• 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

靶向铁死亡干预糖尿病性心肌病的潜在意义

Potential Significance of Targeting Ferroptosis for Intervention of Diabetic Cardiomyopathy.

作者信息

Lei Qian, Yang Burton B, Lyu Juanjuan

机构信息

Anesthesia and Operation Center, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.

School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

出版信息

J Diabetes. 2025 Jun;17(6):e70116. doi: 10.1111/1753-0407.70116.

DOI:10.1111/1753-0407.70116
PMID:40536196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12177803/
Abstract

BACKGROUND

Diabetes represents a significant global health concern, with diabetic cardiomyopathy (DCM) emerging as a primary cause of mortality among individuals with diabetes. Despite the prevalence of DCM, advancements in therapeutic and preventative strategies remain constrained.

METHODS

Recent studies were reviewed to provide a comprehensive summary of pathogenesis and clinical treatment of DCM, effect of ferroptosis, and potential value of ferroptosis inhibitors in DCM intervention.

RESULTS

A growing body of research indicates that oxidative stress, inflammatory reactions, and other factors play a role in the onset and progression of DCM. Oxidative stress within cardiomyocytes is a primary mechanism implicated in the development of DCM, whereby heightened intracellular reactive oxygen species (ROS) facilitate cell death via ferroptosis. Ferroptosis inhibitors hold great promise as therapeutic agents.

CONCLUSIONS

This review provides an overview of the involvement of iron homeostasis regulation, oxidative stress, and ferroptosis in DCM, and the significance of ferroptosis in the prevention and treatment of DCM.

摘要

背景

糖尿病是一个重大的全球健康问题,糖尿病性心肌病(DCM)已成为糖尿病患者死亡的主要原因。尽管DCM很普遍,但治疗和预防策略的进展仍然有限。

方法

回顾近期研究,以全面总结DCM的发病机制和临床治疗、铁死亡的作用以及铁死亡抑制剂在DCM干预中的潜在价值。

结果

越来越多的研究表明,氧化应激、炎症反应和其他因素在DCM的发生和发展中起作用。心肌细胞内的氧化应激是DCM发生的主要机制,细胞内活性氧(ROS)水平升高通过铁死亡促进细胞死亡。铁死亡抑制剂作为治疗药物具有很大的潜力。

结论

本综述概述了铁稳态调节、氧化应激和铁死亡在DCM中的作用,以及铁死亡在DCM预防和治疗中的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8907/12177803/c289ed5b6355/JDB-17-e70116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8907/12177803/9681374f6ce3/JDB-17-e70116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8907/12177803/c289ed5b6355/JDB-17-e70116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8907/12177803/9681374f6ce3/JDB-17-e70116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8907/12177803/c289ed5b6355/JDB-17-e70116-g003.jpg

相似文献

1
Potential Significance of Targeting Ferroptosis for Intervention of Diabetic Cardiomyopathy.靶向铁死亡干预糖尿病性心肌病的潜在意义
J Diabetes. 2025 Jun;17(6):e70116. doi: 10.1111/1753-0407.70116.
2
Ferroptosis in diabetic cardiomyopathy: from its mechanisms to therapeutic strategies.糖尿病性心肌病中的铁死亡:从机制到治疗策略。
Front Endocrinol (Lausanne). 2024 Nov 11;15:1421838. doi: 10.3389/fendo.2024.1421838. eCollection 2024.
3
Irisin Protects Against Diabetic Cardiomyopathy by Suppressing Ferroptosis.鸢尾素通过抑制铁死亡来预防糖尿病性心肌病。
Drug Dev Res. 2025 Jun;86(4):e70077. doi: 10.1002/ddr.70077.
4
New insights into FGF21 alleviates diabetic cardiomyopathy by suppressing ferroptosis: a commentary.成纤维细胞生长因子 21 通过抑制铁死亡缓解糖尿病心肌病的新见解:述评。
Cardiovasc Diabetol. 2024 Nov 26;23(1):424. doi: 10.1186/s12933-024-02519-1.
5
[Ferroptosis-related long non-coding RNA to predict the clinical outcome of non-small cell lung cancer after radiotherapy].[铁死亡相关长链非编码RNA预测非小细胞肺癌放疗后的临床结局]
Beijing Da Xue Xue Bao Yi Xue Ban. 2025 Jun 18;57(3):569-577. doi: 10.19723/j.issn.1671-167X.2025.03.022.
6
Perillaldehyde synergizes with ferroptosis inducers to promote ferroptotic cell death in gastric cancer.紫苏醛与铁死亡诱导剂协同作用,促进胃癌细胞的铁死亡。
Front Cell Dev Biol. 2025 Jun 3;13:1598520. doi: 10.3389/fcell.2025.1598520. eCollection 2025.
7
Trapidil attenuates diabetic cardiomyopathy via GPX3/Nrf2-mediated inhibition of myocardial pyroptosis.曲匹地尔通过GPX3/Nrf2介导的对心肌细胞焦亡的抑制作用减轻糖尿病心肌病。
Front Pharmacol. 2025 Jun 3;16:1566622. doi: 10.3389/fphar.2025.1566622. eCollection 2025.
8
Ferroptosis as a potential molecular mechanism of bipolar disorder.铁死亡作为双相情感障碍的一种潜在分子机制。
Transl Psychiatry. 2025 Jun 19;15(1):205. doi: 10.1038/s41398-025-03429-w.
9
Fibroblast growth factor 21 improves diabetic cardiomyopathy by inhibiting ferroptosis via ferritin pathway.成纤维细胞生长因子 21 通过铁蛋白途径抑制铁死亡改善糖尿病心肌病。
Cardiovasc Diabetol. 2024 Nov 2;23(1):394. doi: 10.1186/s12933-024-02469-8.
10
MiR214-3p Ameliorates Diabetic Cardiomyopathy by Inhibiting Ferroptosis.MiR214-3p通过抑制铁死亡改善糖尿病心肌病。
Cardiovasc Toxicol. 2025 Jun;25(6):884-897. doi: 10.1007/s12012-025-09992-4. Epub 2025 Apr 7.

