Fetal growth restriction mice are more likely to exhibit depression-like behaviors due to stress-induced loss of dopaminergic neurons in the VTA

FASEB J. 2020 Oct;34(10):13257-13271. doi: 10.1096/fj.202000534R. Epub 2020 Aug 29.

Abstract

Fetal growth restriction (FGR) is a severe perinatal complication that can increase risk for mental illness. To investigate the mechanism by which FGR mice develop mental illness in adulthood, we established the FGR mouse model and the FGR mice did not display obvious depression-like behaviors, but after environmental stress exposure, FGR mice were more likely to exhibit depression-like behaviors than control mice. Moreover, FGR mice had significantly fewer dopaminergic neurons in the ventral tegmental area but no difference in serotoninergic neurons in the dorsal raphe. RNA-seq analysis showed that the downregulated genes in the midbrain of FGR mice were associated with many mental diseases and were especially involved in the regulation of NMDA-selective glutamate receptor (NMDAR) activity. Furthermore, the NMDAR antagonist memantine can relieve the stress-induced depression-like behaviors of FGR mice. In summary, our findings provide a theoretical basis for future research and treatment of FGR-related depression.

Keywords: depression; dopaminergic neurons; environmental stress; fetal growth restriction; memantine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Depression / drug therapy
  • Depression / metabolism
  • Depression / pathology*
  • Dopaminergic Neurons / metabolism
  • Dopaminergic Neurons / pathology*
  • Dorsal Raphe Nucleus / metabolism
  • Dorsal Raphe Nucleus / pathology
  • Excitatory Amino Acid Antagonists / therapeutic use
  • Fetal Growth Retardation / metabolism
  • Fetal Growth Retardation / pathology*
  • Male
  • Memantine / therapeutic use
  • Mice
  • Mice, Inbred C57BL
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Receptors, N-Methyl-D-Aspartate / genetics
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Stress, Psychological / metabolism
  • Stress, Psychological / pathology*
  • Ventral Tegmental Area / embryology
  • Ventral Tegmental Area / metabolism*
  • Ventral Tegmental Area / pathology

Substances

  • Excitatory Amino Acid Antagonists
  • Receptors, N-Methyl-D-Aspartate
  • Memantine