Suppr超能文献

亮氨酸脑啡肽具有麻醉激动特性的新体内证据。

New in vivo evidence for narcotic agonistic property of leucine-enkephalin.

作者信息

Bhargava H N

出版信息

J Pharm Sci. 1978 Jan;67(1):136-7. doi: 10.1002/jps.2600670141.

Abstract

Administration of leucine-enkephalin or morphine to mice rendered dependent on morphine by pellet implantation inhibited the naloxone-precipitated abstinence syndrome. The withdrawal jumping response was inhibited by morphine or leucine-enkephalin; however, both failed to inhibit withdrawal defecation and rearing behavior. On a molar basis, leucine-enkephalin was half as potent as morphine in inhibiting the abstinence syndrome. New in vivo pharmacological evidence for narcotic agonist-like activity of leucine-enkephalin is provided.

摘要

通过植入药丸使小鼠对吗啡产生依赖后,给这些小鼠注射亮氨酸脑啡肽或吗啡,可抑制纳洛酮诱发的戒断综合征。吗啡或亮氨酸脑啡肽可抑制戒断跳跃反应;然而,二者均未能抑制戒断时的排便和竖毛行为。以摩尔为基础计算,亮氨酸脑啡肽在抑制戒断综合征方面的效力仅为吗啡的一半。本文提供了亮氨酸脑啡肽具有类麻醉激动剂活性的新的体内药理学证据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验