Juvenile social defeat stress exposure persistently impairs social behaviors and neurogenesis

Neuropharmacology. 2018 May 1:133:23-37. doi: 10.1016/j.neuropharm.2018.01.016. Epub 2018 Jan 11.

Abstract

Adverse juvenile experiences, including physical abuse, often have negative health consequences later in life. We investigated the influence of social defeat stress exposure as juveniles on neuropsychological behaviors, and the causal role of glucocorticoids in abnormal behaviors and impairment of neurogenesis in mice exposed to the stress. The juvenile (24-day-old) and adult (70-day-old) male C57BL/6J mice were exposed to social defeat stress induced by an aggressive ICR mouse. Social defeat stress exposure as juveniles, even for 1 day, induced persistent social avoidance to the unfamiliar ICR mouse in the social interaction test, but that was not observed in mice exposed to the stress as adults. Social avoidance by the stress exposure as juveniles for 10 consecutive days was observed, when the target mouse was not only unfamiliar ICR but also another C57BL/J mouse, but not an absent or an anesthetized ICR mouse. The stress exposure did not induce anxiety- and depression-like behaviors in spontaneous locomotor activity, elevated plus-maze test, marble-burying test, forced swimming test, or sucrose preference test. Serum corticosterone levels increased immediately after the stress exposure. The hippocampal neurogenesis was suppressed 1 day and 4 weeks after the stress exposure. Administration of mifepristone, a glucocorticoid receptor antagonist, prior to each stress exposure, blocked the persistent social avoidance and suppression of neurogenesis. In conclusion, social avoidance induced by social defeat stress exposure as juveniles are more persistent than that as adults. These social avoidances are associated with suppression of hippocampal neurogenesis via glucocorticoid receptors.

Keywords: Glucocorticoid; Hippocampus; Juvenile; Neurogenesis; Social behaviors; Social defeat stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Analysis of Variance
  • Animals
  • Bromodeoxyuridine / metabolism
  • Disease Models, Animal
  • Exploratory Behavior / drug effects
  • Food Preferences / physiology
  • Hormone Antagonists / pharmacology
  • Interpersonal Relations
  • Ki-67 Antigen / metabolism
  • Locomotion / drug effects
  • Locomotion / physiology
  • Male
  • Maze Learning / drug effects
  • Maze Learning / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Mifepristone / pharmacology
  • Neurogenesis / physiology*
  • Stress, Psychological / pathology*
  • Stress, Psychological / physiopathology*
  • Swimming / psychology

Substances

  • Hormone Antagonists
  • Ki-67 Antigen
  • Mifepristone
  • Bromodeoxyuridine