Astrocytes control food intake by inhibiting AGRP neuron activity via adenosine A1 receptors

Cell Rep. 2015 May 5;11(5):798-807. doi: 10.1016/j.celrep.2015.04.002. Epub 2015 Apr 23.

Abstract

It is well recognized that feeding behavior in mammals is orchestrated by neurons within the medial basal hypothalamus. However, it remains unclear whether food intake is also under the control of glial cells. Here, we combine chemical genetics, cell-type-specific electrophysiology, pharmacology, and feeding assays to show that stimulation of astrocytes within the medial basal hypothalamus reduces both basal- and ghrelin-evoked food intake. This occurs by a mechanism of adenosine-mediated inactivation of the orexigenic agouti-related peptide (AGRP) neurons in the hypothalamic arcuate nucleus (ARC) via adenosine A1 receptors. Our data suggest that glial cells participate in regulating food intake by modulating extracellular levels of adenosine. These findings reveal the existence of a glial relay circuit that controls feeding behavior, one that might serve as a target for therapeutic intervention in the treatment of appetite disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / metabolism
  • Agouti-Related Protein / metabolism*
  • Animals
  • Arcuate Nucleus of Hypothalamus / metabolism
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Blood-Brain Barrier / metabolism
  • Clozapine / analogs & derivatives
  • Clozapine / pharmacology
  • Eating / drug effects
  • Feeding Behavior / drug effects
  • Ghrelin / pharmacology
  • Leptin / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Neurons / metabolism*
  • Receptor, Adenosine A1 / metabolism*

Substances

  • Agouti-Related Protein
  • Ghrelin
  • Leptin
  • Receptor, Adenosine A1
  • Clozapine
  • Adenosine
  • clozapine N-oxide