Wei Meilin, Tu Wei, Huang Genhua
Department of Endocrinology and Metabolism, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Front Microbiol. 2024 Jun 3;15:1341938. doi: 10.3389/fmicb.2024.1341938. eCollection 2024.
Nonalcoholic fatty liver disease (NAFLD) emerges as the most predominant cause of liver disease, tightly linked to metabolic dysfunction. Bile acids (BAs), initially synthesized from cholesterol in the liver, undergo further metabolism by gut bacteria. Increasingly acknowledged as critical modulators of metabolic processes, BAs have been implicated as important signaling molecules. In this review, we will focus on the mechanism of BAs signaling involved in glucose homeostasis, lipid metabolism, energy expenditure, and immune regulation and summarize their roles in the pathogenesis of NAFLD. Furthermore, gut microbiota dysbiosis plays a key role in the development of NAFLD, and the interactions between BAs and intestinal microbiota is elucidated. In addition, we also discuss potential therapeutic strategies for NAFLD, including drugs targeting BA receptors, modulation of intestinal microbiota, and metabolic surgery.
非酒精性脂肪性肝病(NAFLD)已成为肝病最主要的病因,与代谢功能障碍密切相关。胆汁酸(BAs)最初在肝脏中由胆固醇合成,随后经肠道细菌进一步代谢。BAs日益被认为是代谢过程的关键调节因子,并被视作重要的信号分子。在本综述中,我们将聚焦于BAs信号传导在葡萄糖稳态、脂质代谢、能量消耗及免疫调节中的机制,并总结它们在NAFLD发病机制中的作用。此外,肠道微生物群失调在NAFLD的发展中起关键作用,同时阐明了BAs与肠道微生物群之间的相互作用。另外,我们还讨论了NAFLD的潜在治疗策略,包括靶向BA受体的药物、肠道微生物群的调节以及代谢手术。