化学
法尼甾体X受体
胆汁淤积
肝损伤
药理学
多药耐药蛋白2
异硫氰酸盐
异硫氰酸荧光素
生物化学
杏仁苷
胆红素
肝保护
酶
内科学
核受体
运输机
谷胱甘肽
ATP结合盒运输机
病理
替代医学
物理
基因
荧光
转录因子
医学
量子力学
作者
Juan Zou,Yuanyuan Li,Jingyi Cai,Xiaotian Peng,Lincong Zhang,Tian Tian,Tianming Wang,Rong Shi,Jiasheng Wu,Yueming Ma
标识
DOI:10.1016/j.jchromb.2022.123570
摘要
Yinchenwuling Fang (YCWLF), a famous traditional Chinese medicine, has been used clinically for cholestatic liver disease treatment. However, quantification analysis for YCWLF components and their pharmacological effects remains largely unknown. Therefore, we aimed to determine the YCWLF components and their activities. Quantification analysis of 12 YCWLF components was performed using a comprehensive ultra-performance liquid chromatography (UPLC) coupled with the triple-quadrupole mass spectrometry method. Then, the anti-cholestasis effect and potential mechanism of YCWLF were performed in a mouse model induced by alpha-naphthyl isothiocyanate (ANIT). YCWLF decreased serum biochemical indicators (ALT, AST, ALP, TBA, TBIL, and DBIL) and ameliorated liver tissue damage in cholestatic mice. Mechanically, YCWLF increased the expression of the farnesoid X receptor (FXR) and its downstream efflux transporters and metabolic enzyme genes, reversed the disordered homeostasis of bile acids, and decreased cholestatic liver injury. Based on the important role of FXR in YCWLF amelioration on cholestasis, a dual-luciferase assay was used to screen the potential agonist of FXR from 12 YCWLF components. Chlorogenic acid, 4-hydroxyacetophenone, scoparone, atractylenolide Ⅰ, atractylenolide Ⅱ, and alisol B 23-acetate exhibited an activity effect of FXR. This study provides novel a therapeutic mechanism and potential active compounds of YCWLF on cholestatic liver injury.
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