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新型血管紧张素转换酶抑制剂盐酸贝那普利的一般药理学。对中枢神经和感觉系统及其他功能的影响。

General pharmacology of the novel angiotensin converting enzyme inhibitor benazepril hydrochloride. Effects on central nervous and sensory systems and other functions.

作者信息

Yamamoto S, Takemori E, Hasegawa Y, Nakao K, Inukai T, Nomura M, Morino K, Tsuchiyama M, Hasegawa K, Ikeda H

机构信息

Pre-clinical Research Department, Ciba-Geigy Limited, Takarazuka, Japan.

出版信息

Arzneimittelforschung. 1991 Jun;41(6):602-7.

PMID:1930347
Abstract

The effects of benazepril hydrochloride (CGS 14824 A, CAS 86541-74-4), a novel angiotension I converting enzyme inhibitor, on the central nervous systems, were studied in experimental animals. Benazepril hydrochloride (3 or 10 mg/kg/d, p.o. for 14 days) dose-dependently inhibited the increase in the blood pressure caused by continuous norepinephrine (NE) infusion in spontaneously hypertensive rats (SHR) and suppressed in seizures induced by a monoamine oxidase inhibitor, tranylcypromine in NE infused SHR. Benazepril hydrochloride transiently increased spontaneous motor activity in mice, tended to inhibit acetic acid-induced writhing in mice and decreased fast wave sleep and slow wave deep sleep on EEG in cats at a high dose of 100 mg/kg p.o. However, benazepril hydrochloride at the same dose showed no effect on other central nervous and sensory systems in experimental animals.

摘要

在实验动物中研究了新型血管紧张素I转换酶抑制剂盐酸贝那普利(CGS 14824 A,CAS 86541-74-4)对中枢神经系统的作用。盐酸贝那普利(3或10毫克/千克/天,口服,持续14天)剂量依赖性地抑制自发性高血压大鼠(SHR)中持续输注去甲肾上腺素(NE)引起的血压升高,并抑制在输注NE的SHR中由单胺氧化酶抑制剂反苯环丙胺诱发的癫痫发作。盐酸贝那普利使小鼠的自发运动活性短暂增加,倾向于抑制小鼠中乙酸诱导的扭体反应,并在口服高剂量100毫克/千克时减少猫脑电图中的快波睡眠和慢波深睡眠。然而,相同剂量的盐酸贝那普利对实验动物的其他中枢神经和感觉系统没有影响。

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