Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16331
Title: Hepatocyte glutathione peroxidase-1 deficiency improves hepatic glucose metabolism and decreases steatohepatitis in mice
Austin Authors: Merry, Troy L;Tran, Melanie;Dodd, Garron T;Mangiafico, Salvatore P;Wiede, Florian;Kaur, Supreet;McLean, Catriona L;Andrikopoulos, Sofianos;Tiganis, Tony
Affiliation: Metabolic Disease and Obesity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia
Faculty of Medical and Health Sciences, The University of Auckland, Aukland, New Zealand
Department of Medicine, Austin Health, the University of Melbourne, Heidelberg, Victoria, Australia
Department of Anatomical Pathology, Alfred Hospital, Prahran, Victoria, Australia
Issue Date: 15-Sep-2016
metadata.dc.date: 2016-09-15
Publication information: Diabetologia 2016; online first: 15 September
Abstract: AIMS/HYPOTHESIS: In obesity oxidative stress is thought to contribute to the development of insulin resistance, non-alcoholic fatty liver disease and the progression to non-alcoholic steatohepatitis. Our aim was to examine the precise contributions of hepatocyte-derived H2O2 to liver pathophysiology. METHODS: Glutathione peroxidase (GPX) 1 is an antioxidant enzyme that is abundant in the liver and converts H2O2 to water. We generated Gpx1 lox/lox mice to conditionally delete Gpx1 in hepatocytes (Alb-Cre;Gpx1 lox/lox) and characterised mice fed chow, high-fat or choline-deficient amino-acid-defined (CDAA) diets. RESULTS: Chow-fed Alb-Cre;Gpx1 lox/lox mice did not exhibit any alterations in body composition or energy expenditure, but had improved insulin sensitivity and reduced fasting blood glucose. This was accompanied by decreased gluconeogenic and increased glycolytic gene expression as well as increased hepatic glycogen. Hepatic insulin receptor Y1163/Y1163 phosphorylation and Akt Ser-473 phosphorylation were increased in fasted chow-fed Alb-Cre;Gpx1 lox/lox mice, associated with increased H2O2 production and insulin signalling in isolated hepatocytes. The enhanced insulin signalling was accompanied by the increased oxidation of hepatic protein tyrosine phosphatases previously implicated in the attenuation of insulin signalling. High-fat-fed Alb-Cre;Gpx1 lox/lox mice did not exhibit alterations in weight gain or hepatosteatosis, but exhibited decreased hepatic inflammation, decreased gluconeogenic gene expression and increased insulin signalling in the liver. Alb-Cre;Gpx1 lox/lox mice fed a CDAA diet that promotes non-alcoholic steatohepatitis exhibited decreased hepatic lymphocytic infiltrates, inflammation and liver fibrosis. CONCLUSIONS/INTERPRETATION: Increased hepatocyte-derived H2O2 enhances hepatic insulin signalling, improves glucose control and protects mice from the development of non-alcoholic steatohepatitis.
URI: http://ahro.austin.org.au/austinjspui/handle/1/16331
DOI: 10.1007/s00125-016-4084-3
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/27628106
Type: Journal Article
Subjects: Fibrosis
Glutathione peroxidase-1
Hepatocyte
Inflammation
Insulin resistance
Non-alcoholic fatty liver disease
Non-alcoholic steatohepatitis
Protein tyrosine phosphatas
Reactive oxygen species
Type 2 diabetes
Appears in Collections:Journal articles

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