肠道菌群
溃疡性结肠炎
失调
脆弱类杆菌
拟杆菌
岩白菜素
化学
微生物学
代谢组
结肠炎
药理学
生物
生物化学
免疫学
医学
细菌
代谢物
遗传学
抗生素
内科学
有机化学
疾病
作者
Tianqing Huang,Yuxin Chen,Su-Ling Zeng,Yang Lin,Fei Li,Zheng‐Meng Jiang,E‐Hu Liu
标识
DOI:10.1021/acs.jafc.3c09448
摘要
Ulcerative colitis is closely associated with the dysregulation of gut microbiota. There is growing evidence that natural products may improve ulcerative colitis by regulating the gut microbiota. In this research, we demonstrated that bergenin, a naturally occurring isocoumarin, significantly ameliorates colitis symptoms in dextran sulfate sodium (DSS)-induced mice. Transcriptomic analysis and Caco-2 cell assays revealed that bergenin could ameliorate ulcerative colitis by inhibiting TLR4 and regulating NF-κB and mTOR phosphorylation. 16S rRNA sequencing and metabolomics analyses revealed that bergenin could improve gut microbiota dysbiosis by decreasing branched-chain amino acid (BCAA) levels. BCAA intervention mediated the mTOR/p70S6K signaling pathway to exacerbate the symptoms of ulcerative colitis in mice. Notably, bergenin greatly decreased the symbiotic bacteria Bacteroides vulgatus (B. vulgatus), and the gavage of B. vulgatus increased BCAA concentrations and aggravated the symptoms of ulcerative colitis in mice. Our findings suggest that gut microbiota-mediated BCAA metabolism plays a vital role in the protective effect of bergenin on ulcerative colitis, providing novel insights for ulcerative colitis prevention through manipulation of the gut microbiota.
科研通智能强力驱动
Strongly Powered by AbleSci AI