University of Michigan Medical School, Department of Pharmacology, 1150 W Medical Center Dr, Ann Arbor, MI 48109, USA.
University of Michigan Medical School, Department of Pharmacology, 1150 W Medical Center Dr, Ann Arbor, MI 48109, USA.
Behav Brain Res. 2020 Jul 15;390:112631. doi: 10.1016/j.bbr.2020.112631. Epub 2020 May 8.
Ketamine induces safe and effective anesthesia and displays unusual cataleptic properties that gave rise to the term dissociative anesthesia. Since 1970, clinicians only utilized the drug as an anesthetic or analgesic for decades, but ketamine was found to have rapid acting antidepressant effects in 1990s. Accumulated evidence exhibits NMDAR antagonism may not be the only mechanism of ketamine. The contributions of AMPA receptor, mTor signal pathway, monoaminergic system, sigma-1 receptor, cholinergic, opioid and cannabinoid systems, as well as voltage-gated calcium channels and hyperpolarization cyclic nucleotide gated channels are discussed for the antidepressant effects. Also the effects of ketamine's enantiomers and metabolites are reviewed. Furthermore ketamine's anesthetic and analgesic mechanisms are briefly revisited. Overall, pharmacology of ketamine, its enantiomers and metabolites is very unique. Insight into multiple mechanisms of action will provide further development and desirable clinical effects of ketamine.
氯胺酮诱导安全有效的麻醉,并表现出异常的镇静作用,这使得它被称为分离麻醉。自 1970 年以来,临床医生仅将该药物用作麻醉剂或镇痛药数十年,但在 20 世纪 90 年代发现氯胺酮具有快速抗抑郁作用。越来越多的证据表明,NMDA 受体拮抗作用可能不是氯胺酮的唯一作用机制。氯胺酮的 AMPA 受体、mTor 信号通路、单胺能系统、sigma-1 受体、胆碱能、阿片类和大麻素系统以及电压门控钙通道和超极化环核苷酸门控通道的作用都被认为与抗抑郁作用有关。此外,还综述了氯胺酮对映异构体和代谢物的作用。此外,还简要回顾了氯胺酮的麻醉和镇痛机制。总的来说,氯胺酮及其对映异构体和代谢物的药理学非常独特。对多种作用机制的深入了解将为氯胺酮的进一步发展和理想的临床效果提供帮助。