An Inhibitory Effect of Chrysoeriol on Platelet-Derived Growth Factor (PDGF)-Induced Proliferation and PDGF Receptor Signaling in Human Aortic Smooth Muscle Cells

被引:24
|
作者
Cha, Byung-Yoon [1 ]
Shi, Wen Lei [2 ]
Yonezawa, Takayuki [1 ]
Teruya, Toshiaki [1 ]
Nagai, Kazuo [1 ,2 ]
Woo, Je-Tae [1 ,2 ]
机构
[1] Chubu Univ, Res Inst Biol Funct, Aichi 4878501, Japan
[2] Chubu Univ, Dept Biol Chem, Aichi 4878501, Japan
关键词
smooth muscle cell; chrysoeriol; platelet-derived growth factor (PDGF)-induced proliferation; antiproliferative; migration; ASPALATHUS-LINEARIS; NITRIC-OXIDE; MIGRATION; ACTIVATION; EXPRESSION; CHEMOTAXIS; MECHANISMS; CALCIUM; LEAVES; BETA;
D O I
10.1254/jphs.08282FP
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Platelet-derived growth factor (PDGF)-BB is one of the most potent factors in the development and progression of various vascular disorders such as restenosis and atherosclerosis. Chrysoeriol is a flavonoid with antioxidant and anti-inflammatory activities. In this study, we investigated the effect of chrysoeriol on the proliferation of human aortic smooth muscle cells (HASMC). Chrysoeriol significantly inhibited PDGF (20 ng/mL)-induced migration and [H-3]-thymidine incorporation into DNA at concentrations of 5 and 10 mu M Without any cytotoxicity. Chrysoeriol also blocked PDGF-stimulated dissociation of actin filament and inhibited PDGF beta-receptor (R beta) phosphorylation in a concentration-dependent manner. As a result, the down-stream signal transduction pathways of PDGF-R beta including EPK1/2, p38, and Akt phosphorylation, were also inhibited by chrysoeriol in the same pattern. These findings Suggest that in addition to its antioxidant and anti-inflammatory activities, chrysoeriol may be used for the prevention and treatment of vascular diseases and during restenosis after coronary angioplasty.
引用
收藏
页码:105 / 110
页数:6
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