Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2

被引:457
作者
Ungvari, Zoltan [1 ]
Bagi, Zsolt [2 ]
Feher, Attila [2 ]
Recchia, Fabio A. [2 ,5 ]
Sonntag, William E.
Pearson, Kevin [3 ,4 ]
de Cabo, Rafael [3 ]
Csiszar, Anna
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Geriatr Med, Reynolds Oklahoma Ctr Aging, Oklahoma City, OK 73104 USA
[2] New York Med Coll, Dept Physiol, Valhalla, NY 10595 USA
[3] NIA, Lab Expt Gerontol, Baltimore, MD 21224 USA
[4] Univ Kentucky, Grad Ctr Nutr Sci, Lexington, KY USA
[5] Scuola St Anna, Sector Med, Pisa, Italy
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2010年 / 299卷 / 01期
基金
美国国家卫生研究院;
关键词
endothelial cell; gracilis; resveratrol; nuclear factor-E-2-related factor-2; NECROSIS-FACTOR-ALPHA; MITOCHONDRIAL SUPEROXIDE-PRODUCTION; VASCULAR OXIDATIVE STRESS; SMALL-MOLECULE ACTIVATORS; SMOOTH-MUSCLE-CELLS; KAPPA-B ACTIVATION; TNF-ALPHA; CORONARY-ARTERIES; NAD(P)H OXIDASE; GENE-EXPRESSION;
D O I
10.1152/ajpheart.00260.2010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ungvari Z, Bagi Z, Feher A, Recchia FA, Sonntag WE, Pearson K, de Cabo R, Csiszar A. Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2. Am J Physiol Heart Circ Physiol 299: H18-H24, 2010. First published April 23, 2010; doi:10.1152/ajpheart.00260.2010.-Epidemiological studies suggest that Mediterranean diets rich in resveratrol are associated with reduced risk of coronary artery disease. Resveratrol was also shown to confer vasoprotection in animal models of type 2 diabetes and aging. However, the mechanisms by which resveratrol exerts its antioxidative vasculoprotective effects are not completely understood. Using a nuclear factor-E-2-related factor-2 (Nrf2)/antioxidant response element-driven luciferase reporter gene assay, we found that in cultured coronary arterial endothelial cells, resveratrol, in a dose-dependent manner, significantly increases transcriptional activity of Nrf2. Accordingly, resveratrol significantly upregulates the expression of the Nrf2 target genes NAD(P)H:quinone oxidoreductase 1, gamma-glutamylcysteine synthetase, and heme oxygenase-1. Resveratrol treatment also significantly attenuated high glucose (30 mM)-induced mitochondrial and cellular oxidative stress (assessed by flow cytometry using MitoSox and dihydroethidine staining). The aforementioned effects of resveratrol were significantly attenuated by the small interfering RNA downregulation of Nrf2 or the overexpression of Kelch-like erythroid cell-derived protein 1, which inactivates Nrf2. To test the effects of resveratrol in vivo, we used mice fed a high-fat diet (HFD), which exhibit increased vascular oxidative stress associated with an impaired endothelial function. In HFD-fed Nrf2(+/+) mice, resveratrol treatment attenuates oxidative stress (assessed by the Amplex red assay), improves acetylcholine-induced vasodilation, and inhibits apoptosis (assessed by measuring caspase-3 activity and DNA fragmentation) in branches of the femoral artery. In contrast, the aforementioned endothelial protective effects of resveratrol were diminished in HFD-fed Nrf2(-/-) mice. Taken together, our results indicate that resveratrol both in vitro and in vivo confers endothelial protective effects which are mediated by the activation of Nrf2.
引用
收藏
页码:H18 / H24
页数:7
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