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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.
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页码:588 / 595
页数:8
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