Heterozygous Hfe gene deletion leads to impaired glucose homeostasis, but not liver injury in mice fed a high‐calorie diet. Issue 12 (June 2016)

• Record Type: Journal Article
• Authors: Britton, Laurence; Jaskowski, Lesley; Bridle, Kim; Santrampurwala, Nishreen; Reiling, Janske; Musgrave, Nick; Subramaniam, V. Nathan; Crawford, Darrell
• Is Part Of: Physiological reports. Volume 4:Issue 12(2016:Jun.)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2016-06
• Subjects: Diabetes -- iron -- nonalcoholic fatty liver disease -- steatohepatitis; Physiology -- Periodicals; 571
• DOI: 10.14814/phy2.12837
• Languages: English
• ISSNs: 2051-817X

Abstract

Abstract: Heterozygous mutations of the Hfe gene have been proposed as cofactors in the development and progression of nonalcoholic fatty liver disease (NAFLD). Homozygous Hfe deletion previously has been shown to lead to dysregulated hepatic lipid metabolism and accentuated liver injury in a dietary mouse model of NAFLD. We sought to establish whether heterozygous deletion of Hfe is sufficient to promote liver injury when mice are exposed to a high‐calorie diet (HCD). Eight‐week‐old wild‐type and Hfe +/− mice received 8 weeks of a control diet or HCD. Liver histology and pathways of lipid and iron metabolism were analyzed. Liver histology demonstrated that mice fed a HCD had increased NAFLD activity score (NAS), steatosis, and hepatocyte ballooning. However, liver injury was unaffected by Hfe genotype. Hepatic iron concentration (HIC) was increased in Hfe +/− mice of both dietary groups. HCD resulted in a hepcidin‐independent reduction in HIC. Hfe +/− mice demonstrated raised fasting serum glucose concentrations and HOMA‐IR score, despite unaltered serum adiponectin concentrations. Downstream regulators of hepatic de novo lipogenesis (pAKT, SREBP‐1, Fas, Scd1 ) and fatty acid oxidation ( AdipoR2, Pparα, Cpt1 ) were largely unaffected by genotype. In summary, heterozygous Hfe gene deletion is associated with impaired iron and glucose metabolism. However, unlike homozygous Hfe deletion, heterozygous gene deletion did not affect lipid metabolism pathways or liver injury in this model. Abstract : Heterozygous Hfe gene deletion in mice is associated with impaired iron and glucose metabolism. However, unlike homozygous Hfe deletion, heterozygous gene deletion does not affect lipid metabolism pathways or liver injury when mice are exposed to a high‐calorie diet.