Hypoglycemic effect of resveratrol in type 2 diabetic model db/db mice and its actions in cultured L6 myotubes and RIN-5F pancreatic β-cells

被引:58
|
作者
Minakawa, Miki [1 ]
Kawano, Atutoshi [1 ]
Miura, Yutaka [1 ]
Yagasaki, Kazumi [1 ,2 ]
机构
[1] Tokyo Univ Agr & Technol, Grad Sch Agr, Dept Appl Biol Chem, Fuchu, Tokyo 1838509, Japan
[2] Univ Tokyo, Grad Sch Med, Tokyo 1130033, Japan
基金
日本学术振兴会;
关键词
AMPK signaling; myotube; pancreatic beta-cell; resveratrol; type 2 diabetic db/db mouse; GLYCATION END-PRODUCTS; ACTIVATED PROTEIN-KINASE; ENZYME GENE-EXPRESSION; GLUCOSE-UPTAKE; RED WINE; IN-VIVO; CARDIOVASCULAR EVENTS; SKELETAL-MUSCLE; INVASION; RECEPTOR;
D O I
10.3164/jcbn.10-119
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Resveratrol, a phytoalexin present in the skin of grapes and red wine, has been demonstrated to possess a wide range of health promoting activities including anti-diabetic properties. In the present study, we investigated the effect of resveratrol in both type 2 diabetic mice and cell culture systems. In cultured L6 myotubes, we studied the effect of resveratrol on glucose uptake and translocation of glucose transporter 4 to plasma membrane from the aspects of insulin signaling and AMP-activated protein kinase signaling. In cultured RIN-5F cells, we examined whether resveratrol would protect the pancreas-derived beta-cells from oxidative stress. Resveratrol significantly suppressed the elevation in the fasting blood glucose level and the serum triglyceride and lipid peroxide levels in db/db mice. Resveratrol stimulated glucose uptake and glucose transporter 4 translocation by activating both insulin signaling and AMP-activated protein kinase signaling. Moreover, resveratrol could protect pancreatic beta-cells from advanced glycation end products-induced oxidative stress and apoptosis. From these results, resveratrol is suggested to show anti-diabetic effect by stimulating both insulin-dependent and -independent glucose uptake in muscles and by protecting pancreatic beta-cells from advanced glycation end products-induced oxidative stress and apoptosis.
引用
收藏
页码:237 / 244
页数:8
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