首页> 外文期刊>International journal of molecular medicine >The aqueous extract of Gentianella acuta improves isoproterenol-induced myocardial fibrosis via inhibition of the TGF-beta 1/Smads signaling pathway
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The aqueous extract of Gentianella acuta improves isoproterenol-induced myocardial fibrosis via inhibition of the TGF-beta 1/Smads signaling pathway

机译:GentiaNella Acuta的水质提取物通过抑制TGF-β1/ Smads信号通路而改善异丙酚诱导的心肌纤维化

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摘要

Gentianella acuta (G. acuta) is one of the most commonly used herbs in Chinese Mongolian medicine for the treatment of heart disease. Previously, it was found that G. acuta ameliorated cardiac function and inhibited isoproterenol (ISO)-induced myocardial fibrosis in rats. In this study, the underlying anti-fibrotic mechanism of G. acuta was further elucidated. Histopathological changes in the heart were observed by hematoxylineosin, Masson trichrome and wheat germ agglutinin staining. Relevant molecular events were investigated using immunohistochemistry and western blotting. The results revealed that G. acuta caused improvements in myocardial injury and fibrosis. G. acuta also inhibited collagens I and III and alpha -smooth muscle actin production in heart tissue. G. acuta downregulated the expression of transforming growth factor beta 1 (TGF-beta 1) and notably inhibited the levels of phosphorylation of TGF-beta receptors I and II. Furthermore, G. acuta caused downregulation of the intracellular mothers against decapentaplegic homolog (Smads)2 and 4 expression and inhibited Smads2 and 3 phosphorylation. The results further demonstrated that the mechanism underlying anti-myocardial fibrosis effects of G. acuta was based upon the suppression of the TGF-beta 1/Smads signaling pathway. Therefore, G. acuta may be a potential therapeutic agent for ameliorating myocardial fibrosis.
机译:Gentianella acuta(G.acuta)是中国蒙古医学中最常用的草药之一,用于治疗心脏病。以前,发现G. Acuta改善心脏功能和抑制异丙肾上腺素(ISO) - 诱导大鼠心肌纤维化。在该研究中,进一步阐明了G. Acuta的潜在抗纤维化机制。通过苏木喹蛋白酶,Masson richrome和小麦胚芽凝集素染色观察心脏的组织病理学变化。使用免疫组织化学和蛋白质印迹研究了相关的分子事件。结果表明,G.Acuta导致心肌损伤和纤维化的改善。 G. Acuta还抑制了心脏组织中的胶原蛋白I和III和Alpha-Smooth肌肉肌动蛋白产生。 G. Acuta下调了转化生长因子β1(TGF-β1)的表达,并且特别抑制TGF-β受体I和II的磷酸化水平。此外,G.Acuta引起了对抑制细胞内母亲对抗甲板的母亲(Smads)2和4表达并抑制Smads2和3磷酸化。结果进一步证明了G.Acuta的抗心肌纤维化作用的抗心肌纤维化作用的机制基于TGF-β1/ Smads信号通路的抑制。因此,G.Acuta可以是改善心肌纤维化的潜在治疗剂。

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