• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

铁死亡与代谢综合征及其并发症:关联、机制与转化应用。

Ferroptosis and metabolic syndrome and complications: association, mechanism, and translational applications.

机构信息

Department of Endocrinology, Geriatric Endocrinology and Metabolism, Guangxi Key Laboratory of Precision Medicine in Cardio-Cerebrovascular Diseases Control and Prevention, Guangxi Clinical Research Center for Cardio-Cerebrovascular Diseases, First Affiliated Hospital, Guangxi Medical University, Nanning, China.

School of Nursing, Hunan University of Medicine, Huaihua, China.

出版信息

Front Endocrinol (Lausanne). 2024 Jan 8;14:1248934. doi: 10.3389/fendo.2023.1248934. eCollection 2023.

DOI:10.3389/fendo.2023.1248934
PMID:38260171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10800994/
Abstract

Metabolic syndrome is a medical condition characterized by several metabolic disorders in the body. Long-term metabolic disorders raise the risk of cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM). Therefore, it is essential to actively explore the aetiology of metabolic syndrome (MetS) and its comorbidities to provide effective treatment options. Ferroptosis is a new form of cell death that is characterized by iron overload, lipid peroxide accumulation, and decreased glutathione peroxidase 4(GPX4) activity, and it involves the pathological processes of a variety of diseases. Lipid deposition caused by lipid diseases and iron overload is significant in metabolic syndrome, providing the theoretical conditions for developing ferroptosis. Recent studies have found that the major molecules of ferroptosis are linked to common metabolic syndrome consequences, such as T2DM and atherosclerosis. In this review, we first discussed the mechanics of ferroptosis, the regulatory function of inducers and inhibitors of ferroptosis, and the significance of iron loading in MetS. Next, we summarized the role of ferroptosis in the pathogenesis of MetS, such as obesity, type 2 diabetes, and atherosclerosis. Finally, we discussed relevant ferroptosis-targeted therapies and raised some crucial issues of concern to provide directions for future Mets-related treatments and research.

摘要

代谢综合征是一种以体内多种代谢紊乱为特征的医学病症。长期的代谢紊乱会增加心血管疾病(CVD)和 2 型糖尿病(T2DM)的风险。因此,积极探索代谢综合征(MetS)及其合并症的病因,为提供有效的治疗方法至关重要。铁死亡是一种新的细胞死亡形式,其特征是铁过载、脂质过氧化物积累和谷胱甘肽过氧化物酶 4(GPX4)活性降低,涉及多种疾病的病理过程。脂质疾病和铁过载引起的脂质沉积在代谢综合征中很明显,为铁死亡的发展提供了理论条件。最近的研究发现,铁死亡的主要分子与常见的代谢综合征后果(如 2 型糖尿病和动脉粥样硬化)有关。在这篇综述中,我们首先讨论了铁死亡的机制、铁死亡诱导剂和抑制剂的调节功能以及 MetS 中铁超载的意义。接下来,我们总结了铁死亡在代谢综合征发病机制中的作用,如肥胖、2 型糖尿病和动脉粥样硬化。最后,我们讨论了相关的铁死亡靶向治疗,并提出了一些值得关注的关键问题,为未来的代谢综合征相关治疗和研究提供了方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/d36707a07d4e/fendo-14-1248934-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/c35ce9f6aafd/fendo-14-1248934-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/22ffe1a6b3de/fendo-14-1248934-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/5b39b0286867/fendo-14-1248934-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/d36707a07d4e/fendo-14-1248934-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/c35ce9f6aafd/fendo-14-1248934-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/22ffe1a6b3de/fendo-14-1248934-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/5b39b0286867/fendo-14-1248934-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa2/10800994/d36707a07d4e/fendo-14-1248934-g004.jpg

