Bile acid metabolism and signaling, the microbiota, and metabolic disease

胆汁酸 肠道菌群 G蛋白偶联胆汁酸受体 生物 代谢途径 新陈代谢 生物化学 信号转导 法尼甾体X受体 脂质代谢 细胞信号 微生物代谢 受体 CYP8B1 微生物学 细菌 核受体 基因 转录因子 遗传学
作者
Jingwei Cai,Bipin Rimal,Changtao Jiang,John Y.L. Chiang,Andrew D. Patterson
出处
期刊:Pharmacology & Therapeutics [Elsevier BV]
卷期号:237: 108238-108238 被引量:208
标识
DOI:10.1016/j.pharmthera.2022.108238
摘要

The diversity, composition, and function of the bacterial community inhabiting the human gastrointestinal tract contributes to host health through its role in producing energy or signaling molecules that regulate metabolic and immunologic functions. Bile acids are potent metabolic and immune signaling molecules synthesized from cholesterol in the liver and then transported to the intestine where they can undergo metabolism by gut bacteria. The combination of host- and microbiota-derived enzymatic activities contribute to the composition of the bile acid pool and thus there can be great diversity in bile acid composition that depends in part on the differences in the gut bacteria species. Bile acids can profoundly impact host metabolic and immunological functions by activating different bile acid receptors to regulate signaling pathways that control a broad range of complex symbiotic metabolic networks, including glucose, lipid, steroid and xenobiotic metabolism, and modulation of energy homeostasis. Disruption of bile acid signaling due to perturbation of the gut microbiota or dysregulation of the gut microbiota-host interaction is associated with the pathogenesis and progression of metabolic disorders. The metabolic and immunological roles of bile acids in human health have led to novel therapeutic approaches to manipulate the bile acid pool size, composition, and function by targeting one or multiple components of the microbiota-bile acid-bile acid receptor axis.
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