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氯氮平预处理可增强雷氯必利引起的僵住症。

Clozapine pre-treatment enhances raclopride catalepsy.

作者信息

Wadenberg M L, Seeman P

机构信息

Department of Psychiatry, University of Toronto, Canada.

出版信息

Eur J Pharmacol. 1999 Jul 14;377(1):R1-2. doi: 10.1016/s0014-2999(99)00406-9.

Abstract

The clinical replacement of clozapine by another antipsychotic sometimes causes extrapyramidal signs, including dystonia, to appear suddenly. The present study was done, therefore, to test whether clozapine pre-treatment of rats could affect raclopride-induced catalepsy. Clozapine, at 5 mg/kg, given 2 h before a catalepsy-threshold dose of 0.1 mg/kg raclopride, markedly enhanced raclopride-induced catalepsy in the rats. The results are compatible with earlier in vitro data where pre-exposure of human cloned dopamine D2 receptors to clozapine resulted in an increased potency of raclopride in inhibiting the binding of [3H]clozapine to the receptors. The mechanism of clozapine potentiation of raclopride action may contribute to the clinically observed post-clozapine dystonia.

摘要

用另一种抗精神病药物临床替代氯氮平有时会导致锥体外系症状突然出现,包括肌张力障碍。因此,开展了本研究以测试对大鼠进行氯氮平预处理是否会影响雷氯必利诱发的僵住症。在给予0.1mg/kg雷氯必利(致僵住症阈值剂量)前2小时,给予大鼠5mg/kg氯氮平,可显著增强雷氯必利诱发的大鼠僵住症。这些结果与早期的体外实验数据一致,在该实验中,人克隆多巴胺D2受体预先暴露于氯氮平会导致雷氯必利抑制[3H]氯氮平与受体结合的效力增强。氯氮平增强雷氯必利作用的机制可能与临床上观察到的氯氮平停药后肌张力障碍有关。

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