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首页> 外文期刊>Chemico-biological interactions >Resveratrol inhibits high glucose induced collagen upregulation in cardiac fibroblasts through regulating TGF-beta 1-Smad3 signaling pathway
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Resveratrol inhibits high glucose induced collagen upregulation in cardiac fibroblasts through regulating TGF-beta 1-Smad3 signaling pathway

机译:白藜芦醇通过调节TGF-beta 1-Smad3信号通路抑制高糖诱导的心肌成纤维细胞胶原蛋白上调

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Cardiac fibrosis is a common pathological process presented in a variety of diseases, including hypertension and diabetes. Cardiac fibroblasts (CFs) have been identified as the most important participants in the development of cardiac fibrosis. Exposure of cultured CFs to high glucose (HG) or angiotensin II (Ang II) resulted in increased collagen synthesis. Resveratrol (Res) is a natural polyphenol exhibiting anti-fibrosis effects in a number of different organs fibrosis process, whether Res can prevent HG and Ang II induced fibrosis response in CFs remains unclear. The aim of this work was to evaluate the effects of Res in HG and Ang II induced fibrosis response in CFs. We cultured rat CFs in either normal glucose (5.6 mM) or HG (25 mM) media in the presence of Res or not and the changes in collagens synthesis and TGF-beta 1 production were assessed by Real-time PCR, Western blotting, and enzyme linked immunosorbent assay (ELISA). Furthermore, normal and diabetic mice (induced by single dose of streptozotocin (100 mg/kg) via tail vein) receiving Res (10 mg/kg) were used to explore the effects of Res on cardiac fibrosis in vivo. Masson staining and immunohistochemistry were performed to visualize cardiac collagen deposition. Results indicate that CFs exposed to HG condition shows enhanced proliferation rate. Furthermore, in the presence of HG or Ang II, CFs exhibited increased collagens synthesis and TGF-beta 1 production. And these effects were abolished by Res intervention. In vivo results show that diabetic mice exhibit increased collagen deposition in the cardiac compared with the normal mice. And this change was prevented by the treatment of Res. These results suggest that Res possesses a potential antifibrogenic effect in hypertension and diabetes-related cardiac fibrosis. Moreover, the action mechanism is probably associated with its ability to reduce TGF-beta 1 content in CFs. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:心脏纤维化是多种疾病中常见的病理过程,包括高血压和糖尿病。心脏成纤维细胞(CFs)已被确定为心脏纤维化发展中最重要的参与者。培养的CFs暴露于高葡萄糖(HG)或血管紧张素II(Ang II)导致胶原合成增加。白藜芦醇(Res)是一种天然多酚,在许多不同的器官纤维化过程中均表现出抗纤维化作用,目前尚不清楚Res是否可以预防HG和Ang II诱导的CFs纤维化反应。这项工作的目的是评估Res在HG和Ang II诱导的CF中纤维化反应中的作用。我们在存在或不存在Res的情况下,在正常葡萄糖(5.6 mM)或HG(25 mM)培养基中培养大鼠CF,并通过实时PCR,Western印迹和胶原蛋白评估胶原合成和TGF-β1产生的变化。酶联免疫吸附测定(ELISA)。此外,使用接受Res(10 mg / kg)的正常和糖尿病小鼠(通过尾静脉单剂量链脲佐菌素(100 mg / kg)诱导)来研究Res对体内心脏纤维化的影响。进行Masson染色和免疫组化以可视化心脏胶原沉积。结果表明暴露于HG条件的CFs增殖速率增加。此外,在HG或Ang II的存在下,CF表现出增加的胶原蛋白合成和TGF-β1的产生。而且,Res干预消除了这些影响。体内结果显示,与正常小鼠相比,糖尿病小鼠心脏中的胶原蛋白沉积增加。 Res的处理可以防止这种变化。这些结果表明,Res在高血压和糖尿病相关的心脏纤维化中具有潜在的抗纤维化作用。此外,该作用机制可能与其降低CF中TGF-β1含量的能力有关。 (C)2014 Elsevier Ireland Ltd.保留所有权利。

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