中国全科医学 ›› 2026, Vol. 29 ›› Issue (32): 4827-4832.DOI: 10.12114/j.issn.1007-9572.2024.0645

• 综述与专论 • 上一篇    

线粒体在脑出血后铁死亡中的调控机制和靶向治疗研究新进展

赵麒羽1,2, 李欣悦1,3, 吴民民1,3, 陈秋欣1,2,*()   

  1. 1.150040 黑龙江省哈尔滨市,黑龙江中医药大学
    2.150040 黑龙江省哈尔滨市,黑龙江中医药大学附属第一医院
    3.150040 黑龙江省哈尔滨市,黑龙江中医药大学附属第二医院
  • 收稿日期:2025-04-10 修回日期:2025-05-30 出版日期:2026-11-15 发布日期:2026-10-10
  • 通讯作者: 陈秋欣

  • 作者贡献:

    赵麒羽负责文章的构思与设计、研究资料的收集与整理、论文撰写;李欣悦、吴民民负责论文修订、文章的质量控制;陈秋欣负责对文章审校、对文章整体负责,监督管理。

  • 基金资助:
    国家自然科学基金青年科学基金项目(82004442); 黑龙江省自然科学基金联合引导项目(LH2022H081)

Regulatory Mechanisms and Targeted Therapeutic Research of Mitochondria in Ferroptosis Following Cerebral Hemorrhage

ZHAO Qiyu1,2, LI Xinyue1,3, WU Minmin1,3, CHEN Qiuxin1,2,*()   

  1. 1. Heilongjiang University of Chinese Medicine, Harbin 150040, China
    2. The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin 150040, China
    3. The Second Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin 150040, China
  • Received:2025-04-10 Revised:2025-05-30 Published:2026-11-15 Online:2026-10-10
  • Contact: CHEN Qiuxin

摘要: 脑出血(ICH)是一种高死亡率和致残率的脑卒中类型,铁死亡在ICH后的继发性损伤中扮演重要角色。线粒体作为细胞代谢和能量产生的中心,在铁死亡中具有重要作用,探索线粒体在铁死亡中的作用对治疗ICH后继发性损伤具有重要意义。本文结合ICH后铁死亡过程,从线粒体活性氧(ROS)和线粒体渗透性转换孔(mPTP)、线粒体三羟酸循环(TCA)、线粒体自噬、线粒体脱氧核糖核酸(mtDNA)、线粒体二氢乳清酸脱氢酶(DHODH)等方面探讨其在铁死亡中的作用,并结合靶向线粒体治疗铁死亡的研究进展,为ICH后继发性损伤的干预提供新思路。

关键词: 脑出血, 线粒体, 铁死亡, 活性氧, 线粒体自噬, 二氢乳清酸脱氢酶

Abstract:

Intracerebral hemorrhage (ICH) is a type of stroke with high mortality and disability rates. Ferroptosis plays a significant role in the secondary injury following ICH. Mitochondria, as the center of cellular metabolism and energy production, has an important role in ferroptosis. Exploring the role of mitochondria in ferroptosis is of great significance for the treatment of secondary injuries after ICH. This article discuss the role of mitochondria in ferroptosis from various aspects, including mitochondrial reactive oxygen species (ROS) and mitochondrial permeability transition pore (mPTP), mitochondrial tricarboxylic acid (TCA) cycle, mitochondrial autophagy, mitochondrial DNA (mtDNA), and mitochondrial dihydroorotate dehydrogenase (DHODH), in the context of ferroptosis following ICH. It also reviews the latest research on targeting mitochondria for the treatment of ferroptosis, providing new insights for the intervention of secondary injuries after ICH.

Key words: Intracerebral hemorrhage, Mitochondria, Ferroptosis, Reactive oxygen species, Mitophagy, Dihydroorotate dehydrogenase

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