Social defeat stress activates medial amygdala cells that express type 2 corticotropin-releasing factor receptor mRNA

Neuroscience. 2009 Aug 4;162(1):5-13. doi: 10.1016/j.neuroscience.2009.03.078. Epub 2009 Apr 7.

Abstract

Defeat is a social stressor involving subordination by a threatening conspecific. Type 2 corticotropin-releasing factor receptors (CRF(2)) are abundant in brain regions implicated in defeat responses and are putative stress-related molecules. The present study sought to determine whether neuroactivation and CRF(2) expression co-occurred at brain region or cellular levels following acute defeat. Male "intruder" Wistar rats were placed into the cage of an aggressive "resident" Long-Evans rat (n=6). Upon defeat, intruders (n=6) were placed in a wire-mesh chamber and were returned to the resident's cage for an additional 75 min. Controls (n=6) were handled and returned to their home cage for the same duration. Coronal brain sections were stained for an immediate early gene product, Fos, as a neuronal activation marker. Combined immunohistochemistry with in situ hybridization was performed on a subset of brain sections from defeated intruders to visualize Fos immunoreactivity and CRF(2) mRNA jointly. Defeated rats had fivefold, sevenfold, and 10-fold more Fos-positive cells than controls in the arcuate, ventromedial nucleus of the hypothalamus, and medial amygdala post-defeat. Significant colocalization of CRF(2) mRNA and Fos-positive cells was observed in the posterior medial amygdala but not in the arcuate nucleus or ventromedial hypothalamus. The results indicate CRF(2) receptor-positive neurons in the posterior medial amygdala are involved in the neural response to social defeat.

Publication types

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

MeSH terms

  • Amygdala / metabolism*
  • Animals
  • Arcuate Nucleus of Hypothalamus / metabolism
  • Dominance-Subordination*
  • Immunohistochemistry
  • In Situ Hybridization
  • Male
  • Neurons / metabolism*
  • Prosencephalon / metabolism
  • Proto-Oncogene Proteins c-fos / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Long-Evans
  • Rats, Wistar
  • Receptors, Corticotropin-Releasing Hormone / metabolism*
  • Stress, Psychological / metabolism*
  • Ventromedial Hypothalamic Nucleus / metabolism

Substances

  • CRF receptor type 2
  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger
  • Receptors, Corticotropin-Releasing Hormone