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首页|期刊导航|中医药导报|黄芩苷通过调控铁死亡减轻H9c2细胞缺氧复氧损伤及其机制研究

黄芩苷通过调控铁死亡减轻H9c2细胞缺氧复氧损伤及其机制研究

李家权 许锦 谭子富 方孝俊

中医药导报2025,Vol.31Issue(2):13-18,6.
中医药导报2025,Vol.31Issue(2):13-18,6.DOI:10.13862/j.cn43-1446/r.2025.02.003

黄芩苷通过调控铁死亡减轻H9c2细胞缺氧复氧损伤及其机制研究

Effect and Mechanism of Baicalin on Hypoxia-Reoxygenation Injury in H9c2 Cells Via Regulating Ferroptosis

李家权 1许锦 2谭子富 1方孝俊1

作者信息

  • 1. 恩施土家族苗族自治州中心医院,湖北 恩施 445000
  • 2. 恩施市中心医院,湖北 恩施 445000
  • 折叠

摘要

Abstract

Objective:To investigate the effect and mechanism of baicalin on hypoxia-reoxygenation injury in H9c2 cells via regulating ferroptosis.Methods:Rat H9c2 cardiomyocytes hypoxia-reoxygenation injury model was constructed with Na2S2O4,followed by baicalin intervention.Cell viability,ROS,mitochondrial membrane potential,and Fe2+levels were measured using assay kits.Western blotting was utilized to evaluate cell PTGS2,NOX2,and GPX4 protein expression levels.Cell Fe2+levels were examined using assay kits after baicalin intervention with PTGS2 agonist BUR1 following Na2S2O4 induction.Results:Baicalin up to 80 μmol/L showed no toxicity to H9c2 cells.Na2S2O4 induced ferroptosis in H9c2 cells,characterized by elevated ROS and Fe2+levels,mitochondrial membrane potential collapse,and significant decrease in GPX4 expression(P<0.05).Baicalin intervention led to decreased ROS and Fe2+levels induced by Na2S2O4,restored mitochondrial membrane potential,markedly increased GPX4 expression(P<0.05),and reversing the process of ferroptosis.After Na2S2O4 induction in H9c2 cells,PTGS2 and NOX4 expression significantly increased(P<0.05),while baicalin markedly reduced the expression of PTGS2 and NOX4 induced by Na2S2O4(P<0.05).Baicalin exhibited good binding activity with PTGS2 and NOX4,with binding energies of-10.65 and-8.82 kcal/mol,respectively.BUR1 could reverse the baicalin-inhibited Fe2+levels.Conclusion:Baicalin demonstrates a clear therapeutic effect on ferroptosis in the hypoxia-reoxygenation injury model established by Na2S2O4-induced H9c2 cells,and its treatment mechanism may be associated with the inhibition of PTGS2 and NOX4 protein expression.

关键词

缺血性心肌病/黄芩苷/铁死亡/大鼠H9c2心肌细胞/Na2S2O4/PTGS2/NOX4

Key words

ischemic cardiomyopathy/baicalin/ferroptosis,rat H9c2 cardiomyocytes/Na2S2O4/PTGS2/NOX4

分类

中医学

引用本文复制引用

李家权,许锦,谭子富,方孝俊..黄芩苷通过调控铁死亡减轻H9c2细胞缺氧复氧损伤及其机制研究[J].中医药导报,2025,31(2):13-18,6.

基金项目

湖北省中医药管理局科研项目(ZY2023F121) (ZY2023F121)

中医药导报

1672-951X

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