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Inhibitory Effect of n ‐Butylidenephthalide on Neointimal Hyperplasia in Balloon Injured Rat Carotid Artery
Author(s) -
Liu WeiShin,
Lin PoCheng,
Chang LiFu,
Harn HorngJyh,
Shiuan David,
Chiou TzyyWen,
Jeng JingRen
Publication year - 2011
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.3377
Subject(s) - neointima , neointimal hyperplasia , medicine , vascular smooth muscle , apoptosis , cell growth , endocrinology , in vivo , biology , restenosis , smooth muscle , stent , biochemistry , microbiology and biotechnology
This investigation was designed to determine the inhibitory effects and mechanisms of n ‐butylidenephthalide (BP) from Angelica sinensis on smooth muscle cell (SMC) proliferation in vitro and in balloon injured rat carotid artery. Treatment of cultured rat aorta SMC‐derived A7r5 cells with 25–100 μg/mL BP significantly inhibited the proliferation and arrested the cell cycle in G 0 /G 1 phase. BP induced the expression and migration of Nur77 from the nucleus to the cytoplasm. Among signal pathways, JNK and p38 MAPK were phosphorylated after BP treatment. In vivo , the neointimal area of common carotid artery 2 weeks after balloon injury reduced significantly in Sprague‐Dawley rats treated with 150–300 mg/kg BP compared with the control. The proliferative activity indicated by immunohistochemical detection of Ki‐67 positive cells in the neointima was significantly decreased in the 60–300 mg/kg BP treatment groups. The apoptotic activity indicated by cleaved caspase‐3 positive cells and Nur77 positive cells in the neointima was significantly increased in rats treated with 60–300 mg/kg BP. This study demonstrated BP inhibited neointimal hyperplasia in balloon injured rat carotid artery due to its dual effects of proliferative inhibition and apoptotic induction on SMCs. Up‐regulation of Nur77 gene may partly explain the antihyperplasia activity of BP on the neointima. Copyright © 2011 John Wiley & Sons, Ltd.