Ablation of ghrelin improves the diabetic but not obese phenotype of ob/ob mice

Cell Metab. 2006 May;3(5):379-86. doi: 10.1016/j.cmet.2006.04.004.

Abstract

Ghrelin and leptin are suggested to regulate energy homeostasis as mutual antagonists on hypothalamic neurons that regulate feeding behavior. We employed reverse genetics to investigate the interplay between ghrelin and leptin. Leptin-deficient mice (ob/ob) are hyperphagic, obese, and hyperglycemic. Unexpectedly, ablation of ghrelin in ob/ob mice fails to rescue the obese hyperphagic phenotype, indicating that the ob/ob phenotype is not a consequence of ghrelin unopposed by leptin. Remarkably, deletion of ghrelin augments insulin secretion in response to glucose challenge and increases peripheral insulin sensitivity; indeed, the hyperglycemia exhibited by ob/ob mice is markedly reduced when ob/ob mice are bred onto the ghrelin(-/-) background. We further demonstrate that ablation of ghrelin reduces expression of Ucp2 mRNA in the pancreas, which contributes toward enhanced glucose-induced insulin secretion. Hence, chronically, ghrelin controls glucose homeostasis by regulating pancreatic Ucp2 expression and insulin sensitivity.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Body Temperature Regulation
  • Body Weight
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / physiopathology
  • Down-Regulation
  • Ghrelin
  • Insulin / blood
  • Ion Channels / genetics
  • Ion Channels / metabolism
  • Leptin / genetics
  • Leptin / metabolism
  • Leptin / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Obese
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Obesity / blood
  • Obesity / metabolism*
  • Obesity / physiopathology
  • Pancreas / metabolism
  • Peptide Hormones / genetics
  • Peptide Hormones / metabolism
  • Peptide Hormones / physiology*
  • Phenotype
  • RNA, Messenger / metabolism
  • Uncoupling Protein 2

Substances

  • Blood Glucose
  • Ghrelin
  • Insulin
  • Ion Channels
  • Leptin
  • Mitochondrial Proteins
  • Peptide Hormones
  • RNA, Messenger
  • Ucp2 protein, mouse
  • Uncoupling Protein 2