相似文献

1
Ferroptosis and metabolic syndrome and complications: association, mechanism, and translational applications.铁死亡与代谢综合征及其并发症:关联、机制与转化应用。
Front Endocrinol (Lausanne). 2024 Jan 8;14:1248934. doi: 10.3389/fendo.2023.1248934. eCollection 2023.
2
Mechanism of Ferroptosis and Its Role in Type 2 Diabetes Mellitus.铁死亡的机制及其在2型糖尿病中的作用
J Diabetes Res. 2021 Jun 28;2021:9999612. doi: 10.1155/2021/9999612. eCollection 2021.
3
Iron overload induces islet β cell ferroptosis by activating ASK1/P-P38/CHOP signaling pathway.铁过载通过激活 ASK1/P-P38/CHOP 信号通路诱导胰岛 β 细胞铁死亡。
PeerJ. 2023 Apr 18;11:e15206. doi: 10.7717/peerj.15206. eCollection 2023.
4
Mechanisms and regulations of ferroptosis.铁死亡的机制和调控。
Front Immunol. 2023 Oct 6;14:1269451. doi: 10.3389/fimmu.2023.1269451. eCollection 2023.
5
Ferroptosis in life: To be or not to be.铁死亡与生命:存在还是不存在。
Biomed Pharmacother. 2023 Mar;159:114241. doi: 10.1016/j.biopha.2023.114241. Epub 2023 Jan 10.
6
Erythropoietin ameliorates cognitive dysfunction in mice with type 2 diabetes mellitus via inhibiting iron overload and ferroptosis.促红细胞生成素通过抑制铁过载和铁死亡改善 2 型糖尿病小鼠的认知功能障碍。
Exp Neurol. 2023 Jul;365:114414. doi: 10.1016/j.expneurol.2023.114414. Epub 2023 Apr 17.
7
The mechanisms of ferroptosis and its role in atherosclerosis.铁死亡的机制及其在动脉粥样硬化中的作用。
Biomed Pharmacother. 2024 Feb;171:116112. doi: 10.1016/j.biopha.2023.116112. Epub 2024 Jan 2.
8
Vitamin D May Play a Vital Role in Alleviating Type 2 Diabetes Mellitus by Modulating the Ferroptosis Signaling Pathway.维生素 D 通过调节铁死亡信号通路可能在缓解 2 型糖尿病中发挥重要作用。
Horm Metab Res. 2024 Mar;56(3):193-196. doi: 10.1055/a-2122-5701. Epub 2023 Jul 4.
9
Dysmetabolic Iron Overload in Metabolic Syndrome.代谢综合征中的代谢性铁过载。
Curr Pharm Des. 2020;26(10):1019-1024. doi: 10.2174/1381612826666200130090703.
10
Iron metabolism and ferroptosis in type 2 diabetes mellitus and complications: mechanisms and therapeutic opportunities.2 型糖尿病及其并发症中铁代谢与铁死亡:机制与治疗机遇。
Cell Death Dis. 2023 Mar 8;14(3):186. doi: 10.1038/s41419-023-05708-0.

引用本文的文献

1
Targeting ferroptosis for neuroprotection: potential therapeutic avenues in neurodegenerative and neuropsychiatric diseases.靶向铁死亡进行神经保护:神经退行性疾病和神经精神疾病的潜在治疗途径
Front Physiol. 2025 Aug 28;16:1641323. doi: 10.3389/fphys.2025.1641323. eCollection 2025.
2
Life-threatening risk factors contribute to the development of diseases with the highest mortality through the induction of regulated necrotic cell death.危及生命的风险因素通过诱导程序性坏死性细胞死亡,促成了死亡率最高的疾病的发展。
Cell Death Dis. 2025 Apr 11;16(1):273. doi: 10.1038/s41419-025-07563-7.
3
Ferroptosis: mechanism and role in diabetes-related cardiovascular diseases.

