The First Clinical Medical College, Lanzhou University, Lanzhou, China.
Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
Front Cell Infect Microbiol. 2022 Sep 15;12:945368. doi: 10.3389/fcimb.2022.945368. eCollection 2022.
Liver fibrosis involves the proliferation and deposition of extracellular matrix on liver tissues owing to various etiologies (including viral, alcohol, immune, and metabolic factors), ultimately leading to structural and functional abnormalities in the liver. If not effectively treated, liver fibrosis, a pivotal stage in the path to chronic liver disease, can progress to cirrhosis and eventually liver cancer; unfortunately, no specific clinical treatment for liver fibrosis has been established to date. In liver fibrosis cases, both the gut microbiota and bile acid metabolism are disrupted. As metabolites of the gut microbiota, bile acids have been linked to the progression of liver fibrosis various pathways, thus implying that the gut microbiota-bile acid axis might play a critical role in the progression of liver fibrosis and could be a target for its reversal. Therefore, in this review, we examined the involvement of the gut microbiota-bile acid axis in liver fibrosis progression to the end of discovering new targets for the prevention, diagnosis, and therapy of chronic liver diseases, including liver fibrosis.
肝纤维化是由于各种病因(包括病毒、酒精、免疫和代谢因素)导致肝组织细胞外基质增生和沉积,最终导致肝脏结构和功能异常。如果不能有效治疗,肝纤维化作为慢性肝病发展的关键阶段,可进展为肝硬化,最终发展为肝癌;遗憾的是,迄今为止尚未建立针对肝纤维化的特定临床治疗方法。在肝纤维化病例中,肠道微生物群和胆汁酸代谢均受到破坏。作为肠道微生物群的代谢物,胆汁酸与肝纤维化的进展有关,涉及多种途径,这表明肠道微生物群-胆汁酸轴可能在肝纤维化的进展中发挥关键作用,并且可能成为其逆转的靶点。因此,在本综述中,我们研究了肠道微生物群-胆汁酸轴在肝纤维化进展中的作用,以期为预防、诊断和治疗包括肝纤维化在内的慢性肝病发现新的靶点。