Effect of metformin on insulin-resistant endothelial cell function

被引:13
作者
Chen, Haiyan [1 ]
Li, Jie [1 ]
Yang, Ou [1 ]
Kong, Jian [1 ]
Lin, Guangzhu [2 ]
机构
[1] Jilin Univ, Dept Cardiol, Cadre Ward, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Dept Cardiol, Hosp 1, Changchun 130021, Jilin, Peoples R China
关键词
metformin; insulin resistance; endothelial cells; nitric oxide; endothelial nitric oxide synthase; NITRIC-OXIDE SYNTHASE; CARDIOVASCULAR-DISEASE;
D O I
10.3892/ol.2015.2883
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to investigate the effect of metformin on the function of insulin-resistant (IR) endothelial cells. A model of IR endothelial cells was established by incubating cells with 30 mM glucose, 1 mu M dexamethasone and various concentrations of insulin. The nitric oxide (NO) content of the endothelial cells was determined by measuring the rate of nitroreductase production; the endothelin (ET) concentration was examined by enzyme-linked immunosorbent assay; and the expression levels of endothelial nitric oxide synthase (eNOS) were detected using western blotting. The optimal conditions for inducing insulin resistance in endothelial cells were a combination treatment of 10(-4) mmol/l insulin, 30 mM glucose and 1 mu M dexamethasone for 48 h. Notably, metformin administration significantly increased the NO content and reduced the ET-1 concentration in the IR cells compared with the non-treated control cells (P<0.05); furthermore, metformin significantly increased the intracellular eNOS protein expression in IR endothelial cells compared with the non-treated control cells (P<0.05), with an optimal metformin concentration of 10(-3) mmol/l. Thus, the present study identified that metformin improves the function of IR endothelial cells, possibly through promoting eNOS protein expression and increasing the NO content.
引用
收藏
页码:1149 / 1153
页数:5
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