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解偶联蛋白2对高糖高脂高尿酸诱导的心肌细胞凋亡的作用及机制

田玥 杨怡 贺磊 侯娟妮 杜劲 陈莎 王挺 裴海峰 杨永健

解放军医学杂志2017,Vol.42Issue(6):520-525,6.
解放军医学杂志2017,Vol.42Issue(6):520-525,6.DOI:10.11855/j.issn.0577-7402.2017.06.08

解偶联蛋白2对高糖高脂高尿酸诱导的心肌细胞凋亡的作用及机制

Effect and mechanism of uncoupling protein 2 on cardiomyocyte apoptosis induced by high glucose, high lipid and high uric acid

田玥 1杨怡 1贺磊 2侯娟妮 2杜劲 2陈莎 2王挺 2裴海峰 2杨永健2

作者信息

  • 1. 646000 四川泸州 西南医科大学临床医学院
  • 2. 610083 成都 成都军区总医院心血管内科
  • 折叠

摘要

Abstract

Objective To investigate the effects of uncoupling protein 2 (UCP2) on the myocardial cells of mice with type 2 diabetes mellitus combined with hyperuricemia (HUA), and clarify the mechanism thereof. Methods The mouse cardiac myocytes (MCM) cultured with 25mmol/L high glucose (HG) medium were divided into two groups: HG plus 300μmol/L sodium palmitate for 18 hours as high glucose and high fat (HG+HF) group, and HG+HF plus 1500μmol/L uric acid (UA) for 18 hours as HG+HF+HUA group. Then the myocardial cells in HG+HF+HUA group, by use or not use UCP2 inhibitor genipin, were further divided into two groups: vehicle group and genipin group. In order to verify the mechanism of UCP2 in myocardial cells injury caused by high glucose, high lipid and high uric acid, the myocardial cells were divided again into genipin group and genipin+N-acetylcysteine (NAC) group. Accordingly, the apoptosis of myocardial cells were measured by flow cytometry at specific time, the mRNA and protein expressions of UCP2 were determined by q-PCR and Western blotting, and the levels of reactive oxygen species (ROS) were detected by DHE staining and ELISA. Results The apoptosis rate of myocardial cells increased obviously, and the expression levels of UCP2 decreased and of ROS elevated significantly in HG+HF+HUA group than in HG+HF group (P<0.05). As the expression levels of UCP2 decreased by genipin intervention, the apoptosis rate of myocardial cells and ROS level in HG+HF+HUA group increased more obviously (P<0.05). In contrast, such an effect was reversed by the application of antioxidants NAC (P<0.05). Conclusion UCP2 can inhibit oxidative stress and alleviate the apoptosis of myocardial cells induced by high glucose, high fat and high uric acid.

关键词

高尿酸血症/糖尿病/解偶联蛋白2/氧化应激/心肌细胞

Key words

hyperuricemia/diabetes mellitus/uncoupling protein 2/oxidative stress/cardiomyocytes

分类

医药卫生

引用本文复制引用

田玥,杨怡,贺磊,侯娟妮,杜劲,陈莎,王挺,裴海峰,杨永健..解偶联蛋白2对高糖高脂高尿酸诱导的心肌细胞凋亡的作用及机制[J].解放军医学杂志,2017,42(6):520-525,6.

基金项目

国家自然科学基金(81500208) (81500208)

四川省科技厅杰出青年基金(2017JQ0012) (2017JQ0012)

四川省科技支持计划项目(2015JY0277) (2015JY0277)

博士后医院管理基金(41732BA)This work was supported by the National Natural Science Foundation of China (81500208), the Science Fund for Distinguished Young Scholars of Sichuan Province (2017JQ0012), the Project of Science and Technology Plan of Sichuan Province (2015JY0277), and the Postdoctoral Startup Funds in Hospital (41732BA) (41732BA)

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