氯胺酮
NMDA受体
药理学
离解的
类阿片
止痛药
抗抑郁药
阿片受体
作用机理
医学
焦虑
受体
麻醉
化学
精神科
内科学
体外
生物化学
作者
Marjorie R. Levinstein,Reece C. Budinich,Jordi Bonaventura,Alan F. Schatzberg,Carlos A. Zarate,Michel Michaelides
标识
DOI:10.1176/appi.ajp.20240378
摘要
-methyl-d-aspartate (NMDA) receptor antagonist. In this review, the authors argue that ketamine's pharmacology should be redefined to include opioid receptors and the endogenous opioid system. They also highlight a potential mechanism of action of ketamine for depression that is attributed to bifunctional, synergistic interactions involving NMDA and opioid receptors.
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