Zhou YueHua, Zhou YunZhong, Li YiFei, Sun Wei, Wang ZhaoLong, Chen Long, He Ye, Niu XiaoLong, Chen Jialiang, Yao Guangtao
Shanghai Innovation Center of TCM Health Service, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Institute of Pharmaceutical Preparation Research, Jinghua Pharmaceutical Group Co., Ltd., Jiangsu, China.
Front Pharmacol. 2022 Aug 19;13:959074. doi: 10.3389/fphar.2022.959074. eCollection 2022.
Multiple types of liver diseases, particularly cholestatic liver diseases (CSLDs) and biliary diseases, can disturb bile acid (BA) secretion; however, BA accumulation is currently seen as an important incentive of various types of liver diseases' progression. Da-Chai-Hu decoction (DCHD) has long been used for treating cholestatic liver diseases; however, the exact mechanisms remain unclear. Currently, our study indicates that the liver damage and cholestasis status of the α-naphthylisothiocyanate (ANIT)-induced intrahepatic cholestasis and bile duct ligation (BDL)-induced extrahepatic cholestasis, following DCHD treatment, were improved; the changes of BA metabolism post-DCHD treatment were investigated by targeted metabolomics profiling by UPLC-MS/MS. DCHD treatment severely downregulated serum biochemical levels and relieved inflammation and the corresponding pathological changes including necrosis, inflammatory infiltration, ductular proliferation, and periductal fibrosis in liver tissue. The experimental results suggested that DCHD treatment altered the size, composition, and distribution of the BAs pool, led the BAs pool of the serum and liver to sharply shrink, especially TCA and TMCA, and enhanced BA secretion into the gallbladder and the excretion of BAs by the urinary and fecal pathway; the levels of BAs synthesized by the alternative pathway were increased in the liver, and the conjugation of BAs and the pathway of BA synthesis were actually affected. In conclusion, DCHD ameliorated ANIT- and BDL-induced cholestatic liver injury by reversing the disorder of BAs profile.
多种类型的肝脏疾病,尤其是胆汁淤积性肝病(CSLDs)和胆道疾病,会干扰胆汁酸(BA)的分泌;然而,目前BA的积累被视为各类肝脏疾病进展的重要诱因。大柴胡汤(DCHD)长期以来一直用于治疗胆汁淤积性肝病;然而,确切机制仍不清楚。目前,我们的研究表明,在DCHD治疗后,α-萘异硫氰酸酯(ANIT)诱导的肝内胆汁淤积和胆管结扎(BDL)诱导的肝外胆汁淤积的肝损伤和胆汁淤积状态得到改善;通过超高效液相色谱-串联质谱(UPLC-MS/MS)靶向代谢组学分析研究了DCHD治疗后BA代谢的变化。DCHD治疗显著下调了血清生化水平,减轻了炎症以及肝脏组织中的相应病理变化,包括坏死、炎症浸润、小胆管增生和胆管周围纤维化。实验结果表明,DCHD治疗改变了BA池的大小、组成和分布,导致血清和肝脏中的BA池急剧缩小,尤其是三羟胆酸(TCA)和鹅脱氧胆酸(TMCA),并增强了BA向胆囊的分泌以及通过尿液和粪便途径的排泄;肝脏中通过替代途径合成的BA水平增加,BA的结合以及BA合成途径实际上受到了影响。总之,DCHD通过逆转BA谱的紊乱改善了ANIT和BDL诱导的胆汁淤积性肝损伤。