氯胺酮的分子机制和毒性作用。

Q3 Medicine
Yu-Meng Zuo, Wei Han, Jian-Bo Zhang, Tao Li
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引用次数: 0

摘要

氯胺酮是一种游离性麻醉剂。临床上用作手术麻醉剂或麻醉诱导剂,有一定的精神依赖性。它的滥用会导致神经损伤、不良情绪反应和其他有毒副作用。氯胺酮发挥药理作用的主要机制是阻断n -甲基- d -天冬氨酸受体(NMDAR)。它还通过α-氨基-3-羟基-5-甲基-4-异氧-唑烯丙酸受体(AMPAR)、阿片受体、γ-氨基丁酸(GABA)受体、单胺能受体、胆碱能受体、超极化激活环核苷酸门控(HCN)通道、电压门控钠通道和l型电压依赖性钙通道(VDCC)等途径发挥作用。本文就氯胺酮药理作用的分子机制和毒性作用进行综述,以期为氯胺酮毒性作用的症状表型鉴定和氯胺酮滥用鉴定等法医应用提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Mechanisms and Toxic Effects of Ketamine.

Ketamine is a dissociative anesthetic. It is clinically used as a surgical anesthetic or anesthetic inducer and has a certain degree of mental dependence. Its abuse can lead to nerve damage, adverse emotional reactions and other toxic side effects. The primary mechanism by which ketamine exerts its pharmacological effects is to block N-methyl-D-aspartate receptors (NMDAR). It also functions through pathways such as α-amino-3-hydroxy-5-methyl-4-isox-azolepropionic acid receptors (AMPAR), opioid receptors, γ-aminobutyric acid (GABA) receptors, monoaminergic receptors, cholinergic receptors, hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, voltage-gated sodium channels, and L-type voltage-dependent calcium channels (VDCC). This article summarizes the molecular mechanism and toxic effects of ketamine's pharmacological functions, in order to provide a basis for forensic applications such as the identification of symptomatic phenotypes of ketamine toxic effects and the identification of ketamine abuse.

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来源期刊
法医学杂志
法医学杂志 Medicine-Pathology and Forensic Medicine
CiteScore
1.50
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