本文引用的文献

1
Ferroptosis, a new pathogenetic mechanism in cardiometabolic diseases and cancer: Is there a role for statin therapy?铁死亡,一种在心脏代谢疾病和癌症中的新发病机制:他汀类药物治疗是否有作用?
Metabolism. 2023 Sep;146:155659. doi: 10.1016/j.metabol.2023.155659. Epub 2023 Jul 11.
2
Ferroptosis surveillance independent of GPX4 and differentially regulated by sex hormones.铁死亡监测不依赖于 GPX4 且受性激素差异调控。
Cell. 2023 Jun 22;186(13):2748-2764.e22. doi: 10.1016/j.cell.2023.05.003. Epub 2023 Jun 1.
3
1,25D/VDR inhibits pancreatic β cell ferroptosis by downregulating FOXO1 expression in diabetes mellitus.
铁死亡:在糖尿病相关心血管疾病中的机制及作用
Cardiovasc Diabetol. 2025 Feb 7;24(1):60. doi: 10.1186/s12933-025-02614-x.
4
Ferroptosis, a therapeutic target for cardiovascular diseases, neurodegenerative diseases and cancer.铁死亡,一种针对心血管疾病、神经退行性疾病和癌症的治疗靶点。
J Transl Med. 2024 Dec 22;22(1):1137. doi: 10.1186/s12967-024-05881-6.
5
Insulin Resistance, Hyperinsulinemia and Atherosclerosis: Insights into Pathophysiological Aspects and Future Therapeutic Prospects.胰岛素抵抗、高胰岛素血症与动脉粥样硬化:对病理生理方面及未来治疗前景的见解
Curr Cardiol Rev. 2025;21(1):e1573403X314035. doi: 10.2174/011573403X314035241006185109.
6
Biomarkers That Seem to Have the Greatest Impact on Promoting the Formation of Atherosclerotic Plaque in Current Scientific Research.在当前科学研究中似乎对促进动脉粥样硬化斑块形成影响最大的生物标志物。
Curr Issues Mol Biol. 2024 Aug 29;46(9):9503-9522. doi: 10.3390/cimb46090564.
7
The herbicide acetochlor causes lipid peroxidation by inhibition of glutathione peroxidase activity.除草剂乙草胺通过抑制谷胱甘肽过氧化物酶活性引起脂质过氧化。
Toxicol Sci. 2024 Dec 1;202(2):302-313. doi: 10.1093/toxsci/kfae113.
8
Red Oranges and Olive Leaf Waste-Derived Bioactive Extracts Promote Adipocyte Functionality In Vitro.红橙和橄榄叶废料衍生的生物活性提取物可促进体外脂肪细胞功能。
Nutrients. 2024 Jun 19;16(12):1959. doi: 10.3390/nu16121959.
9
Hazel Leaf Polyphenol Extract Alleviated Cisplatin-Induced Acute Kidney Injury by Reducing Ferroptosis through Inhibiting Hippo Signaling.榛叶多酚提取物通过抑制Hippo信号通路减少铁死亡,减轻顺铂诱导的急性肾损伤。
Molecules. 2024 Apr 11;29(8):1729. doi: 10.3390/molecules29081729.
1,25D/VDR 通过下调糖尿病中 FOXO1 的表达抑制胰腺 β 细胞铁死亡。
Cell Signal. 2023 May;105:110564. doi: 10.1016/j.cellsig.2022.110564. Epub 2022 Dec 26.
4
Upregulation of Nrf2 Signalling and the Inhibition of Erastin-Induced Ferroptosis by Ferulic Acid in MIN6 Cells.阿魏酸通过上调 Nrf2 信号通路抑制 MIN6 细胞中 Erastin 诱导的铁死亡。
Int J Mol Sci. 2022 Dec 14;23(24):15886. doi: 10.3390/ijms232415886.
5
Oleoylethanolamide alleviates hyperlipidaemia-mediated vascular calcification via attenuating mitochondrial DNA stress triggered autophagy-dependent ferroptosis by activating PPARα.油酰乙醇酰胺通过激活 PPARα 减轻线粒体 DNA 应激引发的自噬依赖性铁死亡来缓解高脂血症介导的血管钙化。
Biochem Pharmacol. 2023 Feb;208:115379. doi: 10.1016/j.bcp.2022.115379. Epub 2022 Dec 13.
6
RAGE promotes dysregulation of iron and lipid metabolism in alcoholic liver disease.RAGE 促进酒精性肝病中铁和脂质代谢的失调。
Redox Biol. 2023 Feb;59:102559. doi: 10.1016/j.redox.2022.102559. Epub 2022 Dec 1.
7
Ferroptosis increases obesity: Crosstalk between adipocytes and the neuroimmune system.铁死亡增加肥胖:脂肪细胞与神经免疫系统的串扰。
Front Immunol. 2022 Nov 21;13:1049936. doi: 10.3389/fimmu.2022.1049936. eCollection 2022.
8
Berberine Regulates GPX4 to Inhibit Ferroptosis of Islet β Cells.小檗碱通过调控 GPX4 抑制胰岛β细胞铁死亡。
Planta Med. 2023 Mar;89(3):254-261. doi: 10.1055/a-1939-7417. Epub 2022 Nov 9.
9
IDH1 Promotes Foam Cell Formation by Aggravating Macrophage Ferroptosis.异柠檬酸脱氢酶1通过加剧巨噬细胞铁死亡促进泡沫细胞形成。
Biology (Basel). 2022 Sep 23;11(10):1392. doi: 10.3390/biology11101392.
10
Qing-Xin-Jie-Yu Granule inhibits ferroptosis and stabilizes atherosclerotic plaques by regulating the GPX4/xCT signaling pathway.清心安瘀颗粒通过调节 GPX4/xCT 信号通路抑制铁死亡稳定动脉粥样硬化斑块。
J Ethnopharmacol. 2023 Jan 30;301:115852. doi: 10.1016/j.jep.2022.115852. Epub 2022 Oct 20.