The Novel Chinese Medicine JY5 Formula Alleviates Hepatic Fibrosis by Inhibiting the Notch Signaling Pathway

丹参 羟脯氨酸 体内 药理学 五味子 传统医学 四氯化碳 中医药 肝纤维化 肝星状细胞 肝硬化 医学 四氯化碳 化学 生物化学 生物 病理 内科学 有机化学 生物技术 替代医学
作者
Yadong Fu,Zhun Xiao,Xiaoting Tian,Wei Liu,Xu Zhou,Tao Yang,Yonghong Hu,Xiaoxi Zhou,Jing‐Yuan Fang,Siqi Gao,Dingqi Zhang,Yongping Mu,Hua Zhang,Yiyang Hu,Chenggang Huang,Jiamei Chen,Ping Liu
出处
期刊:Frontiers in Pharmacology [Frontiers Media SA]
卷期号:12: 671152-671152 被引量:26
标识
DOI:10.3389/fphar.2021.671152
摘要

Advanced liver fibrosis can lead to cirrhosis, resulting in an accelerated risk of hepatocellular carcinoma and liver failure. Fuzheng Huayu formula (FZHY) is a traditional Chinese medicine formula treated liver fibrosis in China approved by a Chinese State Food and Drug Administration (NO: Z20050546), composed of Salvia Miltiorrhiza bge., Prunus davidiana (Carr.) Franch., cultured Cordyceps sinensis (BerK.) Sacc. Mycelia, Schisandra chinensis (Turcz.) Baill., Pinus massoniana Lamb., and Gynostemma pentaphyllum (Thunb.) Makino. However, the main active substances and mechanism of FZHY are unclear. The aim of this study is to identify a novel anti-fibrotic compound, which consists of the main active ingredients of FZHY, and investigate its mechanism of pharmacological action. The main active ingredients of FZHY were investigated by quantitative analysis of FZHY extracts and FZHY-treated plasma and liver in rats. The anti-fibrotic composition of the main active ingredients was studied through uniform design in vivo , and its mechanism was evaluated in carbon tetrachloride (CCl 4 )- and bile duct ligation (BDL)-induced liver fibrosis models in rats and mice, and transforming growth factor beta 1-induced LX-2 cell activation model in vitro . A novel Chinese medicine, namely JY5 formula, consisting of salvianolic acid B, schisantherin A, and amygdalin, the main active ingredients of FZHY, significantly alleviated hepatic hydroxyproline content and collagen deposition in CCl 4 -and BDL-induced fibrotic liver in rats and mice. In addition, JY5 inhibited the activation of hepatic stellate cells (HSCs) by inactivating Notch signaling in vitro and in vivo . In this study, we found a novel JY5 formula, which exerted anti-hepatic fibrotic effects by inhibiting the Notch signaling pathway, consequently suppressing HSCs activation. These results provide an adequate scientific basis for clinical research and application of the JY5 formula, which may be a potential novel therapeutic candidate for liver fibrosis.

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