MC4R deficiency in pigs results in hyperphagia and ultimately hepatic steatosis without high-fat diet

Biochem Biophys Res Commun. 2019 Dec 10;520(3):651-656. doi: 10.1016/j.bbrc.2019.08.016. Epub 2019 Oct 17.

Abstract

Melanocortin 4 receptor (MC4R)-deficient mice had been used for several years to study human nonalcoholic steatohepatitis (NASH). However, although liver pathologic and biochemical indicators have been examined, mice models do not always faithfully display the phenotype of the human disease. In this study, we investigated the MC4R knockout phenotype in miniature pigs. We found that pigs lacking MC4R exhibited hyperorexia, insulin resistance, hyperinsulinemia, disordered lipid metabolism and their livers accumulated significant amounts of fat. We have shown that deletion of MC4R results in hyperphagia and increased body fat, ultimately leading to hepatic steatosis without atherogenic diet.

Keywords: Hepatic steatosis; Hyperorexia; Melanocortin-4 receptor knockout pig.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / pathology
  • Adipose Tissue / pathology
  • Animals
  • Animals, Genetically Modified
  • Cell Enlargement
  • Diet, High-Fat
  • Disease Models, Animal
  • Eating / genetics
  • Eating / physiology
  • Female
  • Gene Knockout Techniques
  • Humans
  • Hyperphagia / etiology*
  • Hyperphagia / genetics
  • Hyperphagia / metabolism
  • Insulin Resistance / genetics
  • Insulin Resistance / physiology
  • Male
  • Mice
  • Non-alcoholic Fatty Liver Disease / etiology*
  • Non-alcoholic Fatty Liver Disease / genetics
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Pregnancy
  • Receptor, Melanocortin, Type 4 / deficiency*
  • Receptor, Melanocortin, Type 4 / genetics
  • Swine
  • Swine, Miniature

Substances

  • Receptor, Melanocortin, Type 4