The gut microbiota-bile acid axis in cholestatic liver disease.

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2024-07-19 DOI:10.1186/s10020-024-00830-x
Dayan Sun, Chuanping Xie, Yong Zhao, Junmin Liao, Shuangshuang Li, Yanan Zhang, Dingding Wang, Kaiyun Hua, Yichao Gu, Jingbin Du, Guoxian Huang, Jinshi Huang
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Abstract

Cholestatic liver diseases (CLD) are characterized by impaired normal bile flow, culminating in excessive accumulation of toxic bile acids. The majority of patients with CLD ultimately progress to liver cirrhosis and hepatic failure, necessitating liver transplantation due to the lack of effective treatment. Recent investigations have underscored the pivotal role of the gut microbiota-bile acid axis in the progression of hepatic fibrosis via various pathways. The obstruction of bile drainage can induce gut microbiota dysbiosis and disrupt the intestinal mucosal barrier, leading to bacteria translocation. The microbial translocation activates the immune response and promotes liver fibrosis progression. The identification of therapeutic targets for modulating the gut microbiota-bile acid axis represents a promising strategy to ameliorate or perhaps reverse liver fibrosis in CLD. This review focuses on the mechanisms in the gut microbiota-bile acids axis in CLD and highlights potential therapeutic targets, aiming to lay a foundation for innovative treatment approaches.

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胆汁淤积性肝病中的肠道微生物群-胆汁酸轴。
胆汁淤积性肝病(CLD)的特点是正常胆汁流动受阻,最终导致有毒胆汁酸过度积累。由于缺乏有效的治疗方法,大多数胆汁淤积性肝病患者最终会发展为肝硬化和肝功能衰竭,需要进行肝移植。最近的研究强调,肠道微生物群-胆汁酸轴通过各种途径在肝纤维化的进展中起着关键作用。胆汁排泄受阻可诱发肠道微生物群失调,破坏肠道粘膜屏障,导致细菌转运。微生物转运激活免疫反应,促进肝纤维化进展。确定调节肠道微生物群-胆汁酸轴的治疗靶点是改善或逆转慢性肝病患者肝纤维化的有效策略。本综述重点探讨肠道微生物群-胆汁酸轴在慢性肝病中的作用机制,并强调潜在的治疗靶点,旨在为创新治疗方法奠定基础。
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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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