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丙二醛通过抑制Nrf2/ARE促进肾小球系膜细胞凋亡

赵璐 孙俊波 金小琴

基础医学与临床Issue(1):69-73,5.
基础医学与临床Issue(1):69-73,5.

丙二醛通过抑制Nrf2/ARE促进肾小球系膜细胞凋亡

MDA accelerates the glomerular mesangial cell apoptosis through inhibition of Nrf 2/ARE

赵璐 1孙俊波 1金小琴1

作者信息

  • 1. 河南中医学院第三附属医院内分泌科,河南郑州450008
  • 折叠

摘要

Abstract

Objective To explore the function of MDA on diabetic nephropathy .Methods Glomerular mesangial cells ( GMC) were pretreated with MDA at a final concentrations of 0μmol/L, 1μmol/L, 5μmol/L, 10μmol/L and 50 μmol/L.MTT assay was used to examine the viability of GMC ) .AnnexinV-FITC was used to evaluate effect of MDA on cell apoptosis .RT-PCR and western blot were used to analyze the expression of Nrf 2, HO-1 andγGCL.Results MDA treatment inhibited GMC viability in a dose-dependent manner .MDA at the concentration of more than 5 μmol/L induced mass production of ROS in GMC ( P<0.05 ) .In addition , antioxygen of tBHQ may relieve MDA-induced reduction of cell viability .MDA inhibited the expression of HO-1 , γGCLand Nrf2 ( P <0.05 ) .Conclusions MDA inhibites GMC viability and promotes the cell apoptosis by ROS production through in-hibiting Nrf2/HO-1-γGCL.

关键词

丙二醛/糖尿病肾病/肾小球系膜细胞/活性氧/Nrf2

Key words

malondialdehyde/diabetic nephropathy/glomerular mesangial cell/ROS/Nrf2

分类

医药卫生

引用本文复制引用

赵璐,孙俊波,金小琴..丙二醛通过抑制Nrf2/ARE促进肾小球系膜细胞凋亡[J].基础医学与临床,2015,(1):69-73,5.

基础医学与临床

OACSCDCSTPCD

1001-6325

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