首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Striatal and nigral COX-2 expression after chronic typical and atypical neuroleptic administration in rats.
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Striatal and nigral COX-2 expression after chronic typical and atypical neuroleptic administration in rats.

机译:慢性典型和非典型抗精神病药物给药后大鼠的纹状体和黑质COX-2表达。

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摘要

Haloperidol, but not clozapine, induces dopaminergic nigrostriatal degeneration. However, the mechanisms by which haloperidol causes neurotoxicity are not fully understood. An increase in cyclooxygenase-2 (COX-2) expression has been observed correlated with nigrostriatal degeneration. We investigated the modifications of striatal and nigral COX-2 expression induced by chronic haloperidol and clozapine administration. Rats were treated for 21 days with: haloperidol (1 mg/kg), clozapine (1 mg/kg) or saline. No significant differences were observed in striatal and nigral COX-2 expression between haloperidol and clozapine-treated animals. This observation might suggest that nigral COX-2 expression is not the underlying mechanisms involved in haloperidol-induced dopaminergic neurodegeneration.
机译:氟哌啶醇而不是氯氮平诱导多巴胺能黑质纹状体变性。但是,氟哌啶醇引起神经毒性的机制尚未完全了解。已经观察到环氧合酶-2(COX-2)表达的增加与黑纹状体变性相关。我们调查了慢性氟哌啶醇和氯氮平给药引起的纹状体和黑质COX-2表达的修饰。用氟哌啶醇(1 mg / kg),氯氮平(1 mg / kg)或生理盐水治疗大鼠21天。氟哌啶醇和氯氮平治疗的动物之间纹状体和黑质COX-2表达未见明显差异。该观察结果可能表明,黑色素COX-2的表达不是氟哌啶醇诱导的多巴胺能神经变性的潜在机制。

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