G蛋白偶联胆汁酸受体
肠道菌群
胆汁酸
新陈代谢
受体
法尼甾体X受体
代谢途径
免疫系统
益生菌
脂质代谢
信号转导
生物
细菌
核受体
生物化学
免疫学
遗传学
基因
转录因子
作者
Min Zhao,Zhao Jiafeng,Huimin Yang,Zirou Ouyang,Chang Lv,Zijun Geng,Jianhong Zhao
标识
DOI:10.1016/j.biopha.2025.118182
摘要
Bile acids are a family of signaling molecules synthesized in the liver and metabolized by gut bacteria. As metabolites of the intestinal microbiota, bile acids bind to various receptors, and affect the metabolism and immune function of the host, including glucose and lipid metabolism, energy homeostasis, and inflammatory response. Conversely, bile acids also shape the composition of the gut microbiota. Given their critical role in physiological regulation, disrupted bile acid signaling is closely linked to metabolic diseases. Consequently, therapeutic strategies targeting bile acids are increasingly being explored. The size, composition, and function of the bile acid pool can be modulated through direct treatments (e.g., bile acid replacement therapy, administration of bile acid receptor agonists/antagonists) or indirect treatments (e.g., gut microbiota modulation, probiotic supplementation), providing new ideas for preventing and treating metabolic diseases.
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