• 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

糖尿病性心肌病中的铁死亡:从机制到治疗策略。

Ferroptosis in diabetic cardiomyopathy: from its mechanisms to therapeutic strategies.

机构信息

Department of Endocrinology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Department of Pathophysiology, Hebei Medical University, Shijiazhuang, Hebei, China.

出版信息

Front Endocrinol (Lausanne). 2024 Nov 11;15:1421838. doi: 10.3389/fendo.2024.1421838. eCollection 2024.

DOI:10.3389/fendo.2024.1421838
PMID:39588340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11586197/
Abstract

Diabetic cardiomyopathy (DCM) is defined as structural and functional cardiac abnormalities in diabetes, and cardiomyocyte death is the terminal event of DCM. Ferroptosis is iron-dependent oxidative cell death. Evidence has indicated that iron overload and ferroptosis play important roles in the pathogenesis of DCM. Mitochondria, an important organelle in iron homeostasis and ROS production, play a crucial role in cardiomyocyte ferroptosis in diabetes. Studies have shown some anti-diabetic medicines, plant extracts, and ferroptosis inhibitors might improve DCM by alleviating ferroptosis. In this review, we systematically reviewed the evidence of ferroptosis in DCM. Anti-ferroptosis might be a promising therapeutic strategy for the treatment of DCM.

摘要

糖尿病心肌病(DCM)被定义为糖尿病中的结构性和功能性心脏异常,而心肌细胞死亡是 DCM 的终末事件。铁死亡是一种依赖于铁的氧化细胞死亡。有证据表明,铁过载和铁死亡在 DCM 的发病机制中起重要作用。线粒体是铁稳态和 ROS 产生的重要细胞器,在糖尿病中心肌细胞铁死亡中起关键作用。研究表明,一些抗糖尿病药物、植物提取物和铁死亡抑制剂可能通过减轻铁死亡来改善 DCM。在这篇综述中,我们系统地回顾了铁死亡在 DCM 中的证据。抗铁死亡可能是治疗 DCM 的一种很有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53c2/11586197/c8d1bb3d41eb/fendo-15-1421838-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53c2/11586197/c8d1bb3d41eb/fendo-15-1421838-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53c2/11586197/c8d1bb3d41eb/fendo-15-1421838-g001.jpg

相似文献

1
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.
2
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.
3
PACS2/CPT1A/DHODH signaling promotes cardiomyocyte ferroptosis in diabetic cardiomyopathy.PACS2/CPT1A/DHODH信号通路促进糖尿病性心肌病中的心肌细胞铁死亡。
Cardiovasc Diabetol. 2024 Dec 4;23(1):432. doi: 10.1186/s12933-024-02514-6.
4
Ferroptosis: roles and molecular mechanisms in diabetic cardiomyopathy.铁死亡:在糖尿病心肌病中的作用和分子机制。
Front Endocrinol (Lausanne). 2023 Apr 20;14:1140644. doi: 10.3389/fendo.2023.1140644. eCollection 2023.
5
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.
6
Inhibition of CAV1 attenuates diabetic cardiomyopathy through reducing ferroptosis via activating NRF2/GCLC signaling pathway.抑制CAV1通过激活NRF2/GCLC信号通路减少铁死亡,从而减轻糖尿病性心肌病。
Theranostics. 2025 Mar 31;15(11):4989-5006. doi: 10.7150/thno.107367. eCollection 2025.
7
Canagliflozin mitigates ferroptosis and improves myocardial oxidative stress in mice with diabetic cardiomyopathy.卡格列净减轻糖尿病心肌病小鼠的铁死亡并改善心肌氧化应激。
Front Endocrinol (Lausanne). 2022 Oct 14;13:1011669. doi: 10.3389/fendo.2022.1011669. eCollection 2022.
8
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.
9
N6-methyladenosine modification of SPOP relieves ferroptosis and diabetic cardiomyopathy by enhancing ubiquitination of VDAC3.SPOP的N6-甲基腺苷修饰通过增强VDAC3的泛素化来减轻铁死亡和糖尿病性心肌病。
Free Radic Biol Med. 2025 Jan;226:216-229. doi: 10.1016/j.freeradbiomed.2024.11.025. Epub 2024 Nov 15.
10
Ferroptosis: mechanism and role in diabetes-related cardiovascular diseases.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.

引用本文的文献

1
Oxidative stress and ferroptosis in diabetic cardiomyopathy: mechanistic interplay and therapeutic implications.糖尿病性心肌病中的氧化应激与铁死亡:机制相互作用及治疗意义
Apoptosis. 2025 Sep 9. doi: 10.1007/s10495-025-02170-5.
2
Deep phenotyping of a modified diabetic cardiomyopathy mouse model which reflects clinical disease progression.一种反映临床疾病进展的改良糖尿病性心肌病小鼠模型的深度表型分析。
Diabetol Metab Syndr. 2025 Aug 14;17(1):334. doi: 10.1186/s13098-025-01913-3.
3
Antioxidant proteins can be potential targets in ameliorating ferroptosis in diabetic cardiomyopathy: a literature review.

