Leptin signaling is required for leucine deprivation-enhanced energy expenditure

J Biol Chem. 2014 Jan 17;289(3):1779-87. doi: 10.1074/jbc.M113.528943. Epub 2013 Dec 3.

Abstract

Leptin signaling in the hypothalamus is crucial in energy homeostasis. We have previously shown that dietary deprivation of the essential amino acid leucine in mice stimulates fat loss by increasing energy expenditure. The involvement of leptin signaling in this regulation, however, has not been reported. Here, we show that leucine deprivation promotes leptin signaling in mice maintained on an otherwise normal diet and restores leptin responses in mice maintained on a high fat diet, a regimen known to induce leptin resistance. In addition, we found that leucine deprivation stimulated energy expenditure, and fat loss was largely blocked in db/db mice homozygous for a mutation in leptin receptor and a knock-in mouse line Y3F with abrogation of leptin receptor Tyr(1138)-mediated signal transducer and activator transcript 3 signaling. Overall, our studies describe a novel link between hypothalamic leptin signaling and stimulation of energy expenditure under leucine deprivation.

Keywords: Energy Metabolism; Fat Loss; Hypothalamus; Leptin; Leucine Deprivation; STAT3; Uncoupling Proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dietary Fats / pharmacology
  • Energy Metabolism*
  • Hypothalamus / metabolism*
  • Leptin / genetics
  • Leptin / metabolism*
  • Leucine / deficiency*
  • Mice
  • Mice, Mutant Strains
  • Mutation
  • Receptors, Leptin / genetics
  • Receptors, Leptin / metabolism
  • Signal Transduction*

Substances

  • Dietary Fats
  • Leptin
  • Receptors, Leptin
  • leptin receptor, mouse
  • Leucine