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首页> 外文期刊>Molecular medicine reports >Beneficial effects of Huaiqihuang on hyperglycemia-induced MPC5 podocyte dysfunction through the suppression of mitochondrial dysfunction and endoplasmic reticulum stress
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Beneficial effects of Huaiqihuang on hyperglycemia-induced MPC5 podocyte dysfunction through the suppression of mitochondrial dysfunction and endoplasmic reticulum stress

机译:淮北如何通过抑制线粒体功能障碍和内质网应力,槐奇旺对高血糖诱导的MPC5诱发功能障碍的影响

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摘要

The present study was performed to investigate the effect of Huaiqihuang (HQH) on hyperglycemia (HG)-induced mitochondrial dysfunction and endoplasmic reticulum (ER) stress in MPC5 podocytes. The effects of HQH and HG on cell viability were assessed using an MTT assay. mRNA and protein expression levels were evaluated using reverse transcription-quantitative polymerase chain reaction and western blot analysis, respectively. Cell apoptosis was assessed using terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling, whereas reactive oxygen species production and alterations in mitochondrial membrane potential were assessed using flow cytometry. DNA damage was evaluated using a comet assay. The results demonstrated that treatment of podocytes with HQH markedly suppressed the HG-induced generation of reactive oxygen species. HQH also significantly improved mitochondrial membrane potential in podocytes exposed to HG. When the podocytes were treated with HG, Ca2+ levels were significantly increased, compared with those in the control group, whereas treatment of the podocytes with HQH significantly reversed the HG-induced upregulation of Ca2+ secretion. Treatment of the podocytes with HQH significantly reversed the HG-induced upregulation of glucose-related protein 78 (GRP78) and C/EBP-homologous protein, which were used as indicators of ER stress. Furthermore, GRP78 loss-of-function attenuated HG-induced podocyte dysfunction, including cell apoptosis and DNA damage. In conclusion, beneficial effects of HQH on HG-induced MPC5 podocyte dysfunction were observed, and occurred through the suppression of mitochondrial dysfunction and ER stress.
机译:进行本研究以探讨淮北(HQH)对高血糖(Hg)诱导的线粒体功能障碍和内质网(ER)胁迫在MPC5哆哆ytes中的影响。使用MTT测定评估HQH和Hg对细胞活力的影响。使用逆转录定量聚合酶链反应和Western印迹分析评估mRNA和蛋白表达水平。使用末端脱氧核苷酸转移酶脱氧核酸三磷酸碎片末端标记评估细胞凋亡,而使用流式细胞术评估电力氧态膜电位的反应性氧物种生产和改变。使用彗星测定评估DNA损伤。结果表明,用HQH处理龟粒细胞显着抑制了HG诱导的反应性氧物种产生。 HQH在暴露于HG暴露于Hg的孔细胞中也显着改善了线粒体膜电位。当用Hg处理足细胞时,与对照组中的那些相比,Ca2 +水平显着增加,而HQH的孔径诱导的CA2 +分泌的HG诱导的上调的诱导诱导的Ca2 +分泌的诱导诱导的U2 +分泌的诱导诱导的上调。用HQH的诱导孔诱导的葡萄糖相关蛋白质78(GRP78)和C / EBP-同源蛋白的HG诱导的诱导诱导的诱导的诱导的上调,其用作ER应激的指标。此外,GRP78功能丧失衰减的HG诱导的致孔细胞功能障碍,包括细胞凋亡和DNA损伤。总之,观察到HQH对HG诱导的MPC5致键菌功能障碍的有益效果,并通过抑制线粒体功能障碍和ER应力而发生。

著录项

  • 来源
    《Molecular medicine reports》 |2017年第1期|共7页
  • 作者单位

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

    Zhejiang Univ Sch Med Childrens Hosp Dept Nephrol 57 Zhugan Lane Hangzhou 310003 Zhejiang;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 基础医学;
  • 关键词

    mitochondrial dysfunction; endoplasmic reticulum stress; podocyte; Huaiqihuang;

    机译:线粒体功能障碍;内质网胁迫;podocyte;淮北旺;

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