Ablation of ghrelin receptor reduces adiposity and improves insulin sensitivity during aging by regulating fat metabolism in white and brown adipose tissues

Aging Cell. 2011 Dec;10(6):996-1010. doi: 10.1111/j.1474-9726.2011.00740.x. Epub 2011 Oct 12.

Abstract

Aging is associated with increased adiposity in white adipose tissues and impaired thermogenesis in brown adipose tissues; both contribute to increased incidences of obesity and type 2 diabetes. Ghrelin is the only known circulating orexigenic hormone that promotes adiposity. In this study, we show that ablation of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R) improves insulin sensitivity during aging. Compared to wild-type (WT) mice, old Ghsr(-/-) mice have reduced fat and preserve a healthier lipid profile. Old Ghsr(-/-) mice also exhibit elevated energy expenditure and resting metabolic rate, yet have similar food intake and locomotor activity. While GHS-R expression in white and brown adipose tissues was below the detectable level in the young mice, GHS-R expression was readily detectable in visceral white fat and interscapular brown fat of the old mice. Gene expression profiles reveal that Ghsr ablation reduced glucose/lipid uptake and lipogenesis in white adipose tissues but increased thermogenic capacity in brown adipose tissues. Ghsr ablation prevents age-associated decline in thermogenic gene expression of uncoupling protein 1 (UCP1). Cell culture studies in brown adipocytes further demonstrate that ghrelin suppresses the expression of adipogenic and thermogenic genes, while GHS-R antagonist abolishes ghrelin's effects and increases UCP1 expression. Hence, GHS-R plays an important role in thermogenic impairment during aging. Ghsr ablation improves aging-associated obesity and insulin resistance by reducing adiposity and increasing thermogenesis. Growth hormone secretagogue receptor antagonists may be a new means of combating obesity by shifting the energy balance from obesogenesis to thermogenesis.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, White / metabolism*
  • Adiposity / genetics
  • Aging / genetics*
  • Animals
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / prevention & control
  • Eating / physiology
  • Energy Metabolism / physiology
  • Gene Expression Regulation*
  • Ghrelin / genetics
  • Ghrelin / metabolism
  • Humans
  • Insulin Resistance / genetics
  • Ion Channels / genetics
  • Ion Channels / metabolism
  • Lipid Metabolism / genetics
  • Male
  • Mice
  • Mice, Knockout
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Obesity / complications
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / prevention & control
  • Receptors, Ghrelin / antagonists & inhibitors
  • Receptors, Ghrelin / deficiency*
  • Receptors, Ghrelin / genetics
  • Signal Transduction / genetics*
  • Thermogenesis / physiology
  • Uncoupling Protein 1

Substances

  • Ghrelin
  • Ion Channels
  • Mitochondrial Proteins
  • Receptors, Ghrelin
  • UCP1 protein, human
  • Ucp1 protein, mouse
  • Uncoupling Protein 1