法尼甾体X受体
栀子花
下调和上调
丁酸
肝损伤
TLR4型
药理学
胆汁酸
丁酸盐
化学
炎症
多药耐药蛋白2
胆汁淤积
内科学
内分泌学
生物化学
核受体
医学
运输机
转录因子
ATP结合盒运输机
替代医学
病理
基因
发酵
作者
Tianming Wang,Tian Tian,Zhenyun Zhu,Su Fang,Lincong Zhang,Xiaotian Peng,Rong Shi,Yuanyuan Li,Jiasheng Wu,Yueming Ma
摘要
positive areas in the liver, and inhibited liver inflammation in cholestatic mice. Butyric acid was the most notable intestinal bacterial metabolite following GPS intervention. NaB activated the transcriptional activity of FXR in vitro, upregulated hepatic FXR and its downstream efflux transporter expression, and ameliorated disordered BA homeostasis in CLI mice. NaB inhibited the toll-like receptor 4/nuclear factor (TLR4/NF-κB) pathway and reduced inflammation and CLI in mice. An FXR antagonist suppressed the effects. In conclusion, GPS increased butyric acid production, which can activate hepatic FXR, reverse BA homeostasis disorder, and inhibit the TLR4/NF-κB inflammatory pathway, exerting protective effects against CLI.
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