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铁死亡对心血管疾病的影响。

Effects of Ferroptosis on Cardiovascular Diseases.

机构信息

Core Facilities, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.

出版信息

Mediators Inflamm. 2023 May 4;2023:6653202. doi: 10.1155/2023/6653202. eCollection 2023.

DOI:10.1155/2023/6653202
PMID:37181809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10175025/
Abstract

Ferroptosis is a novel form of programmed cell death characterized by the accumulation of iron-dependent lipid peroxides, which causes membrane injury. Under the catalysis of iron ions, cells deficient in glutathione peroxidase (GPX4) cannot preserve the balance in lipid oxidative metabolism, and the buildup of reactive oxygen species on the membrane lipids leads to cell death. An increasing body of evidence suggests that ferroptosis plays a significant role in the development and occurrence of cardiovascular diseases. In this paper, we mainly elaborated on the molecular mechanisms regulating ferroptosis and its impact on cardiovascular disease to lay the groundwork for future studies on the prophylaxis and treatment of this patient population.

摘要

铁死亡是一种新型的程序性细胞死亡方式,其特征是铁依赖性脂质过氧化物的积累,导致膜损伤。在铁离子的催化作用下,谷胱甘肽过氧化物酶 (GPX4) 缺乏的细胞无法维持脂质氧化代谢的平衡,膜脂质上活性氧的积累导致细胞死亡。越来越多的证据表明,铁死亡在心血管疾病的发展和发生中起着重要作用。本文主要阐述了调节铁死亡的分子机制及其对心血管疾病的影响,为研究该患者人群的预防和治疗奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27fd/10175025/5c7645389f2b/MI2023-6653202.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27fd/10175025/5c7645389f2b/MI2023-6653202.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27fd/10175025/5c7645389f2b/MI2023-6653202.001.jpg

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本文引用的文献

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The Beneficial Effects of Geniposide on Glucose and Lipid Metabolism: A Review.栀子苷对糖脂代谢的有益作用:综述。
Drug Des Devel Ther. 2022 Sep 30;16:3365-3383. doi: 10.2147/DDDT.S378976. eCollection 2022.
2
Gut microbiota profiling revealed the regulating effects of salidroside on iron metabolism in diabetic mice.肠道微生物组分析揭示了红景天苷对糖尿病小鼠铁代谢的调节作用。
Front Endocrinol (Lausanne). 2022 Sep 23;13:1014577. doi: 10.3389/fendo.2022.1014577. eCollection 2022.
3
Salidroside in the Treatment of NAFLD/NASH.红景天苷治疗非酒精性脂肪性肝病/非酒精性脂肪性肝炎。
Chem Biodivers. 2022 Dec;19(12):e202200401. doi: 10.1002/cbdv.202200401. Epub 2022 Nov 14.
4
Protective effects of Salvianolic acid B on rat ferroptosis in myocardial infarction through upregulating the Nrf2 signaling pathway.丹酚酸 B 通过上调 Nrf2 信号通路对心肌梗死大鼠铁死亡的保护作用。
Int Immunopharmacol. 2022 Nov;112:109257. doi: 10.1016/j.intimp.2022.109257. Epub 2022 Sep 26.
5
Astragaloside IV regulates the ferroptosis signaling pathway via the Nrf2/SLC7A11/GPX4 axis to inhibit PM2.5-mediated lung injury in mice.黄芪甲苷通过 Nrf2/SLC7A11/GPX4 轴调节铁死亡信号通路抑制 PM2.5 介导的小鼠肺损伤。
Int Immunopharmacol. 2022 Nov;112:109186. doi: 10.1016/j.intimp.2022.109186. Epub 2022 Sep 15.
6
New Deferric Amine Compounds Efficiently Chelate Excess Iron to Treat Iron Overload Disorders and to Prevent Ferroptosis.新型去铁胺化合物能有效螯合多余的铁,用于治疗铁过载疾病和预防铁死亡。
Adv Sci (Weinh). 2022 Oct;9(29):e2202679. doi: 10.1002/advs.202202679. Epub 2022 Aug 28.
7
Updated Pharmacological Effects, Molecular Mechanisms, and Therapeutic Potential of Natural Product Geniposide.天然产物京尼平苷的更新药理学作用、分子机制和治疗潜力。
Molecules. 2022 May 21;27(10):3319. doi: 10.3390/molecules27103319.
8
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Front Pharmacol. 2022 May 5;13:879870. doi: 10.3389/fphar.2022.879870. eCollection 2022.
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Front Nutr. 2022 Apr 25;9:865077. doi: 10.3389/fnut.2022.865077. eCollection 2022.
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Oxid Med Cell Longev. 2022 Apr 18;2022:9304383. doi: 10.1155/2022/9304383. eCollection 2022.