Zhou Liang, Duan Jingjing
Department of Pharmacology, College of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Department of Anatomy and Neurobiology, Zhongshan School of Medicine, SunYat-sen University, Guangzhou, China.
CNS Neurosci Ther. 2024 Apr;30(4):e14464. doi: 10.1111/cns.14464. Epub 2023 Sep 7.
As a phencyclidine (PCP) analog, ketamine can generate rapid-onset and substantial anesthetic effects. Contrary to traditional anesthetics, ketamine is a dissociative anesthetic and can induce loss of consciousness in patients. Recently, the subanaesthetic dose of ketamine was found to produce rapid-onset and lasting antidepressant effects.
However, how different concentrations of ketamine can induce diverse actions remains unclear. Furthermore, the molecular mechanisms underlying the NMDAR-mediated anesthetic and antidepressant effects of ketamine are not fully understood.
In this review, we have introduced ketamine and its metabolism, summarized recent advances in the molecular mechanisms underlying NMDAR inhibition in the anesthetic and antidepressant effects of ketamine, explored the possible functions of NMDAR subunits in the effects of ketamine, and discussed the future directions of ketamine-based anesthetic and antidepressant drugs.
Both the anesthetic and antidepressant effects of ketamine were thought to be mediated by N-methyl-D-aspartate receptor (NMDAR) inhibition.
The roles of NMDARs have been extensively studied in the anaesthetic effects of ketamine. However, the roles of NMDARs in antidepressant effects of ketamine are complicated and controversial.
作为苯环己哌啶(PCP)类似物,氯胺酮可产生快速起效且显著的麻醉作用。与传统麻醉药不同,氯胺酮是一种解离性麻醉药,可导致患者意识丧失。最近发现,亚麻醉剂量的氯胺酮能产生快速起效且持久的抗抑郁作用。
然而,不同浓度的氯胺酮如何诱导不同作用仍不清楚。此外,氯胺酮N-甲基-D-天冬氨酸受体(NMDAR)介导的麻醉和抗抑郁作用的分子机制尚未完全阐明。
在本综述中,我们介绍了氯胺酮及其代谢,总结了氯胺酮麻醉和抗抑郁作用中NMDAR抑制的分子机制的最新进展,探讨了NMDAR亚基在氯胺酮作用中的可能功能,并讨论了基于氯胺酮的麻醉和抗抑郁药物的未来方向。
氯胺酮的麻醉和抗抑郁作用均被认为是由N-甲基-D-天冬氨酸受体(NMDAR)抑制介导的。
NMDAR在氯胺酮麻醉作用中的作用已得到广泛研究。然而,NMDAR在氯胺酮抗抑郁作用中的作用复杂且存在争议。