Honokiol suppresses TNF-α-induced migration and matrix metalloproteinase expression by blocking NF-κB activation via the ERK signaling pathway in rat aortic smooth muscle cells

被引:34
|
作者
Zhu, Xiaoying [1 ,2 ]
Wang, Zhansheng [1 ]
Hu, Cuizhu [1 ]
Li, Zhao [1 ]
Hu, Jian [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Cardiol, Shenyang 110001, Liaoning, Peoples R China
[2] China Med Univ, Affiliated Hosp 1, Gen Hosp, Benxi Iron & Steel Co Ltd,Dept Cardiol, Benxi 117000, Liaoning, Peoples R China
关键词
Honokiol; Vascular smooth muscle cells; Migration; Matrix metalloproteinase-2/9; Nuclear factor-kappa B; ERK; PROTEIN-KINASE; MECHANISMS; ATHEROSCLEROSIS; TRANSCRIPTION; MAGNOLOL; EGR-1; AP-1;
D O I
10.1016/j.acthis.2013.11.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Honokiol, a small-molecule polyphenol derived and isolated from the Chinese medicinal herb Magnolia officinalis, has been shown to possess a wide range of pharmacological activities. In the present study, we aimed to investigate the effects of honokiol on tumor necrosis factor-a (TNF-alpha)-induced migration in rat aortic smooth muscle cells (RASMCs). We found that honokiol inhibited TNF-a-induced RASMC proliferation and migration in a dose-dependent manner. At the molecular level, pretreatment with honokiol blocked TNF-alpha-induced protein expression of matrix metalloproteinase (MMP)-2 and MMP-9, nuclear factor (NF)-kappa B activation, and extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation. Moreover, NF-kappa B inhibitor (BAY 11-7028) and ERK inhibitor (U0126) also mimicked the inhibitory effects of honokiol in TNF-alpha-treated RASMCs. In conclusion, these results indicate that honokiol suppresses TNF-alpha-induced migration and MMP expression by blocking NF-kappa B activation via the ERK signaling pathway in RASMCs. Our findings support honokiol as a promising novel agent for the prevention and treatment of atherosclerosis. (C) 2013 Elsevier GmbH. All rights reserved.
引用
收藏
页码:588 / 595
页数:8
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