A dedicated hypothalamic oxytocin circuit controls aversive social learning

Nature. 2024 Feb;626(7998):347-356. doi: 10.1038/s41586-023-06958-w. Epub 2024 Jan 24.

Abstract

To survive in a complex social group, one needs to know who to approach and, more importantly, who to avoid. In mice, a single defeat causes the losing mouse to stay away from the winner for weeks1. Here through a series of functional manipulation and recording experiments, we identify oxytocin neurons in the retrochiasmatic supraoptic nucleus (SOROXT) and oxytocin-receptor-expressing cells in the anterior subdivision of the ventromedial hypothalamus, ventrolateral part (aVMHvlOXTR) as a key circuit motif for defeat-induced social avoidance. Before defeat, aVMHvlOXTR cells minimally respond to aggressor cues. During defeat, aVMHvlOXTR cells are highly activated and, with the help of an exclusive oxytocin supply from the SOR, potentiate their responses to aggressor cues. After defeat, strong aggressor-induced aVMHvlOXTR cell activation drives the animal to avoid the aggressor and minimizes future defeat. Our study uncovers a neural process that supports rapid social learning caused by defeat and highlights the importance of the brain oxytocin system in social plasticity.

MeSH terms

  • Aggression* / physiology
  • Animals
  • Avoidance Learning* / physiology
  • Cues
  • Fear / physiology
  • Hypothalamus* / cytology
  • Hypothalamus* / metabolism
  • Mice
  • Neural Pathways* / physiology
  • Neuronal Plasticity
  • Neurons* / metabolism
  • Oxytocin* / metabolism
  • Receptors, Oxytocin / metabolism
  • Social Behavior
  • Social Learning* / physiology
  • Supraoptic Nucleus / cytology
  • Supraoptic Nucleus / metabolism
  • Ventromedial Hypothalamic Nucleus / cytology
  • Ventromedial Hypothalamic Nucleus / metabolism

Substances

  • OXTR protein, mouse
  • Oxytocin
  • Receptors, Oxytocin