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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.
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页码:1259 / 1267
页数:9
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