某种肠道细菌
法尼甾体X受体
胆酸
胆汁酸
CYP8B1
脂质代谢
化学
G蛋白偶联胆汁酸受体
肠道菌群
胆固醇7α羟化酶
生物化学
生物
核受体
转录因子
基因
作者
Jiaqi Liu,Youhua Liu,Chaoqun Huang,Chuan He,Tongyudan Yang,Ruiti Ren,Zimeng Xin,Xinxia Wang
标识
DOI:10.1002/advs.202412865
摘要
Abstract Global health is increasingly challenged by the growing prevalence of obesity and its associated complications. Quercetin, one of the most important dietary flavonoids, is being explored as an effective therapy for obesity with its mechanism remains understudied. Here in this study, it is demonstrated that quercetin intervention significantly reverses obesity‐related phenotypes through reshaping the overall structure of microbiota, especially boosting colonization of the beneficial gut commensal Akkermansia muciniphila ( A. muciniphila ). Enrichment of A. muciniphila leads to generate more indole‐3‐lactic acid (ILA) to upregulate the expression of 12α‐hydroxylase (CYP8B1) via fat mass and obesity‐associated protein (FTO)/ N 6 ‐methyladenosine (m 6 A)/YTHDF2 manner, thereby facilitating cholesterol converts to cholic acid (CA). CA in turn drastically suppresses lipid accumulation via activating the farnesoid X receptor (FXR) in adipose tissue. This work introduces a novel therapeutic target for addressing obesity and expands upon the current limited understanding of the mediator function of m 6 A modifications in microorganism‐influenced bile acid (BA) metabolism.
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