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首页> 外文期刊>International journal of molecular medicine >Emodin inhibits tumor necrosis factor-α-induced migration and inflammatory responses in rat aortic smooth muscle cells
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Emodin inhibits tumor necrosis factor-α-induced migration and inflammatory responses in rat aortic smooth muscle cells

机译:大黄素抑制肿瘤坏死因子-α诱导的大鼠主动脉平滑肌细胞迁移和炎症反应

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Emodin, a naturally occurring anthraquinone derivative in oriental herbal medicine, has been shown to exert a variety of pharmacological activities. The goal of this study was to determine the effects of emodin on the modulation of cell proliferation, migration, inflammatory responses, and matrix metalloproteinase (MMP)-2 and MMP-9 expression in tumor necrosis factor (TNF)-α-induced rat aortic smooth muscle cells (RASMCs). Cell proliferation and migration were measured using the MTT assay and the transwell chamber assay, respectively. Quantitative real-time PCR and western blot analysis were used to detect MMP expression. Gel shift was used for analysis of nuclear factor (NF)-κB activation. In addition, the expression of several inflammatory genes was also analyzed. Treatment of RASMCs with emodin significantly and dose-dependently attenuated TNF-α-induced proliferation, migration, mRNA and protein expression of MMP-2 and MMP-9, and NF-κB activation. Furthermore, emodin significantly inhibited TNF-α-evoked inflammatory responses, as demonstrated by the reduction in the expression of inflammatory genes. These results suggest that emodin inhibits TNF-α-induced proliferation, migration, MMP-2 and MMP-9 expression as well as inflammatory responses in cultured RASMCs, supporting the notion that emodin may have potential application in clinical atherosclerosis disease.
机译:大黄素(Emodin)是东方草药中的一种天然存在的蒽醌衍生物,已被证明具有多种药理活性。这项研究的目的是确定大黄素对肿瘤坏死因子(TNF)-α诱导的大鼠主动脉中细胞增殖,迁移,炎症反应以及基质金属蛋白酶(MMP)-2和MMP-9表达的调节作用平滑肌细胞(RASMC)。分别使用MTT测定法和transwell室测定法测量细胞增殖和迁移。实时定量PCR和蛋白质印迹分析用于检测MMP表达。凝胶位移用于分析核因子(NF)-κB活化。此外,还分析了几种炎症基因的表达。用大黄素处理RASMCs显着且剂量依赖性地减弱了TNF-α诱导的MMP-2和MMP-9的增殖,迁移,mRNA和蛋白表达以及NF-κB活化。此外,大黄素可显着抑制TNF-α引起的炎症反应,这可通过降低炎症基因的表达来证明。这些结果表明,大黄素抑制TNF-α诱导的增殖,迁移,MMP-2和MMP-9表达以及培养的RASMC中的炎症反应,从而支持大黄素可能在临床动脉粥样硬化疾病中具有潜在的应用价值。

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