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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Clozapine and other 5-hydroxytryptamine-2A receptor antagonists alter the subcellular distribution of 5-hydroxytryptamine-2A receptors in vitro and in vivo.
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Clozapine and other 5-hydroxytryptamine-2A receptor antagonists alter the subcellular distribution of 5-hydroxytryptamine-2A receptors in vitro and in vivo.

机译:氯氮平和其他5-羟色胺2A受体拮抗剂在体外和体内均可改变5-羟色胺2A受体的亚细胞分布。

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摘要

In this study, we demonstrate that clozapine and other atypical antipsychotic drugs induce a paradoxical internalization of 5-hydroxytryptamine-2A receptors in vitro and a redistribution of 5-hydroxytryptamine-2A receptors in vivo. We discovered that clozapine, olanzapine, risperidone and the putative atypical antipsychotic drug MDL 100,907 all induced 5-hydroxytryptamine-2A receptor internalization in fibroblasts stably expressing the 5-hydroxytryptamine-2A receptor in vitro. Two 5-hydroxytryptamine-2A antagonists (mianserin and ritanserin), which have been demonstrated to reduce negative symptoms in schizophrenia, also caused 5-hydroxytryptamine-2A receptor internalization. Four different drugs, each devoid of 5-hydroxytryptamine-2A antagonist activity, had no effect on the subcellular distribution of 5-hydroxytryptamine-2A receptors in vitro. Treatment of rats for seven days with clozapine induced an increase in intracellular 5-hydroxytryptamine-2A receptor-like immunoreactivity in pyramidal neurons, while causing a decrease in labeling of apical dendrites in the medial prefrontal cortex. This redistribution of 5-hydroxytryptamine-2A receptors in pyramidal neurons was also seen when rats were chronically treated with another atypical antipsychotic drug, olanzapine. The typical antipsychotic drug haloperidol, however, did not induce a redistribution of 5-hydroxytryptamine-2A receptors in pyramidal neurons in the medial prefrontal cortex. Taken together, these results demonstrate that several atypical antipsychotic drugs with high 5-hydroxytryptamine-2A receptor affinities induce a redistribution of 5-hydroxytryptamine-2A receptors both in vivo and in vitro. It is conceivable that the loss of 5-hydroxytryptamine-2A receptors from the apical dendrites of pyramidal neurons is important for the beneficial effects of atypical antipsychotic drugs and other 5-hydroxytryptamine-2A antagonists in schizophrenia.
机译:在这项研究中,我们证明了氯氮平和其他非典型抗精神病药在体外诱导5-羟色胺2A受体的反常内在化和在体内5-羟色胺2A受体的重新分布。我们发现氯氮平,奥氮平,利培酮和公认的非典型抗精神病药物MDL 100907均可诱导成纤维细胞中5-羟基色胺2A受体的内在化,在体外稳定表达5-羟基色胺2A受体。两种5-羟色胺-2A拮抗剂(米安色林和利坦色林)已被证明可减轻精神分裂症的不良症状,也引起5-羟色胺-2A受体的内在化。四种不同的药物,每种药物都没有5-羟色胺2A拮抗剂的活性,对5-羟色胺2A受体的亚细胞分布在体外没有影响。用氯氮平治疗大鼠7天后,锥体神经元细胞内5-羟色胺2A受体样免疫反应性增加,同时引起内侧前额叶皮层顶突的标记减少。当大鼠用另一种非典型抗精神病药物奥氮平进行慢性治疗时,也看到了锥体神经元中5-羟色胺-2A受体的这种重新分布。然而,典型的抗精神病药物氟哌啶醇在前额叶内侧皮质的锥体神经元中不会诱导5-羟色胺2A受体的重新分布。综上所述,这些结果表明,具有高5-羟色胺-2A受体亲和力的几种非典型抗精神病药可在体内和体外诱导5-羟色胺-2A受体的重新分布。可以想象,锥体神经元根尖树突中5-羟色胺-2A受体的丧失对于非典型抗精神病药和其他5-羟色胺-2A拮抗剂在精神分裂症中的有益作用是重要的。

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