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抗氧化剂对葡萄糖诱导的内皮细胞氧化应激和内质网应激的影响。

Effects of antioxidants on glucose-induced oxidative stress and endoplasmic reticulum stress in endothelial cells.

机构信息

Department of Medicine, University of Florida, Jacksonville, United States.

出版信息

Diabetes Res Clin Pract. 2010 Feb;87(2):161-6. doi: 10.1016/j.diabres.2009.10.023. Epub 2009 Nov 24.

DOI:10.1016/j.diabres.2009.10.023
PMID:19939488
Abstract

AIM

Hyperglycemia-induced endothelial cell dysfunction can be the result of increased oxidative stress and concomitant increase in endoplasmic reticulum (ER) stress. To test the extent of coupling between these two stresses, the effect of antioxidant vitamins on glucose-induced oxidative stress and ER stress in endothelial cells were studied.

METHODS

Human umbilical vein endothelial cells (HUVEC) were treated with physiological (5.5mM) or supra-physiological (27.5mM) dextrose concentrations, and ER stress and oxidative stress were measured. Additional experiments were carried out in HUVEC over-expressing exogenous glucose transporter-1 (Glut-1) and treated with 5.5mM dextrose.

RESULTS

Supra-physiological dextrose concentrations increased both ER stress and oxidative stress. However, while oxidative stress could be effectively inhibited with alpha-tocopherol and ascorbic acid, these antioxidants had no effect on ER stress. Increasing intracellular glucose levels by exogenous expression of Glut-1 in endothelial cells also increased oxidative stress and ER stress. Whereas the oxidative stress in these cells was reduced with alpha-tocopherol and ascorbic acid and dimethylsulfoxide, the ER stress could not be ameliorated with alpha-tocopherol and ascorbic acid.

CONCLUSIONS

These results indicate that ER stress can be uncoupled from oxidative stress and antioxidants can ameliorate the latter without altering the ER stress induced by hyperglycemia.

摘要

目的

高血糖诱导的内皮细胞功能障碍可能是氧化应激增加和内质网(ER)应激同时增加的结果。为了测试这两种应激之间的耦合程度,研究了抗氧化维生素对葡萄糖诱导的内皮细胞氧化应激和 ER 应激的影响。

方法

用生理浓度(5.5mM)或超生理浓度(27.5mM)的葡萄糖处理人脐静脉内皮细胞(HUVEC),并测量 ER 应激和氧化应激。在过表达外源性葡萄糖转运蛋白-1(Glut-1)并以 5.5mM 葡萄糖处理的 HUVEC 中进行了额外的实验。

结果

超生理浓度的葡萄糖增加了 ER 应激和氧化应激。然而,尽管α-生育酚和抗坏血酸可以有效抑制氧化应激,但这些抗氧化剂对 ER 应激没有影响。通过在内皮细胞中外源表达 Glut-1 增加细胞内葡萄糖水平也增加了氧化应激和 ER 应激。虽然这些细胞中的氧化应激可以通过α-生育酚、抗坏血酸和二甲基亚砜来减轻,但 ER 应激不能通过α-生育酚和抗坏血酸来改善。

结论

这些结果表明,ER 应激可以与氧化应激解耦,抗氧化剂可以改善后者而不改变高血糖诱导的 ER 应激。

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