Regulation of social behaviors by p-Stat3 via oxytocin and its receptor in the nucleus accumbens of male Brandt's voles (Lasiopodomys brandtii)

Horm Behav. 2020 Mar:119:104638. doi: 10.1016/j.yhbeh.2019.104638. Epub 2019 Nov 30.

Abstract

Social behavior plays a significant role in the formation of social structure and population regulation in both animals and humans. Oxytocin (OXT) and its receptor (OXTR) are well known for regulating social behaviors, but their upstream regulating factors are rarely investigated. We hypothesized that the phosphorylation of the signal transducer and activator of transcription 3 (p-Stat3) may regulate social and aggressive behaviors via the OXT system in the nucleus accumbens (NAc). To test this hypothesis, OXT, p-Stat3 inhibitor, OXTR antagonist, and OXT plus p-Stat3 inhibitor were infused, respectively, into the NAc in the brain of male Brandt's voles (Lasiopodomys brandtii) - a social rodent species in grassland of Inner Mongolia, China. Our data showed that blockage of p-Stat3-Tyr705 signaling pathway in the NAc not only increased aggressive behavior but also impaired social recognition of male Brandt's voles via its effects on the expression of local OXT and OXTR. These results have illustrated a novel signaling pathway of p-Stat3-Tyr705 in regulating social behaviors via the OXT system.

Keywords: Aggression; Nucleus accumbens; Oxytocin; Signal transducers and activator of transcription 3 (Stat3); Social recognition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggression / drug effects
  • Aggression / physiology
  • Animals
  • Arvicolinae / metabolism
  • Arvicolinae / physiology*
  • Brain / drug effects
  • Brain / metabolism
  • Brain / physiology
  • HeLa Cells
  • Humans
  • Male
  • Nucleus Accumbens / drug effects
  • Nucleus Accumbens / metabolism*
  • Oxytocin / pharmacology
  • Oxytocin / physiology*
  • Phosphorylation / drug effects
  • Protein Kinases / metabolism
  • Pyridines / pharmacology
  • Receptors, Oxytocin / metabolism
  • Receptors, Oxytocin / physiology*
  • Recognition, Psychology / drug effects
  • STAT3 Transcription Factor / metabolism*
  • Social Behavior*
  • Tyrphostins / pharmacology

Substances

  • Pyridines
  • Receptors, Oxytocin
  • STAT3 Transcription Factor
  • Tyrphostins
  • WP1066
  • Oxytocin
  • Protein Kinases