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电压依赖性阴离子通道3(VDAC3)在脓毒症心肌损伤动物模型中的变化研究

王佳丽 周慧婷 王娜娜 夏雪霞 曹越 张帆 黄鑫 李娜 黄洁

中国比较医学杂志2025,Vol.35Issue(6):1-11,11.
中国比较医学杂志2025,Vol.35Issue(6):1-11,11.DOI:10.3969/j.issn.1671-7856.2025.06.001

电压依赖性阴离子通道3(VDAC3)在脓毒症心肌损伤动物模型中的变化研究

Changes in voltage-dependent anion channel 3 in an animal model of sepsis-induced myocardial injury

王佳丽 1周慧婷 1王娜娜 1夏雪霞 1曹越 1张帆 1黄鑫 1李娜 1黄洁1

作者信息

  • 1. 苏州大学附属儿童医院,江苏苏州 215003
  • 折叠

摘要

Abstract

Objective To observe changes in voltage-dependent anion channel 3(VDAC3)in a mouse model of sepsis-induced myocardial injury and to explore its potential mechanism.Methods Twenty male C57BL/6J mice were divided randomly into a Sham group and Sepsis group,respectively(n=10 mice per group).Sepsis was induced by the cecal ligation and puncture(CLP).Serum levels of interleukin(IL)-6,tumor necrosis factor(TNF)-α,creatine kinase MB(CK-MB),and cardiac troponin T(cTnT)were detected by enzyme-linked immunosorbent assay.Pathological changes in heart tissue were observed by hematoxylin and eosin staining.Structural and functional changes in the heart were evaluated by echocardiography.Changes in total glutathione,reduced glutathione(GSH),oxidized glutathione,and malondialdehyde(MDA)in heart tissue were detected by spectrophotometry.The morphological structure of mitochondria in mouse cardiomyocytes was observed by transmission electron microscopy.Expression levels of IL-6,IL-1β,VDAC3,glutathione peroxidase 4(GPX4),solute carrier family 7 member 11(SLC7A11),lipocalin-2(LCN2),and prostaglandin-endoperoxide synthase 2(PTGS2)mRNA were detected by real-time quantitative polymerase chain reaction and the localization and expression of VDAC3 and GPX4 proteins in mouse heart tissue were detected by immunofluorescence staining.The correlations between VDAC3 mRNA and GPX4,SLC7A11,PTGS2,LCN2,IL-6,and IL-1β mRNA were analyzed.Expression levels of VDAC3,GPX4,and SLC7A11 proteins were detected by Western blot.Results IL-6,TNF-α,CK-MB,and cTnT levels were significantly higher in the Sepsis group compared with the Sham group(P<0.05).In the Sepsis group,myocardial fibers were torn,the ventricular wall was thickened and edematous,the mitochondrial membrane was ruptured,and mitochondrial cristae were broken or absent.GSH levels were significantly reduced in the Sepsis group(P<0.05)and the lipid peroxide MDA was increased in the Sepsis group(P<0.05)compared with the Sham group.VDAC3,GPX4 and SLC7A11 mRNA and protein levels were all lower in the Sepsis group compared with the Sham group(P<0.05),while expression levels of IL-6,IL-1β,LCN2,and PTGS2 mRNA were increased(P<0.05).VDAC3 mRNA was positively correlated with GPX4 and SLC7A11 mRNA levels,and negatively correlated with LCN2,PTGS2,IL-6,and IL-1β.Conclusions VDAC3 expression decreases in myocardial injury,and it may participate in the occurrence of sepsis-induced myocardial injury by regulating ferroptosis.

关键词

VDAC3/铁死亡/脓毒症/心肌损伤

Key words

VDAC3/ferroptosis/sepsis/myocardial injury

分类

医药卫生

引用本文复制引用

王佳丽,周慧婷,王娜娜,夏雪霞,曹越,张帆,黄鑫,李娜,黄洁..电压依赖性阴离子通道3(VDAC3)在脓毒症心肌损伤动物模型中的变化研究[J].中国比较医学杂志,2025,35(6):1-11,11.

基金项目

国家自然科学基金面上项目(82472207) (82472207)

江苏省科技计划项目(BE2023714) (BE2023714)

姑苏卫生人才项目(GSWS2019015) (GSWS2019015)

苏州市科技发展项目(SKY2023058,SKJY2021108). (SKY2023058,SKJY2021108)

中国比较医学杂志

OA北大核心

1671-7856

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