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新型驱虫剂阿维菌素B1a增强地西泮的体外结合及某些药理特性。

Enhancement of in vitro binding and some of the pharmacological properties of diazepam by a novel anthelmintic agent, Avermectin B1a.

作者信息

Williams M, Yarbrough G G

出版信息

Eur J Pharmacol. 1979 Jun 15;56(3):273-6. doi: 10.1016/0014-2999(79)90183-3.

Abstract

A novel macrocyclic lactone disaccharide anthelmintic agent, Avermectin B1a (AVM) has been found to cause a concentration-dependent increase in the in vitro binding of 3H-diazepam to rat and mouse brain membranes. The increase in binding is manifested as both an increase in the affinity and number of bindings sites for 3H-diazepam. Preliminary in vivo studies demonstrate that AVM can also enhance some of the pharmacological actions of diazepam.

摘要

一种新型大环内酯二糖驱虫剂阿维菌素B1a(AVM)已被发现会使3H-地西泮与大鼠和小鼠脑膜的体外结合呈浓度依赖性增加。结合的增加表现为3H-地西泮结合位点的亲和力和数量均增加。初步的体内研究表明,AVM还可以增强地西泮的一些药理作用。

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