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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PubMed
Published
2025-04-25
DOI
https://doi.org/10.12116/j.issn.1004-5619.2024.341002
Primary Topic
Treatment of Major Depression
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article
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article

Molecular Mechanisms and Toxic Effects of Ketamine.

Jianbo Zhang, Yunxing Zuo, Tao Li, Wei Han
PubMed
Treatment of Major Depression
article

Molecular Mechanisms and Toxic Effects of Ketamine.

Jianbo Zhang, Yunxing Zuo, Tao Li, Wei Han
article en

Abstract

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.

PubMedVol. 41(2)
Xi'an Jiaotong University (CN)
Openalex Percentile: Top 77%
Treatment of Major Depression
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Molecular Mechanisms and Toxic Effects of Ketamine. — Jianbo Zhang, Yunxing Zuo, et al. · PubMed (2025) | TGRS Research Map | TGRS