Plasma levels of inflammatory cytokines and alanine aminotransferase were increased in FGF21 KO mice. FGF21 depletion exacerbated alcohol-induced hepatic steatosis and liver injury, which was associated with increased

activation of genes involved in lipogenesis mediated by SREBP-1c and decreased expression of genes involved in fatty acid p-oxidation mediated by PGC-1α. Hepatic inflammation was higher in alcohol-exposed FGF21 KO mice than controls. Recombinant FGF21 administration reduced alcohol-induced hepatic steatosis and inflammation in WT mice. Conclusion: Alcohol-induced FGF21 expression is a hepatic adaptive response to lipid dysregulation. FGF21 deficiency exacerbates chronic alcohol-induced liver injury in mice via SREBP-1c-mediated regulation in hepatic lipogenesis, PGC-1 α-mediated fatty acid p-oxidation, and TNF-α-mediated inflammation. Developing Selumetinib in vivo strategies targeting FGF21 signaling is KU-57788 solubility dmso a novel treatment approach for alcoholic steatohepatitis. Disclosures: Craig J. McClain – Consulting: Vertex, Gilead, Baxter, Celgene, Nestle, Danisco, Abbott, Genentech; Grant/Research Support: Ocera, Merck, Glaxo SmithKline; Speaking and Teaching: Roche The following people have nothing to disclose: Cuiqing Zhao, Liming Liu, Fengyuan Li, Wenke Feng BACKGROUND:

decreased muscle mass or sarcopenia has been recently recognized as a risk factor for nonalcoholic fatty liver disease (NAFLD) but its mechanisms and consequences has not been tested. AIM: to explore if experimental NAFLD is associated to sarcopenia in mice and assess its association to functional changes and serum insulin growth factor-1 (IGF-1), a liver derived anabolic hormone. METHODS: C57/Bl6 mice were fed with a westernized diet (ALIOS-diet, Am J Physio Gastrointest Liver Physiol 295: G987-G995,

2008.) and fruc tose in drinking water during 16 weeks. Weight gain, viscera fat, serum biochemical parameters, liver histology, hepatic tri glyceride content and morphological and functional evaluation of skeletal muscle Dapagliflozin (gastrocnemius) were carried out. Muscle fiber cross-sectional area (CSA) was determined estimating the minimal Feret’s diameter. In addition, we evaluated myosin protein levels by western blot as marker of muscle atrophy. Muscle strength was estimated by electro stimulation. IGF-1 serum levels were measured using a commercially available ELISA. RESULTS: The ALIOS diet induced significant weigh gain and NAFLD with a significant increase in hepatic triglycer ide content (23,97±7.9 mg/g liver vs. 2,47±1,5 mg/g liver in chow-fed mice, p<0.05), hepatic steatosis and inflammation as well as increased visceral fat (size of epydidimal pad: 0,76 g±0.33 vs. 0.33±0.07 g in chow-fed mice).