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麻醉药品对铁死亡相关分子机制和信号通路的影响。

The effect of narcotics on ferroptosis-related molecular mechanisms and signalling pathways.

作者信息

Zeng Xiaoqin, Li Jingda, Yang Fuyuan, Xia Rui

机构信息

Department of Anaesthesiology, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, China.

College of Life Sciences, Yangtze University, Jingzhou, Hubei, China.

出版信息

Front Pharmacol. 2022 Oct 13;13:1020447. doi: 10.3389/fphar.2022.1020447. eCollection 2022.

DOI:10.3389/fphar.2022.1020447
PMID:36313359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9606818/
Abstract

Ferroptosis is a novel programmed cell death form characterized by iron-mediated reactive oxygen species-induced lipid peroxidation and subsequent cell damage that is distinct from apoptosis, necroptosis, pyroptosis, and autophagy. Most studies on ferroptosis are based on its function and mechanism, but there have been relatively few studies on the effects of drugs, especially anaesthetics, on ferroptosis. Therefore, we summarized the recent literature on the effects of anaesthetics on ferroptosis to understand the underlying mechanism. In particular, we focused on the targets of various anaesthetics in different mechanisms of ferroptosis and the effects of ferroptosis induction or inhibition by narcotics on various diseases. The aims of this review are to provide a relatively reasonable drug regimen for clinicians, to explore potential ferroptosis protection drugs and targets, to reduce perioperative complications and to improve the postoperative performance of patients, especially those who are critically ill.

摘要

铁死亡是一种新型的程序性细胞死亡形式,其特征是铁介导的活性氧诱导的脂质过氧化以及随后的细胞损伤,这与凋亡、坏死性凋亡、焦亡和自噬不同。大多数关于铁死亡的研究基于其功能和机制,但关于药物,尤其是麻醉药对铁死亡影响的研究相对较少。因此,我们总结了近期关于麻醉药对铁死亡影响的文献,以了解其潜在机制。特别是,我们关注了各种麻醉药在铁死亡不同机制中的靶点,以及麻醉药诱导或抑制铁死亡对各种疾病的影响。本综述的目的是为临床医生提供相对合理的用药方案,探索潜在的铁死亡保护药物和靶点,减少围手术期并发症,改善患者,尤其是重症患者的术后表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/54ef79fdd0b6/fphar-13-1020447-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/a9def822edc9/fphar-13-1020447-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/e8ed623f0888/fphar-13-1020447-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/080ada48e60e/fphar-13-1020447-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/54ef79fdd0b6/fphar-13-1020447-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/a9def822edc9/fphar-13-1020447-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/e8ed623f0888/fphar-13-1020447-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/080ada48e60e/fphar-13-1020447-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3a/9606818/54ef79fdd0b6/fphar-13-1020447-g004.jpg

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本文引用的文献

1
Mitochondria-Related Ferroptosis Drives Cognitive Deficits in Neonatal Mice Following Sevoflurane Administration.线粒体相关的铁死亡驱动新生小鼠在七氟醚给药后出现认知缺陷。
Front Med (Lausanne). 2022 Jul 22;9:887062. doi: 10.3389/fmed.2022.887062. eCollection 2022.
2
Dexmedetomidine Attenuates Ferroptosis-Mediated Renal Ischemia/Reperfusion Injury and Inflammation by Inhibiting ACSL4 α2-AR.右美托咪定通过抑制ACSL4 α2-肾上腺素能受体减轻铁死亡介导的肾缺血/再灌注损伤和炎症反应。
Front Pharmacol. 2022 Jun 14;13:782466. doi: 10.3389/fphar.2022.782466. eCollection 2022.
3
Postoperative Cognitive Dysfunction and Alzheimer's Disease: A Transcriptome-Based Comparison of Animal Models.
铁死亡在麻醉药对多器官疾病影响中的作用:文献综述
Heliyon. 2023 Sep 23;9(10):e20405. doi: 10.1016/j.heliyon.2023.e20405. eCollection 2023 Oct.
术后认知功能障碍与阿尔茨海默病:基于转录组的动物模型比较
Front Aging Neurosci. 2022 Jun 28;14:900350. doi: 10.3389/fnagi.2022.900350. eCollection 2022.
4
Propofol Protects Against Erastin-Induced Ferroptosis in HT-22 Cells.丙泊酚可保护HT-22细胞免受艾拉司丁诱导的铁死亡。
J Mol Neurosci. 2022 Sep;72(9):1797-1808. doi: 10.1007/s12031-022-02017-7. Epub 2022 Jun 21.
5
Post-Translational Modifications of p53 in Ferroptosis: Novel Pharmacological Targets for Cancer Therapy.铁死亡中p53的翻译后修饰:癌症治疗的新型药理学靶点
Front Pharmacol. 2022 May 24;13:908772. doi: 10.3389/fphar.2022.908772. eCollection 2022.
6
Corrigendum: Propofol Protects Myocardium From Ischemia/Reperfusion Injury by Inhibiting Ferroptosis Through the AKT/p53 Signaling Pathway.勘误:丙泊酚通过AKT/p53信号通路抑制铁死亡从而保护心肌免受缺血/再灌注损伤。
Front Pharmacol. 2022 Apr 28;13:910421. doi: 10.3389/fphar.2022.910421. eCollection 2022.
7
Propofol Augments Paclitaxel-Induced Cervical Cancer Cell Ferroptosis .丙泊酚增强紫杉醇诱导的宫颈癌细胞铁死亡
Front Pharmacol. 2022 Apr 20;13:816432. doi: 10.3389/fphar.2022.816432. eCollection 2022.
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Research Progress of Ferroptosis in Adiposity-Based Chronic Disease (ABCD).基于肥胖的慢性疾病(ABCD)中铁死亡的研究进展。
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Sevoflurane Induces Ferroptosis of Glioma Cells Through Activating the ATF4-CHAC1 Pathway.七氟醚通过激活ATF4-CHAC1信号通路诱导胶质瘤细胞铁死亡
Front Oncol. 2022 Mar 17;12:859621. doi: 10.3389/fonc.2022.859621. eCollection 2022.