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两种单环β-内酰胺衍生物在C57、瑞士和DBA/2小鼠中的致癫痫特性比较

Comparative epileptogenic properties of two monobactam derivatives in C57, Swiss and DBA/2 mice.

作者信息

De Sarro A, Naccari F, Imperatore C, De Sarro G B

机构信息

Institute of Pharmacology, School of Medicine, Piazza XX Settembre 4, Messina, Italy.

出版信息

J Antimicrob Chemother. 1996 Sep;38(3):475-84. doi: 10.1093/jac/38.3.475.

Abstract

The behavioural and electrocortical effects of two monobactam derivatives were studied after intraperitoneal (ip) administration in DBA/2 mice, a strain genetically susceptible to sound-induced seizures, and in C57 and Swiss mice, two strains not prone to seizure. DBA/2 mice were more susceptible than Swiss and C57 mice to seizures induced by aztreonam or carumonam. No significant differences were observed between seizures elicited by aztreonam and carumonam in animals (DBA/2 only) administered intracerebroventricularly or ip. Although the main mechanism for seizure-like activity of monobactams cannot be easily determined, we believe that several mechanisms may be involved. An increased excitation of the central nervous system (CNS) by inhibition of GABA binding to receptors and a slow clearance of aztreonam and carumonam from the CNS may be postulated.

摘要

在对DBA/2小鼠(一种对声音诱发癫痫遗传易感的品系)、C57小鼠和瑞士小鼠(两种不易发生癫痫的品系)进行腹腔注射后,研究了两种单环β-内酰胺衍生物的行为和皮层电效应。DBA/2小鼠比瑞士小鼠和C57小鼠更容易受到氨曲南或卡芦莫南诱发的癫痫发作影响。在经脑室内或腹腔注射给药的动物(仅DBA/2)中,氨曲南和卡芦莫南诱发的癫痫发作之间未观察到显著差异。虽然单环β-内酰胺类药物癫痫样活动的主要机制不易确定,但我们认为可能涉及多种机制。可以推测,通过抑制GABA与受体的结合增加中枢神经系统(CNS)的兴奋性,以及氨曲南和卡芦莫南从CNS的缓慢清除可能是其原因。

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