Taipei Medical University-Wan Fang Hospital, Department of Anesthesiology, Taipei, Taiwan.
Expert Opin Drug Metab Toxicol. 2010 Mar;6(3):273-81. doi: 10.1517/17425250903505108.
Ketamine, a widely used intravenous anesthetic agent, is biotransformed by cytochrome P450s (CYPs). Considerable attention is devoted to the ketamine-involved regulation of CYP gene expression. Assessing how ketamine regulates CYP gene expression is significant in recognizing the pharmacology of this anesthetic agent and its clinical application.
In this review, the authors discuss the effects of ketamine on the regulation of CYP gene expression and its possible mechanisms from the aspects of cytoskeletal remodeling, mitochondrial dysfunction, and alterations of intracellular ATP levels and calcium homeostasis.
This review may provide readers with more clues for recognizing and avoiding possible ketamine-drug interactions.
Ketamine may inhibit CYP3A4 expression possibly through reducing calcium mobilization and mitochondrial ATP synthesis and consequently disturbing cytoskeleton remodeling.
氯胺酮,一种广泛使用的静脉麻醉剂,由细胞色素 P450 (CYPs)生物转化。相当多的注意力都集中在涉及氯胺酮的 CYP 基因表达调控上。评估氯胺酮如何调节 CYP 基因表达对于认识这种麻醉剂的药理学及其临床应用具有重要意义。
在这篇综述中,作者从细胞骨架重塑、线粒体功能障碍以及细胞内 ATP 水平和钙稳态的改变等方面讨论了氯胺酮对 CYP 基因表达调控的影响及其可能的机制。
本综述可能为读者提供更多线索,以识别和避免可能的氯胺酮-药物相互作用。
氯胺酮可能通过减少钙动员和线粒体 ATP 合成,从而干扰细胞骨架重塑,抑制 CYP3A4 的表达。