A two-hit adversity model in developing rats reveals sex-specific impacts on prefrontal cortex structure and behavior

Dev Cogn Neurosci. 2021 Apr:48:100924. doi: 10.1016/j.dcn.2021.100924. Epub 2021 Jan 27.

Abstract

Adversity early in life substantially impacts prefrontal cortex (PFC) development and vulnerability to later-life psychopathology. Importantly, repeated adverse experiences throughout childhood increase the risk for PFC-mediated behavioral deficits more commonly in women. Evidence from animal models points to effects of adversity on later-life neural and behavioral dysfunction; however, few studies have investigated the neurobiological underpinnings of sex-specific, long-term consequences of multiple developmental stressors. We modeled early life adversity in rats via maternal separation (postnatal day (P)2-20) and juvenile social isolation (P21-35). In adulthood, anxiety-like behavior was assessed in the elevated zero maze and the presence and structural integrity of PFC perineuronal nets (PNNs) enwrapping parvalbumin (PV)-expressing interneurons was quantified. PNNs are extracellular matrix structures formed during critical periods in postnatal development that play a key role in the plasticity of PV cells. We observed a female-specific effect of adversity on hyperactivity and risk-assessment behavior. Moreover, females - but not males - exposed to multiple hits of adversity demonstrated a reduction in PFC PV cells in adulthood. We also observed a sex-specific, potentiated reduction in PV + PNN structural integrity. These findings suggest a sex-specific impact of repeated adversity on neurostructural development and implicate PNNs as a contributor to associated behavioral dysfunction.

Keywords: Anxiety; Maternal separation; Parvalbumin; Perineuronal nets; Prefrontal cortex; Sex differences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Female
  • Interneurons / metabolism
  • Male
  • Maternal Deprivation
  • Parvalbumins / metabolism
  • Prefrontal Cortex* / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Parvalbumins