本文引用的文献

1
A Novel Curcumin-Loaded Nanoplatform Alleviates Osteoarthritis by Inhibiting Chondrocyte Ferroptosis.一种新型载姜黄素纳米平台通过抑制软骨细胞铁死亡减轻骨关节炎
Macromol Rapid Commun. 2025 Apr;46(7):e2400495. doi: 10.1002/marc.202400495. Epub 2024 Sep 18.
2
Sulforaphane improves post-resuscitation myocardial dysfunction by inhibiting cardiomyocytes ferroptosis via the Nrf2/IRF1/GPX4 pathway.萝卜硫素通过 Nrf2/IRF1/GPX4 通路抑制心肌细胞铁死亡改善复苏后心肌功能障碍。
Biomed Pharmacother. 2024 Oct;179:117408. doi: 10.1016/j.biopha.2024.117408. Epub 2024 Sep 8.
3
Quercetin Alleviates LPS-Stimulated Myocardial Injury through Regulating ALOX5/PI3K/AKT Pathway in Sepsis.
抗氧化蛋白可能是改善糖尿病性心肌病中铁死亡的潜在靶点:一项文献综述。
Diabetol Metab Syndr. 2025 Jun 7;17(1):199. doi: 10.1186/s13098-025-01773-x.
4
Deciphering Oxidative Stress in Cardiovascular Disease Progression: A Blueprint for Mechanistic Understanding and Therapeutic Innovation.解读心血管疾病进展中的氧化应激:机制理解与治疗创新蓝图
Antioxidants (Basel). 2024 Dec 31;14(1):38. doi: 10.3390/antiox14010038.
槲皮素通过调节脂氧合酶 5/PI3K/AKT 通路缓解脓毒症诱导的心肌损伤。
Cardiovasc Toxicol. 2024 Oct;24(10):1116-1124. doi: 10.1007/s12012-024-09901-1. Epub 2024 Jul 28.
4
Downregulation of the (pro)renin receptor alleviates ferroptosis-associated cardiac pathological changes via the NCOA 4-mediated ferritinophagy pathway in diabetic cardiomyopathy.((前)肾素受体下调通过 NCOA4 介导的铁蛋白自噬途径减轻糖尿病心肌病中铁死亡相关的心脏病理变化。
Int Immunopharmacol. 2024 Sep 10;138:112605. doi: 10.1016/j.intimp.2024.112605. Epub 2024 Jul 3.
5
Histone acetyltransferase Kat2a regulates ferroptosis via enhancing Tfrc and Hmox1 expression in diabetic cardiomyopathy.组蛋白乙酰转移酶 Kat2a 通过增强糖尿病心肌病中的 Tfrc 和 Hmox1 表达来调节铁死亡。
Cell Death Dis. 2024 Jun 10;15(6):406. doi: 10.1038/s41419-024-06771-x.
6
Regulation of cardiac ferroptosis in diabetic human heart failure: uncovering molecular pathways and key targets.糖尿病性人类心力衰竭中心肌铁死亡的调控:揭示分子途径和关键靶点
Cell Death Discov. 2024 Jun 1;10(1):268. doi: 10.1038/s41420-024-02044-w.
7
Berberine ameliorates nonalcoholic fatty liver disease-induced bone loss by inhibiting ferroptosis.小檗碱通过抑制铁死亡改善非酒精性脂肪性肝病引起的骨丢失。
Bone. 2024 Aug;185:117114. doi: 10.1016/j.bone.2024.117114. Epub 2024 May 7.
8
Resveratrol protects cardiomyocytes against ischemia/reperfusion-induced ferroptosis via inhibition of the VDAC1/GPX4 pathway.白藜芦醇通过抑制 VDAC1/GPX4 通路保护心肌细胞免受缺血/再灌注诱导的铁死亡。
Eur J Pharmacol. 2024 May 15;971:176524. doi: 10.1016/j.ejphar.2024.176524. Epub 2024 Mar 30.
9
Inhibition of ferroptosis reverses heart failure with preserved ejection fraction in mice.抑制铁死亡可逆转伴有射血分数保留的心力衰竭的小鼠模型。
J Transl Med. 2024 Feb 24;22(1):199. doi: 10.1186/s12967-023-04734-y.
10
Sulforaphane prevents diabetes-induced hepatic ferroptosis by activating Nrf2 signaling axis.莱菔硫烷通过激活 Nrf2 信号通路预防糖尿病诱导的肝铁死亡。
Biofactors. 2024 Jul-Aug;50(4):810-827. doi: 10.1002/biof.2042. Epub 2024 Feb 1.