结肠炎
法尼甾体X受体
化学
炎症性肠病
药理学
信号转导
胆汁酸
微生物群
脱氧胆酸
炎症
受体
代谢途径
发酵
生物化学
G蛋白偶联胆汁酸受体
肠道微生物群
乳酸
细胞信号
医学
不利影响
活性氧
新陈代谢
作者
Teng Wang,Jiantang Wang,Bingxin Huangfu,Xiaoyun He,Kaida Huang
标识
DOI:10.1021/acs.jafc.6c01607
摘要
Inflammatory bowel disease (IBD) is a chronic intestinal disorder that has become a global public health concern. Postbiotics offer advantages in biosafety and reproducibility over probiotics. Here, we demonstrated that live Allobaculum stercoricanis (A. stercoricanis) and its two postbiotic preparations─inactivated bacterial cells (POST) and cell-free fermentation supernatant (CFS)─effectively alleviated dextran sulfate sodium (DSS)-induced colitis in mice. Integrated gut microbiome and serum metabolomics analyses indicated that these interventions may act through modulating bile acid metabolism and Toll-like receptor signaling pathways. Further investigations combining postbiotic metabolomics, network pharmacology, molecular docking, and molecular dynamics simulations identified α-muricholic acid (α-MCA) as a candidate functional metabolite, with the farnesoid X receptor (FXR) as a potential target. We hypothesize that α-MCA may contribute to ameliorating intestinal inflammation through engagement of FXR and suppression of the TLR4/NF-κB signaling pathway. These findings provide new insights into postbiotic-based therapeutic strategies for IBD.
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