Female early adult depression results in detrimental impacts on the behavioral performance and brain development in offspring

CNS Neurosci Ther. 2012 Jun;18(6):461-70. doi: 10.1111/j.1755-5949.2012.00324.x.

Abstract

Aims: The present study was to understand whether early adult depressive females implicated their offspring.

Methods: Seven-week-old female mice were subject to chronic mild stress (CMS) to establish the animal model of depression. The behavioral performance of their offspring were tested via neonatal reflexes tests, hole-board test, and morris water maze test in different ages. Astrocyte number, hippocampal volume, and neurogenesis were analyzed via immunohistochemical blotting. Glucocorticoid receptor (GR) expression and serum cortisol levels were measured by western blotting and ELISA.

Results: Female depressive mice had normal fertility, but their offspring had lowered neonatal survival rate and body weight from neonatal period to early adulthood. The offspring of female depressive mice exhibited the impairments of neonatal reflex attainment and memory, but had higher emotionality as adults. Furthermore, the astrocyte number, hippocampal volume, and neurogenesis were reduced in the offspring. However, the expressions of GR were increased in the hippocampus of offspring.

Conclusion: This study reveals that female early adult depressive mice have normal reproductive ability, but make long-term detrimental impacts on the behavioral performance and brain development of their offspring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Astrocytes / pathology
  • Behavior, Animal / physiology*
  • Body Weight
  • Brain / growth & development*
  • Brain / pathology*
  • Bromodeoxyuridine / metabolism
  • Cell Proliferation
  • Corticosterone / blood
  • Depression / blood
  • Depression / pathology*
  • Depression / physiopathology*
  • Disease Models, Animal
  • Female
  • Food Preferences
  • Freezing Reaction, Cataleptic / physiology
  • Gene Expression Regulation, Developmental / physiology
  • Glial Fibrillary Acidic Protein / metabolism
  • Mice
  • Mice, Inbred ICR
  • Pregnancy
  • Prenatal Exposure Delayed Effects / physiopathology*
  • Receptors, Glucocorticoid / metabolism
  • Reflex / physiology
  • Sucrose / administration & dosage
  • Swimming / psychology

Substances

  • Glial Fibrillary Acidic Protein
  • Receptors, Glucocorticoid
  • Sucrose
  • Bromodeoxyuridine
  • Corticosterone