Zhou Jian-Shun, Peng Guan-Fa, Liang Wei-Dong, Chen Zhen, Liu Ying-Ying, Wang Bing-Yu, Guo Ming-Ling, Deng Yun-Ling, Ye Jun-Ming, Zhong Mao-Lin, Wang Li-Feng
The First Clinical Medical College of Gannan Medical University, Ganzhou, China.
Department of Anesthesiology, First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
Front Pharmacol. 2023 Sep 14;14:1228895. doi: 10.3389/fphar.2023.1228895. eCollection 2023.
Ketamine is a racemic mixture of equal amounts of R-ketamine and S-ketamine and is well known to anesthesiologists for its unique dissociative anesthetic properties. The pharmacological properties of ketamine, namely, its sympathetic excitation, mild respiratory depression, and potent analgesia, are still highly valued in its use as an anesthetic for some patients. In particular, since its advent, S-ketamine has been widely used as an anesthetic in many countries due to its increased affinity for NMDA receptors and its enhanced anesthetic and analgesic effects. However, the anesthetic and analgesic mechanisms of S-ketamine are not fully understood. In addition to antagonizing NMDA receptors, a variety of other receptors or channels may be involved, but there are no relevant mechanistic summaries in the literature. Therefore, the purpose of this paper is to review the mechanisms of action of S-ketamine on relevant receptors and systems in the body that result in its pharmacological properties, such as anesthesia and analgesia, with the aim of providing a reference for its clinical applications and research.
氯胺酮是等量R-氯胺酮和S-氯胺酮的外消旋混合物,因其独特的解离麻醉特性而被麻醉医生所熟知。氯胺酮的药理特性,即其交感神经兴奋、轻度呼吸抑制和强效镇痛作用,在其作为某些患者的麻醉剂使用中仍然备受重视。特别是,自问世以来,S-氯胺酮因其对NMDA受体的亲和力增加以及增强的麻醉和镇痛效果,已在许多国家被广泛用作麻醉剂。然而,S-氯胺酮的麻醉和镇痛机制尚未完全明确。除了拮抗NMDA受体外,可能还涉及多种其他受体或通道,但文献中尚无相关的机制总结。因此,本文旨在综述S-氯胺酮对体内相关受体和系统的作用机制,这些机制导致了其药理特性,如麻醉和镇痛,以期为其临床应用和研究提供参考。