鸦片剂
兴奋剂
化学
敌手
(+)-纳洛酮
药理学
受体
阿片受体
体内
结合位点
体外
内科学
内分泌学
医学
生物
生物化学
生物技术
作者
Candace B. Pert,Gavril W. Pasternak,Solomon H. Snyder
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1973-12-28
卷期号:182 (4119): 1359-1361
被引量:538
标识
DOI:10.1126/science.182.4119.1359
摘要
Receptor binding of opiate agonists and antagonists can be differentiated in vivo and in vitro. Administration of either rapidly elevates stereospecific [ 3 H]dihydromorphine binding to mouse brain extracts by 40 to 100 percent, but antagonists are 10 to 1000 times more potent than agonists; as little as 0.02 milligram of naloxone per kilogram of body weight significantly enhances opiate receptor binding. Sodium enhances antagonist binding in vitro but decreases agonist binding, a qualitative difference that may be relevant to the divergent pharmacological properties of opiate agonists and antagonists.
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