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三参通脉合剂通过上调microRNA-146a改善大鼠心肌细胞H9C2的氧化损伤

李然 王振裕 王燕丽 滕菲

四川大学学报(医学版)2024,Vol.55Issue(3):630-634,5.
四川大学学报(医学版)2024,Vol.55Issue(3):630-634,5.DOI:10.12182/20240560601

三参通脉合剂通过上调microRNA-146a改善大鼠心肌细胞H9C2的氧化损伤

Sanshentongmai Mixture Improves Oxidative Damage in Rat Cardiomyocytes H9C2 via Upregulation of microRNA-146a

李然 1王振裕 1王燕丽 1滕菲1

作者信息

  • 1. 首都医科大学附属北京中医医院干部保健科 (北京 100010)
  • 折叠

摘要

Abstract

Objective To investigate the effect of Sanshentongmai(SSTM)mixture on the regulation of oxidative damage to rat cardiomyocytes(H9C2)through microRNA-146a and its mechanism.Methods H9C2 were cultured in vitro,H2O2 was used as an oxidant to create an oxidative damage model in H9C2 cells.SSTM intervention was administered to the H9C2 cells.Then,the changes in H2O2-induced oxidative damage in H9C2 cells and the expression of microRNA-146a were observed to explore the protective effect of SSTM on H9C2 and its mechanism.H9C2 cells cultured in vitro were divided into 3 groups,including a control group,a model group of H2O2-induced oxidative damage(referred to hereafter as the model group),and a group given H2O2 modeling plus SSTM intervention at 500 μg/L for 72 h(referred to hereafter as the treatment group).The cell viability was measured by CCK8 assay.In addition,the levels of N-terminal pro-brain natriuretic peptide(Nt-proBNP),nitric oxide(NO),high-sensitivity C-reactive protein(Hs-CRP),and angiotensin were determined by enzyme-linked immunosorbent assay(ELISA).The expression level of microRNA-146a was determined by real-time PCR(RT-PCR).Result H9C2 cells were pretreated with SSTM at mass concentrations ranging from 200 to 1 500 μg/L.Then,CCK8 assay was performed to measure cell viability and the findings showed that the improvement in cell proliferation reached its peak when the mass concentration of SSTM was 500 μg/L,which was subsequently used as the intervention concentration.ELISA was performed to measure the indicators related to heart failure,including Nt-proBNP,NO,Hs-CRP,and angiotensin Ⅱ.Compared with those of the control group,the expressions of Nt-proBNP and angiotensin Ⅱ in the treatment group were up-regulated(P<0.05),while the expression of NO was down-regulated(P<0.05).There was no significant difference in the expression of Hs-CRP between the treatment group and the control group.These findings indicate that SSTM could effectively ameliorate oxidative damage in H9C2 rat cardiomyocytes.Finally,according to the RT-PCR findings for the expression of microRNA-146a in each group,H2O2 treatment at 15 μmol/L could significantly reduce the expression of microRNA-146a,and the expression of microRNA-146a in the treatment group was nearly doubled compared with that in the model group.There was no significant difference between the treatment group and the control group.Conclusion SSTM can significantly resist the H2O2-induced oxidative damage of H9C2 cells and may play a myocardial protective role by upregulating microRNA-146a.

关键词

大鼠心肌细胞H9C2/三参通脉合剂/氧化损伤/微小RNA-146a

Key words

H9C2 cell line/Sanshentongmai mixture/Oxidative damage/microRNA-146a

引用本文复制引用

李然,王振裕,王燕丽,滕菲..三参通脉合剂通过上调microRNA-146a改善大鼠心肌细胞H9C2的氧化损伤[J].四川大学学报(医学版),2024,55(3):630-634,5.

基金项目

国家自然科学基金(No.8150140342)资助 (No.8150140342)

四川大学学报(医学版)

OA北大核心CSTPCDMEDLINE

1672-173X

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