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韩国沿海海星 Asterias amurensis 的乙酸乙酯部分对 MMP-9 活性和表达以及 TNF-α 诱导的人主动脉平滑肌细胞迁移行为具有抑制作用。

Ethylacetate fraction from Korean seaside starfish, Asterias amurensis, has an inhibitory effect on MMP-9 activity and expression and on migration behavior of TNF-α induced human aortic smooth muscle cells.

机构信息

College of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.

出版信息

Toxicol In Vitro. 2011 Jun;25(4):767-73. doi: 10.1016/j.tiv.2011.01.012. Epub 2011 Jan 27.

Abstract

Atherosclerosis is accompanied by the proliferation of human aortic smooth muscle cells (HASMC) and their movement into the intima. Many reports have indicated the involvement of gelatinases (MMP-9 and MMP-2) in this pathogenesis. The ethylacetate fraction from starfish, Asterias amurensis (EFA), harvested from the Korean seaside has an inhibitory effect on MMP-9 and MMP-2 activities, as well as on the expression of MMP-9 in TNF-α induced HASMC in a dose-dependent manner. Also, EFA inhibits the migration of TNF-α induced HASMC in transwells containing gelatin coated plugs. EFA was not cytotoxic to HASMC over the range 0-1mg/ml. By Western-blot analysis, it was revealed that the phosphorylation of extracellular signal regulated kinase (ERK) in TNF-α induced cells was inhibited and nuclear factor kappa B (NF-κB) p65 levels in nuclear extracts were decreased by EFA treatment. In addition, ERK inhibitor (U0126) treated cells exhibited decreased MMP-9 activity in the zymographic assay. From these results, it was found that the gelatinolytic activity was regulated (1) by enzymatic inhibition of both MMP-9 and MMP-2, as well as (2) by the decreased production of MMP-9 via ERK pathways in EFA treated HASMCs. Taken together, it has been shown that EFA has a putative anti-atherosclerotic effect.

摘要

动脉粥样硬化伴随着人类主动脉平滑肌细胞(HASMC)的增殖和它们向内膜迁移。许多报告表明明胶酶(MMP-9 和 MMP-2)参与了这一发病机制。从韩国海边收获的海星(Asterias amurensis)的乙酸乙酯部分(EFA)对 MMP-9 和 MMP-2 的活性以及 TNF-α诱导的 HASMC 中 MMP-9 的表达具有抑制作用,呈剂量依赖性。此外,EFA 抑制 TNF-α诱导的 HASMC 在含有明胶包被塞的 Transwell 中的迁移。EFA 在 0-1mg/ml 范围内对 HASMC 无细胞毒性。通过 Western blot 分析,发现 EFA 处理可抑制 TNF-α诱导细胞中细胞外信号调节激酶(ERK)的磷酸化,并降低核提取物中核因子 kappa B(NF-κB)p65 水平。此外,ERK 抑制剂(U0126)处理的细胞在明胶酶谱分析中 MMP-9 活性降低。从这些结果中可以发现,EFA 通过以下两种方式调节明胶酶活性:(1)酶抑制 MMP-9 和 MMP-2 的活性,以及(2)通过 ERK 途径减少 MMP-9 的产生。综上所述,表明 EFA 具有潜在的抗动脉粥样硬化作用。

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