Liver-specific RORα deletion does not affect the metabolic susceptibility to western style diet feeding

Mol Metab. 2019 May:23:82-87. doi: 10.1016/j.molmet.2019.02.010. Epub 2019 Mar 9.

Abstract

Objectives: The nuclear receptor superfamily is a potential target for the development of new treatments for obesity and metabolic diseases. Increasing evidence has pointed towards the retinoic acid-related orphan receptor-alpha (RORα) as an important nuclear receptor involved in several biological processes. RORα full body knockout mice display improved metabolic phenotypes on both chow and high fat (60% fat, 20% carbohydrate) diets, but also have severe behavioral abnormalities. Here we investigated the effect of hepatic RORα by generating mice with liver-specific RORα deletion to elucidate the role of this nuclear receptor on host metabolism.

Methods: 8 week-old mice with liver-specific RORα deletion and littermate controls were fed either chow or western-style diets (40% fat, 40% carbohydrate) for 12 weeks. Metabolic phenotyping was performed at the end of the dietary intervention.

Results: Here, we show that hepatic RORα deletion does not affect the metabolic susceptibility to either chow or western-style diet in terms of glucose metabolism and adiposity.

Conclusions: Our data indicate that liver deletion of RORα does not have a pivotal role in the regulation of hepatic glucose and lipid metabolism on chow or western-style diet.

Keywords: Glucose metabolism; Obesity; RORα; Steatosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, White / metabolism
  • Adiposity / genetics
  • Animals
  • Diet, Vegetarian
  • Diet, Western*
  • Female
  • Gene Knockout Techniques
  • Glucose / metabolism*
  • Hepatocytes / metabolism
  • Insulin Resistance / genetics
  • Lipid Metabolism / genetics*
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nuclear Receptor Subfamily 1, Group F, Member 1 / genetics*
  • Obesity / metabolism

Substances

  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • Rora protein, mouse
  • Glucose