平衡
兴奋剂
肝损伤
巨噬细胞
化学
内科学
药理学
内分泌学
受体
医学
生物化学
体外
作者
Qingmiao Shi,Xue Chen,Yifan Zeng,Qingfei Chu,Shuwen Jiang,Yaqi Zhang,Xin Yuan,Danhua Zhu,Lanjuan Li
标识
DOI:10.1016/j.ijbiomac.2024.138510
摘要
Inflammatory response plays an essential role in the pathogenesis of cholestatic liver injury. PPARα agonists have been shown to regulate bile acid homeostasis and hepatic inflammation. However, the immunoregulatory mechanisms through which PPARα agonists ameliorate cholestatic liver injury remain unclear. In this study, surgical bile duct ligation was performed to establish a mouse model of cholestasis. Our study revealed that PPARα agonist alleviated cholestatic liver injury in mice by suppressing inflammatory response, reducing neutrophil infiltration, and promoting M2-like macrophage polarization. CyTOF analysis showed that PPARα agonist increased the proportion of anti-inflammatory F4/80
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