Antidepressant effects of esketamine via the BDNF/AKT/mTOR pathway in mice with postpartum depression and their offspring

Prog Neuropsychopharmacol Biol Psychiatry. 2024 Jun 8:132:110992. doi: 10.1016/j.pnpbp.2024.110992. Epub 2024 Mar 13.

Abstract

Postpartum depression (PPD) is a serious mental health problem that can negatively affect future generations. BDNF/AKT/mTOR signaling in the frontal lobe and hippocampus in mice is associated with depression, but its role in mice with PPD and their offspring is unknown. This study was aimed at investigating the effects of esketamine (ESK), a drug approved for treatment of refractory depression, on the BDNF/AKT/mTOR pathway in mice with PPD and their offspring. A model of chronic unpredictable mild stress with pregnancy was used. ESK was injected into postpartum mice, and behavioral tests were conducted to predict the severity of symptoms at the end of lactation and in the offspring after adulthood. Both mice with PPD and their offspring showed significant anxiety- and depression-like behaviors that were ameliorated with the ESK intervention. ESK enhanced exploratory behavior in unfamiliar environments, increased the preference for sucrose, and ameliorated the impaired BDNF/AKT/mTOR signaling in the frontal and hippocampal regions in mice. Thus, ESK may have great potential in treating PPD and decreasing the incidence of depression in offspring.

Keywords: BDNF/AKT/mTOR; Esketamine; Postpartum depression.

MeSH terms

  • Animals
  • Antidepressive Agents / metabolism
  • Antidepressive Agents / pharmacology
  • Antidepressive Agents / therapeutic use
  • Brain-Derived Neurotrophic Factor / metabolism
  • Depression / psychology
  • Depression, Postpartum* / drug therapy
  • Depression, Postpartum* / metabolism
  • Disease Models, Animal
  • Female
  • Hippocampus / metabolism
  • Ketamine*
  • Mice
  • Pregnancy
  • Proto-Oncogene Proteins c-akt / metabolism
  • Stress, Psychological / drug therapy
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Antidepressive Agents
  • Brain-Derived Neurotrophic Factor
  • Esketamine
  • Ketamine
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases