Insular cortex mediates approach and avoidance responses to social affective stimuli

Nat Neurosci. 2018 Mar;21(3):404-414. doi: 10.1038/s41593-018-0071-y. Epub 2018 Jan 29.

Abstract

Social animals detect the affective states of conspecifics and utilize this information to orchestrate social interactions. In a social affective preference text in which experimental adult male rats could interact with either naive or stressed conspecifics, the experimental rats either approached or avoided the stressed conspecific, depending upon the age of the conspecific. Specifically, experimental rats approached stressed juveniles but avoided stressed adults. Inhibition of insular cortex, which is implicated in social cognition, and blockade of insular oxytocin receptors disrupted the social affective behaviors. Oxytocin application increased intrinsic excitability and synaptic efficacy in acute insular cortex slices, and insular oxytocin administration recapitulated the behaviors observed toward stressed conspecifics. Network analysis of c-Fos immunoreactivity in 29 regions identified functional connectivity between insular cortex, prefrontal cortex, amygdala and the social decision-making network. These results implicate insular cortex as a key component in the circuit underlying age-dependent social responses to stressed conspecifics.

Publication types

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

MeSH terms

  • Affect / drug effects
  • Affect / physiology*
  • Aging / psychology
  • Animals
  • Avoidance Learning / drug effects
  • Avoidance Learning / physiology*
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / physiology*
  • Exploratory Behavior
  • Female
  • Male
  • Optogenetics
  • Oxytocin / pharmacology
  • Proto-Oncogene Proteins c-fos / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Oxytocin / antagonists & inhibitors
  • Social Environment*
  • Stress, Psychological / psychology
  • Vocalization, Animal

Substances

  • Proto-Oncogene Proteins c-fos
  • Receptors, Oxytocin
  • Oxytocin