引用本文的文献

1
METTL14 Hinders DCM Progression via Mediating the m6A Methylation of NRG4 in HG-Induced H9C2 Cells.METTL14通过介导高糖诱导的H9C2细胞中NRG4的m6A甲基化来抑制扩张型心肌病进展。
Mol Biotechnol. 2025 Sep 2. doi: 10.1007/s12033-025-01507-4.

本文引用的文献

1
Phospholipids with two polyunsaturated fatty acyl tails promote ferroptosis.带有两条多不饱和脂肪酰基尾巴的磷脂会促进铁死亡。
Cell. 2024 Feb 29;187(5):1177-1190.e18. doi: 10.1016/j.cell.2024.01.030. Epub 2024 Feb 15.
2
Paeoniflorin confers ferroptosis resistance by regulating the gut microbiota and its metabolites in diabetic cardiomyopathy.芍药苷通过调节糖尿病心肌病中的肠道微生物群及其代谢物发挥铁死亡抵抗作用。
Am J Physiol Cell Physiol. 2024 Mar 1;326(3):C724-C741. doi: 10.1152/ajpcell.00565.2023. Epub 2024 Jan 15.
3
Nicorandil alleviates cardiac microvascular ferroptosis in diabetic cardiomyopathy: Role of the mitochondria-localized AMPK-Parkin-ACSL4 signaling pathway.
尼可地尔减轻糖尿病心肌病中的心脏微血管铁死亡:线粒体定位的AMPK-Parkin-ACSL4信号通路的作用
Pharmacol Res. 2024 Feb;200:107057. doi: 10.1016/j.phrs.2024.107057. Epub 2024 Jan 11.
4
Ferroptosis in cardiovascular disease.铁死亡与心血管疾病
Biomed Pharmacother. 2024 Jan;170:116057. doi: 10.1016/j.biopha.2023.116057. Epub 2023 Dec 29.
5
Upregulation of NF-κB by USP24 aggravates ferroptosis in diabetic cardiomyopathy.USP24 通过上调 NF-κB 加重糖尿病心肌病中的铁死亡。
Free Radic Biol Med. 2024 Jan;210:352-366. doi: 10.1016/j.freeradbiomed.2023.11.032. Epub 2023 Dec 5.
6
Lipid-lowering in diabetes: An update.糖尿病患者的降脂治疗:最新进展。
Atherosclerosis. 2024 Jul;394:117313. doi: 10.1016/j.atherosclerosis.2023.117313. Epub 2023 Oct 6.
7
Inhibition of fatty acid oxidation enables heart regeneration in adult mice.脂肪酸氧化抑制可促进成年小鼠的心脏再生。
Nature. 2023 Oct;622(7983):619-626. doi: 10.1038/s41586-023-06585-5. Epub 2023 Sep 27.
8
Suberosin Alleviates Thiazolidinedione-Induced Cardiomyopathy in Diabetic Rats by Inhibiting Ferroptosis via Modulation of ACSL4-LPCAT3 and PI3K-AKT Signaling Pathways.亚油酸酰胺通过调节 ACSL4-LPCAT3 和 PI3K-AKT 信号通路抑制铁死亡缓解噻唑烷二酮诱导的糖尿病大鼠心肌病。
Cardiovasc Toxicol. 2023 Oct;23(9-10):295-304. doi: 10.1007/s12012-023-09804-7. Epub 2023 Sep 7.
9
What is the impact of ferroptosis on diabetic cardiomyopathy: a systematic review.铁死亡对糖尿病性心肌病的影响:系统综述。
Heart Fail Rev. 2024 Jan;29(1):1-11. doi: 10.1007/s10741-023-10336-z. Epub 2023 Aug 9.
10
Dexmedetomidine ameliorates diabetic cardiomyopathy by inhibiting ferroptosis through the Nrf2/GPX4 pathway.右美托咪定通过 Nrf2/GPX4 通路抑制铁死亡改善糖尿病心肌病。
J Cardiothorac Surg. 2023 Jul 10;18(1):223. doi: 10.1186/s13019-023-02300-7.