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维脑路通的抗紧张症作用。

Anticatatonic effect of venoruton.

作者信息

Aley K O, Kulkarni S K

机构信息

Department of Pharmaceutical Sciences, Panjab University, Chandigarh, India.

出版信息

Methods Find Exp Clin Pharmacol. 1988 Apr;10(4):263-5.

PMID:2898576
Abstract

The protective effect of venoruton O-(beta-hydroxy-ethyl) rutoside, HR was investigated against drug induced catatonia in rats. Perphenazine, haloperidol, reserpine and meperidine produced frank catalepsy in rats. The cataleptic effect of these neuroleptics was significantly attenuated when the animals were pretreated with venoruton. The protective effect of venoruton is speculated to be due to its inhibitory action on superoxide formation and free radicals are considered to have a role in the neurotoxicity caused by the above agents.

摘要

研究了维脑路通(曲克芦丁,O-(β-羟乙基)芦丁)对大鼠药物诱导的紧张症的保护作用。奋乃静、氟哌啶醇、利血平和哌替啶可使大鼠出现明显的僵住症。当动物预先用维脑路通处理时,这些抗精神病药物的僵住效应显著减弱。推测维脑路通的保护作用是由于其对超氧化物形成的抑制作用,并且自由基被认为在上述药物引起的神经毒性中起作用。

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