首页|期刊导航|中国现代医学杂志|肠道菌群-胆汁酸-FXR轴在代谢相关脂肪性肝病中的作用机制及治疗干预新进展

肠道菌群-胆汁酸-FXR轴在代谢相关脂肪性肝病中的作用机制及治疗干预新进展OA

Mechanisms and therapeutic advances of the gut microbiota-bile acid-FXR axis in metabolic dysfunction-associated fatty liver disease

中文摘要英文摘要

代谢相关脂肪性肝病(MAFLD)是一种与代谢异常密切相关的慢性肝病,严重威胁肝脏健康与代谢稳态.近年来,肠道菌群-胆汁酸-FXR轴作为肠道菌群、胆汁酸代谢系统与宿主肝肠通路之间的核心调控网络,逐渐成为MAFLD研究的重要方向.肠道菌群通过代谢产物、胆汁酸组成及信号分子调控FXR受体活性,进而影响肝脏脂质合成、炎症反应及纤维化进程,在MAFLD的发生、发展中起关键作用.该文系统综述了肠道菌群-胆汁酸-FXR轴介导肠肝互作的分子机制,探讨了该通路在MAFLD发病中的调控作用及其治疗干预新进展,旨在为MAFLD的精准治疗和微生态干预提供理论依据与研究基础.

Metabolic dysfunction-associated fatty liver disease(MAFLD)is a chronic liver condition closely linked to metabolic disorders and poses a serious threat to hepatic health and systemic metabolic balance.In recent years,the gut microbiota-bile acid-farnesoid X receptor(FXR)axis has emerged as a key regulatory network bridging intestinal microbial communities,bile acid metabolism,and host gut-liver crosstalk,and has become a research hotspot in MAFLD.The gut microbiota regulates FXR activity through microbial metabolites,bile acid composition,and signaling molecules,thereby influencing hepatic lipid synthesis,inflammatory responses,and fibrotic progression,and ultimately playing a critical role in the onset and progression of MAFLD.This review systematically summarizes the molecular mechanisms by which the gut microbiota-bile acid-FXR axis mediates gut-liver interaction,explores its role in the pathogenesis of MAFLD,and highlights recent advances in therapeutic interventions,aiming to provide a theoretical foundation for precision treatment and microbiota-targeted strategies in the management of MAFLD.

潘雁;王红梅;何桥玲

梅州市人民医院,广东梅州 514031梅州市人民医院,广东梅州 514031梅州市人民医院,广东梅州 514031

医药卫生

代谢相关脂肪性肝病肠道菌群胆汁酸FXR轴作用机制干预策略

gut microbiotabile acidsfarnesoid X receptor axismetabolic dysfunction-associated fatty liver diseasemechanismstherapeutic strategies

《中国现代医学杂志》 2026 (12)

51-58,8

广东省自然科学基金(2023A1515011314)

10.3969/j.issn.1005-8982.2026.12.008

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