Ontology highlight
ABSTRACT: Objective
Excess ethanol consumption has serious pathologic consequences. In humans, repeated episodes of binge drinking can lead to liver damage and have adverse effects on other organs such as pancreas and brain. Long term chronic consumption of ethanol can also result in progressive alcoholic liver disease and cirrhosis. Fibroblast growth factor 21 (FGF21) is a metabolic regulator with multiple physiologic functions. FGF21 is a novel biomarker for non-alcoholic fatty liver disease (NAFLD) in humans and limits hepatotoxicity in mice. Therefore, we explored the possibility that FGF21 plays a role in response to ethanol consumption in both humans and mice.Methods
We used a binge drinking paradigm in humans to examine the effect of acute ethanol consumption on circulating FG
SUBMITTER: Desai BN
PROVIDER: S-EPMC5681240 | biostudies-literature | 2017 Nov
REPOSITORIES: biostudies-literature