• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Deciphering a neuronal circuit that mediates appetite.

Hypothalamic neurons that co-express agouti-related protein (AgRP), neuropeptide Y and γ-aminobutyric acid (GABA) are known to promote feeding and weight gain by integration of various nutritional, hormonal, and neuronal signals. Ablation of these neurons in mice leads to cessation of feeding that is accompanied by activation of Fos in most regions where they project. Previous experiments have indicated that the ensuing starvation is due to aberrant activation of the parabrachial nucleus (PBN) and it could be prevented by facilitating GABA(A) receptor signalling in the PBN within a critical adaptation period. We speculated that loss of GABA signalling from AgRP-expressing neurons (AgRP neurons) within the PBN results in unopposed excitation of the PBN, which in turn inhibits feeding. However, the source of the excitatory inputs to the PBN was unknown. Here we show that glutamatergic neurons in the nucleus tractus solitarius (NTS) and caudal serotonergic neurons control the excitability of PBN neurons and inhibit feeding. Blockade of serotonin (5-HT(3)) receptor signalling in the NTS by either the chronic administration of ondansetron or the genetic inactivation of Tph2 in caudal serotonergic neurons that project to the NTS protects against starvation when AgRP neurons are ablated. Likewise, genetic inactivation of glutamatergic signalling by the NTS onto N-methyl D-aspartate-type glutamate receptors in the PBN prevents starvation. We also show that suppressing glutamatergic output of the PBN reinstates normal appetite after AgRP neuron ablation, whereas it promotes weight gain without AgRP neuron ablation. Thus we identify the PBN as a hub that integrates signals from several brain regions to bidirectionally modulate feeding and body weight.

Pubmed ID: 22419158

Authors

  • Wu Q
  • Clark MS
  • Palmiter RD

Journal

Nature

Publication Data

March 29, 2012

Associated Grants

  • Agency: NIDA NIH HHS, Id: DA024908
  • Agency: NIDA NIH HHS, Id: R01 DA024908
  • Agency: Howard Hughes Medical Institute, Id:
  • Agency: Howard Hughes Medical Institute, Id:

Mesh Terms

  • Agouti-Related Protein
  • Animals
  • Appetite
  • Body Weight
  • Feeding Behavior
  • Female
  • Glutamic Acid
  • Hypothalamus
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons
  • Ondansetron
  • Receptors, GABA-A
  • Receptors, N-Methyl-D-Aspartate
  • Serotonergic Neurons
  • Solitary Nucleus
  • Starvation
  • Weight Gain
  • gamma-Aminobutyric Acid