AMP-kinase regulates food intake by responding to hormonal and nutrient signals in the hypothalamus

Nature. 2004 Apr 1;428(6982):569-74. doi: 10.1038/nature02440.


Obesity is an epidemic in Western society, and causes rapidly accelerating rates of type 2 diabetes and cardiovascular disease. The evolutionarily conserved serine/threonine kinase, AMP-activated protein kinase (AMPK), functions as a 'fuel gauge' to monitor cellular energy status. We investigated the potential role of AMPK in the hypothalamus in the regulation of food intake. Here we report that AMPK activity is inhibited in arcuate and paraventricular hypothalamus (PVH) by the anorexigenic hormone leptin, and in multiple hypothalamic regions by insulin, high glucose and refeeding. A melanocortin receptor agonist, a potent anorexigen, decreases AMPK activity in PVH, whereas agouti-related protein, an orexigen, increases AMPK activity. Melanocortin receptor signalling is required for leptin and refeeding effects on AMPK in PVH. Dominant negative AMPK expression in the hypothalamus is sufficient to reduce food intake and body weight, whereas constitutively active AMPK increases both. Alterations of hypothalamic AMPK activity augment changes in arcuate neuropeptide expression induced by fasting and feeding. Furthermore, inhibition of hypothalamic AMPK is necessary for leptin's effects on food intake and body weight, as constitutively active AMPK blocks these effects. Thus, hypothalamic AMPK plays a critical role in hormonal and nutrient-derived anorexigenic and orexigenic signals and in energy balance.

Publication types

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

MeSH terms

  • Adenylate Kinase / antagonists & inhibitors
  • Adenylate Kinase / chemistry
  • Adenylate Kinase / genetics
  • Adenylate Kinase / metabolism*
  • Animals
  • Body Weight / drug effects
  • Energy Metabolism / drug effects
  • Feeding Behavior / drug effects
  • Feeding Behavior / physiology*
  • Glucose / metabolism
  • Glucose / pharmacology
  • Hormones / metabolism*
  • Hormones / pharmacology
  • Hypothalamus / drug effects
  • Hypothalamus / enzymology*
  • Hypothalamus / physiology*
  • Insulin / metabolism
  • Insulin / pharmacology
  • Leptin / metabolism
  • Leptin / pharmacology
  • Male
  • Mice
  • Models, Biological
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Melanocortin / antagonists & inhibitors
  • Receptors, Melanocortin / metabolism


  • Hormones
  • Insulin
  • Leptin
  • RNA, Messenger
  • Receptors, Melanocortin
  • Adenylate Kinase
  • Glucose