G蛋白偶联胆汁酸受体
胆汁酸
分解代谢
糖异生
内科学
内分泌学
碳水化合物代谢
法尼甾体X受体
新陈代谢
葡萄糖稳态
医学
生物化学
胰岛素
胰岛素抵抗
脂质代谢
化学
核受体
转录因子
基因
作者
José A González-Regueiro,Lidia Moreno-Castañeda,Misael Uribe,Norberto C. Chávez‐Tapia
标识
DOI:10.5604/01.3001.0010.5494
摘要
The gut microbiota has been considered a cornerstone of maintaining the health status of its human host because it not only facilitates harvesting of nutrients and energy from ingested food, but also produces numerous metabolites that can regulate host metabolism. One such class of metabolites, the bile acids, are synthesized from cholesterol in the liver and further metabolized by the gut microbiota into secondary bile acids. These bioconversions modulate the signaling properties of bile acids through the nuclear farnesoid X receptor and the G protein-coupled membrane receptor 5, which regulate diverse metabolic pathways in the host. In addition, bile acids can regulate gut microbial composition both directly and indirectly by activation of innate immune response genes in the small intestine. Therefore, host metabolism can be affected by both microbial modifications of bile acids, which leads to altered signaling via bile acid receptors, and by alterations in the composition of the microbiota. In this review, we mainly describe the interactions between bile acids and intestinal microbiota and their roles in regulating host metabolism, but we also examine the impact of bile acid composition in the gut on the intestinal microbiome and on host physiology.
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