| Literature DB >> 25449276 |
Yan Li1, Xiaoyan Wang5, Zengtao Wei2, Hongju Mao3, Meng Gao1, Yanping Liu1, Yanyan Ma1, Xingli Liu4, Chun Guo1, Lining Zhang1, Xiaoyan Wang5.
Abstract
Intestinal endotoxemia-induced liver injury is a common clinical disease which leads to liver failure and death. Wortmannin, an inhibitor of phosphatidylinositol 3-kinase, could be used for suppressing autophagy in vitro and in vivo. Autophagy is an evolutionarily conserved and lysosome dependent protein degradation pathway, which participates in various physiological and pathological processes. The present study aims to explore the effect of pretreatment with wortmannin on acute liver injury and the autophagy in acute liver injury. We demonstrated that wortmannin could downregulate the expression of phosphorylated extracellular regulated protein kinase and p65, decrease the production and release of hepatic inflammatory cytokines, and then reduce hepatocytes apoptosis and necrosis. More importantly, we found that autophagy was induced to increase in LPS/D-GalN-induced acute liver injury, and pretreatment with wortmannin could effectively inhibit increased autophagy in acute liver injury. In conclusion, these results indicate that wortmannin plays a protective role in LPS/D-GalN induced hepatocytotoxity maybe by inhibiting autophagy and could be acted as a target for the treatment of acute liver injury.Entities:
Keywords: Acute liver injury; Autophagy; Lipopolysaccharide; Wortmannin; d-Galactosamine
Mesh:
Substances:
Year: 2014 PMID: 25449276 DOI: 10.1016/j.bbrc.2014.10.152
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575