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丹参和黄芪对 TGF-β/Smad/Wnt 通路及大鼠肝纤维化病理过程的影响。

Effects of Salvia miltiorrhiza and Radix astragali on the TGF-β/Smad/Wnt pathway and the pathological process of liver fibrosis in rats.

机构信息

Division of Gastroenterology, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210009, China.

Division of Infectious Diseases, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210009, China.

出版信息

Cell Mol Biol (Noisy-le-grand). 2020 Sep 30;66(6):46-51.

Abstract

Traditional Chinese medicine has made some progress in the study of liver fibrosis, and provides valuable experience for clinical treatment of liver fibrosis. The aim of this study was to investigate the rationality of compatibility use of Salvia miltiorrhiza and Radix astragali on liver fibrosis in rats. For this purpose, the rat model of liver fibrosis was treated with single or different compatibilities of herbals extracts for 4 weeks. Saline and colchicine were set as a negative and positive control, respectively. Liver histopathology, liver function, and expressions of key proteins in the TGF-β/Smad/Wnt pathway were assessed. Results showed that compared with colchicine, herbal extracts showed better ability to reduce deposition of α-SMA and type I collagen, and improve liver function. The effect of R. astragali extracts and 1:1 compound on improving liver fibrosis and liver function was relatively better than other treatment options. The compound groups showed a particularly significant effect on reducing Cyclin D1 expression. It was concluded that the 1:1 compatibility use of S. miltiorrhiza extracts and R. astragali extracts can preferably attenuate liver fibrosis by regulating the expression of TGF-β1 and Cyclin D1.

摘要

传统中药在肝纤维化的研究方面取得了一定进展,为肝纤维化的临床治疗提供了有价值的经验。本研究旨在探讨丹参和黄芪的配伍应用是否合理。为此,采用单一或不同的草药提取物对肝纤维化大鼠进行了 4 周的治疗。生理盐水和秋水仙碱分别作为阴性和阳性对照。评估了肝组织病理学、肝功能以及 TGF-β/Smad/Wnt 通路中关键蛋白的表达。结果表明,与秋水仙碱相比,草药提取物更能减少α-SMA 和 I 型胶原的沉积,改善肝功能。黄芪提取物和 1:1 化合物对改善肝纤维化和肝功能的效果相对优于其他治疗方案。复方组在降低 Cyclin D1 表达方面表现出特别显著的效果。结论:丹参提取物和黄芪提取物 1:1 配伍使用可以通过调节 TGF-β1 和 Cyclin D1 的表达更好地减轻肝纤维化。

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