC is a partial dopamine D2 and cholinergic muscarinic M1/M4 agonist, whereas clozapine is a weak dopamine D2 receptor inverse agonist/antagonist and a nonselective muscarinic antagonist. To better understand the in-vivo pharmacological mechanisms of these drugs, male C57BL/6NHsd-wild-type mice were trained to discriminate 10.0 mg/kg NDMC from vehicle in a two-lever drug discrimination procedure for food reward. It was found that the parent drug clozapine fully substituted for NDMC, whereas the typical antipsychotic drug haloperidol (dopamine D2 antagonist) and the atypical antipsychotic drug aripiprazole (D2 partial agonist) did not substitute for NDMC. These results demonstrated that clozapine and its major metabolite NDMC share in-vivo behavioral properties (i.e. discriminative stimulus properties) that are likely due to shared pharmacological mechanisms that differ from other antipsychotic drugs. The discriminative stimulus properties of NDMC probably reflect a compound cue similar to that of its parent drug clozapine due to its diverse binding profile.

摘要

N-去甲基氯氮平(NDMC)是非典型抗精神病药物氯氮平的主要活性代谢产物,可能对氯氮平的治疗效果有贡献。尽管它们具有许多药理学特征,但值得注意的是,NDMC是多巴胺D2和胆碱能毒蕈碱M1/M4部分激动剂,而氯氮平是一种弱多巴胺D2受体反向激动剂/拮抗剂和非选择性毒蕈碱拮抗剂。为了更好地理解这些药物的体内药理学机制,在一项以食物奖励为目的的双杠杆药物辨别程序中,对雄性C57BL/6NHsd野生型小鼠进行训练,使其能够区分10.0mg/kg的NDMC和溶剂。结果发现,母体药物氯氮平可完全替代NDMC,而典型抗精神病药物氟哌啶醇(多巴胺D2拮抗剂)和非典型抗精神病药物阿立哌唑(D2部分激动剂)不能替代NDMC。这些结果表明,氯氮平及其主要代谢产物NDMC具有共同的体内行为特性(即辨别刺激特性),这可能是由于它们与其他抗精神病药物不同的共同药理学机制所致。由于其多样的结合谱,NDMC的辨别刺激特性可能反映了一种与其母体药物氯氮平相似的复合线索。

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