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氟哌啶醇所致的僵住症受钙通道拮抗剂的影响。

Haloperidol-induced catalepsy is influenced by calcium channel antagonists.

作者信息

Biała G

机构信息

Department of Pharmacodynamics, Medical University, 20-081 Lublin, 4 Staszica Str., Poland.

出版信息

Acta Pol Pharm. 2000 May-Jun;57(3):233-7.

Abstract

The effect of pretreatment of some voltage-dependent calcium channel antagonists was studied on haloperidol-induced catalepsy in male Wistar rats. Cataleptogenic effect of haloperidol (0.25 mg/kg, i.p.) was enhanced dose-dependently by nitrendipine (5, 10 and 20 mg/kg, i.p.) and the highest dose of nimodipine (20 mg/kg, i.p.). Neither verapamil (10 and 20 mg/kg, i.p.) nor diltiazem (10 and 20 mg/kg, i.p.) influenced the score of haloperidol-induced catalepsy in rats. These results suggest the involvement of calcium-dependent mechanisms in the generation of haloperidol-induced catalepsy. The possible involvement of dopaminergic mechanisms and modification by calcium channel antagonists are discussed.

摘要

研究了一些电压依赖性钙通道拮抗剂预处理对雄性Wistar大鼠中氟哌啶醇诱导的僵住症的影响。硝苯地平(5、10和20mg/kg,腹腔注射)和最高剂量的尼莫地平(20mg/kg,腹腔注射)可使氟哌啶醇(0.25mg/kg,腹腔注射)的致僵作用剂量依赖性增强。维拉帕米(10和20mg/kg,腹腔注射)和地尔硫䓬(10和20mg/kg,腹腔注射)均未影响大鼠中氟哌啶醇诱导的僵住症评分。这些结果表明钙依赖性机制参与了氟哌啶醇诱导的僵住症的产生。讨论了多巴胺能机制的可能参与以及钙通道拮抗剂的修饰作用。

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