Greater Effectiveness of ε-Viniferin in Red Wine Than Its Monomer Resveratrol for Inhibiting Vascular Smooth Muscle Cell Proliferation and Migration

被引:55
|
作者
Zghonda, Nahla [1 ]
Yoshida, Shigeki [1 ]
Araki, Masahiro [1 ]
Kusunoki, Miki [1 ]
Mliki, Ahmed [2 ]
Ghorbel, Abdelwahed [2 ]
Miyazaki, Hitoshi [1 ]
机构
[1] Univ Tsukuba, Grad Sch Life & Environm Sci, Ibaraki 3058572, Japan
[2] Ctr Biotechnol, Lab Mol Physiol Grapevine, Tunis, Tunisia
关键词
resveratrol; epsilon-viniferin; vascular smooth muscle cells; nuclear factor-E2-related factor 2; hemeoxygenase-1; LOW-DENSITY-LIPOPROTEIN; TRANS-RESVERATROL; CYCLE PROGRESSION; HEME OXYGENASE-1; POLYPHENOLS; OLIGOSTILBENES; OXIDATION; ANALOGS; RHUBARB; HYPERPLASIA;
D O I
10.1271/bbb.110022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Resveratrol is a strong candidate for explaining an irreversible correlation between red wine consumption and coronary heart disease. The present study examined the effect of epsilon-viniferin, a dehydrodimer of resveratrol, on vascular smooth muscle cells (VSMCs), because epsilon-viniferin functions are poorly understood in spite of its comparable content to resveratrol in red wines and grapes. Both epsilon-viniferin and resveratrol inhibited platelet-derived growth factor-induced cell proliferation, migration, and reactive oxygen species (ROS) production, in addition to inducing nitric oxide generation. epsilon-Viniferin was more effective than resveratrol in these effects, except for inhibiting ROS production. The compounds also increased the expression of the antioxidant enzyme, hemeoxygenase-1, via transcription factor Nrf2. The phosphatidylinositol 3-kinase-Akt pathway was implicated in resveratrol-dependent nuclear Nrf2 accumulation, whereas extracellular signal-regulated kinase and p38 were involved in epsilon-viniferin-induced Nrf2 accumulation. These data suggest that epsilon-viniferin may function more effectively than resveratrol in different mechanisms and cooperatively with resveratrol in preventing atherosclerosis.
引用
收藏
页码:1259 / 1267
页数:9
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