Resveratrol protects RINm5F pancreatic cells from methylglyoxal-induced apoptosis

被引:14
作者
Cheng, An-Sheng [1 ]
Cheng, Yu-Hsiang [2 ]
Chang, Tsu-Liang [1 ]
机构
[1] Natl Taiwan Univ, Dept Hort & Landscape Architecture, Taipei, Taiwan
[2] Univ Auckland, Dept Sci, Auckland, New Zealand
关键词
Advanced glycation end-products (AGEs); Peroxisome proliferator activated-receptor gamma (PPARgamma); Nuclear factor erythroid 2-related factor 2 (Nrf2); Pancreatic-duodenal homeobox-1 (PDX-1); Insulin; INDUCED INSULIN-RESISTANCE; MEDIATED OXIDATIVE STRESS; GLUCOSE-INDUCED APOPTOSIS; UP-REGULATES NRF2; HIGH-FAT DIET; BETA-CELL; IN-VIVO; ENDOTHELIAL-CELLS; TNF-ALPHA; HYPERGLYCEMIA;
D O I
10.1016/j.jff.2013.07.021
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The effects of resveratrol on the prevention of apoptosis as well as insulin production are unclear. To examine the effects, we treated insulin-secreting beta cells with methylglyoxal (MG), a metabolite known to induce apoptosis and diabetes in the presence or absence of resveratrol. The MG treatment induced the expression of apoptotic signaling molecules and decreased insulin production. Pretreatment with resveratrol resulted in an increase in insulin synthesis via upregulation of peroxisome proliferator-activated receptor gamma (PPARgamma) and pancreatic-duodenal homeobox-1 (PDX-1). Resveratrol also inhibited MG-mediated expression of CCAAT/enhancer-binding protein beta (C/EBPbeta), a negative regulator of insulin production. Moreover, resveratrol strongly activated the expression of nuclear factor erythroid 2-related factor 2 (Nrf2), which resulted in the attenuation of oxidative stress. These results suggest that resveratrol can attenuate MG-induced oxidative stress in pancreatic cells and increase insulin levels. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1774 / 1783
页数:10
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