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