科研之友
微信
新浪微博
Facebook
分享链接
摘要
Background. To evaluate the AMP-activated protein kinase- (AMPK-) mediated signaling and NF-B-related inflammatory pathways that contribute to cholestatic diseases in the bile duct ligation (BDL) rat model of chronic cholestasis and verify the protective role of 5-Aminoimidazole-4-carboxamide1--D-ribofuranoside (AICAR) against hepatic injury and fibrosis triggered by cholestasis-related inflammation. Methods. Animals were randomly divided into three groups: sham-operated group, BDL group, and BDL AICAR group. Cholestatic liver injury was induced by common BDL. Two weeks later, rats in BDL AICAR group started receiving AICAR treatment. Hepatic pathology was examined by haematoxylin and eosin (H&E) and sirius red staining and hydroxyproline assay was performed in evaluating the severity of hepatic cirrhosis. Real-time PCR and Western blot were performed for RNA gene expression of RNA and protein levels, respectively. Results. The BDL group showed liver injury as evidenced by histological changes and elevation in serum biochemicals, ductular reaction, fibrosis, and inflammation. The mRNA expression of canonical NF-B inflammatory cytokines such as TNF-, IL-1, TGF-, and the protein of noncanonical NF-B, P100, and P52 was upregulated in the livers of BDL rats. The BDL rats with the administration of AICAR could induce AMPK activation inhibiting the noncanonical NF-B pathway to attenuate liver injury and fibrosis in BDL rats. Conclusion. The BDL model of hepatic cholestatic injury resulting in activation of Kupffer cells and recruitment of immune cells might initiate an inflammatory response through activation of the NF-B pathway. The AMPK activator AICAR significantly alleviated BDL-induced inflammation in rats by mainly inhibiting the noncanonical NF-B pathway and thus protecting against hepatic injury and fibrosis triggered by BDL.
- 出版日期2018
- 单位西安交通大学
