Cross-fostering alleviates depression-like behavior mediated by EAAT2 and SNARE complex in prenatal stress offspring rat

Pharmacol Biochem Behav. 2021 Nov:210:173269. doi: 10.1016/j.pbb.2021.173269. Epub 2021 Sep 4.

Abstract

Previous studies have shown that prenatal stress (PS) can potentially contribute to depression-like behavior in offspring and that this effect may be moderated by cross-fostering. However, the underlying mechanism of this effect remains to be determined. This study aimed to determine the effect of cross-fostering on the expression of EAAT2 and the SNARE complex in the hippocampus and the prefrontal cortex of PS offspring rats and to demonstrate functional effects on depression-like behavior. The impacts of cross-fostering were functionally assessed using the sucrose preference test (SPT), the forced swimming test (FST) and the elevated plus maze (EPM). Quantitative real-time PCR was used to determine changes in the expression of EAAT2 and SNAREs mRNA in the hippocampus and the prefrontal cortex of offspring rats. PS offspring rats showed significantly decreased sucrose preference and prolonged immobility time, while cross-fostering effectively increased sucrose preference and shorten the time of immobility. The expression of EAAT2 mRNA in PS offspring rats was markedly reduced, whilst the core mRNA expression of the SNARE complex increased. Our results provide strong evidence demonstrating that cross-fostering can alleviate depression-like behavior and regulate the abnormal expression levels of EAAT2 mRNA and SNARE complex in the hippocampus and the prefrontal cortex of PS offspring rats. Our findings contribute to further understanding of the pathogenesis of PS-induced depression and may help to inform the future development of novel treatment approaches.

Keywords: Cross-fostering; Depression; EAAT2; Glutamate; Prenatal stress; SNARE.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal
  • Depression / metabolism*
  • Depression / psychology
  • Disease Models, Animal
  • Excitatory Amino Acid Transporter 2 / metabolism*
  • Female
  • Hippocampus / metabolism
  • Prefrontal Cortex
  • Pregnancy
  • Prenatal Exposure Delayed Effects / metabolism*
  • Prenatal Exposure Delayed Effects / psychology
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • SNARE Proteins / metabolism*
  • Stress, Psychological / metabolism*

Substances

  • Excitatory Amino Acid Transporter 2
  • RNA, Messenger
  • SNARE Proteins
  • Slc1a2 protein, rat