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A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF-β1/Smad Signaling Pathway

机译:通过TGF-β1/ Smad信号通路,中草草化合物免受大鼠酒精肝纤维化的影响

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摘要

Alcoholic liver fibrosis (ALF) has become a major public health concern owing to its health impacts and the lack of effective treatment strategies for the disease. In this study, we investigated the effect of a compound composed of Chinese herbs Pueraria lobata (Willd.), Salvia miltiorrhiza, Schisandra chinensis, and Silybum marianum on ALF. An ALF model was established. Rats were fed with modified Lieber–Decarli alcohol liquid diet and injected with trace CCl4 at late stage. The rats were then treated with several doses of the compound. Biochemical and fibrosis-relevant parameters were measured from the sera obtained from the rats. Liver tissues were obtained for hematoxylin and eosin and Masson’s trichrome staining. Matrix metalloproteinase-13 and tissue inhibitor of metalloproteinase-1 were determined by immunohistochemistry assays. The mRNA and protein expression levels of transforming growth factor-β1 (TGF-β1), Smad2, Smad3, and Smad7 on the livers were also measured by quantitative polymerase chain reaction and Western blot. Results showed that the compound treatment alleviated pathological lesions in the liver, decreased the serum levels of hyaluronan, laminin, and hydroxyproline, and diminished the expression of hepatic tissue inhibitor of metalloproteinase-1. Compound treatment also increased hepatic matrix metalloproteinase-13 expression and inhibited the TGF-β1/Smad signaling pathway. In conclusion, the compound has a protective effect against ALF in rats, and an underlying mechanism is involved in the TGF-β1/Smad signaling pathway.
机译:由于其健康影响以及缺乏对疾病的有效治疗策略,含酒精肝纤维化(ALF)已成为主要的公共卫生问题。在这项研究中,我们研究了由中草草Pueraria Lobata(Willd。),Salvia Miltiorrhiza,Schisandra Chinensis和Silybum Marianum组成的化合物组成的效果。建立了ALF模型。大鼠用改性的利伯利醇液饮食加入并在晚期注射痕量CCL4。然后用几种剂量的化合物处理大鼠。从大鼠获得的血清测量生化和纤维化相关参数。肝组织是用于苏木精和曙红和Masson的三色染色。通过免疫组织化学测定法测定金属蛋白酶-13和金属蛋白酶-1的组织抑制剂。转化生长因子-β1(TGF-β1),Smad2,Smad3和Smad7的mRNA和蛋白表达水平也通过定量聚合酶链反应和Western印迹测量。结果表明,化合物处理缓解了肝脏中病理病变,降低了透明质酸,层蛋白和羟脯氨酸的血清水平,并降低了金属蛋白酶-1的肝组织抑制剂的表达。复合处理还增加肝基质金属蛋白酶-13表达并抑制TGF-β1/ SMAD信号通路。总之,该化合物对大鼠ALF具有保护作用,并且潜在机制参与了TGF-β1/ SMAD信号通路。

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