Scinovex
article Open AccessTop 1% cited

Conditional Deletion Of Brain-Derived Neurotrophic Factor in the Postnatal Brain Leads to Obesity and Hyperactivity

Molecular Endocrinology · 2001 · Vol. 15(10) · pp. 1748–1757
Maribel RiosGuoping FanCsaba FeketeJoseph F. KellyBrian BatesRalf KuehnRonald M. LechanRudolf Jaenisch

Abstract

Brain-derived neurotrophic factor has been associated previously with the regulation of food intake. To help elucidate the role of this neurotrophin in weight regulation, we have generated conditional mutants in which brain-derived neurotrophic factor has been eliminated from the brain after birth through the use of the cre-loxP recombination system. Brain-derived neurotrophic factor conditional mutants were hyperactive after exposure to stressors and had higher levels of anxiety when evaluated in the light/dark exploration test. They also had mature onset obesity characterized by a dramatic 80-150% increase in body weight, increased linear growth, and elevated serum levels of leptin, insulin, glucose, and cholesterol. In addition, the mutants had an abnormal starvation response and elevated basal levels of POMC, an anorexigenic factor and the precursor for alpha-MSH. Our results demonstrate that brain derived neurotrophic factor has an essential maintenance function in the regulation of anxiety-related behavior and in food intake through central mediators in both the basal and fasted state.

Pancreatic function and diabetesRegulation of Appetite and ObesityNerve injury and regenerationNeurotrophic factorsLeptinBiologyEndocrinologyInternal medicineNeurotrophinBrain-derived neurotrophic factorGlial cell line-derived neurotrophic factorBasal (medicine)Insulin-like growth factor

MeSH terms

AnimalsAnxietyBody WeightBrainFastingFluoxetineHyperglycemiaHyperinsulinismHyperkinesisHypothalamusNeuropeptide YObesityPro-OpiomelanocortinRNA, MessengerSerotonin

Funding

  • National Institutes of Health
  • National Cancer Institute
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.