Elucidating the Possible Role of FoxO in Depression

Neurochem Res. 2021 Nov;46(11):2761-2775. doi: 10.1007/s11064-021-03364-4. Epub 2021 Jun 1.

Abstract

Forkhead box-O (FoxO) transcriptional factors perform essential functions in several physiological and biological processes. Recent studies have shown that FoxO is implicated in the pathophysiology of depression. Changes in the upstream mediators of FoxOs including brain-derived neurotrophic factor (BDNF) and protein kinase B have been associated with depressive disorder and the antidepressant agents are known to alter the phosphorylation of FoxOs. Moreover, FoxOs might be regulated by serotonin or noradrenaline signaling and the hypothalamic-pituitary-adrenal (HPA)-axis,both of them are associated with the development of the depressive disorder. FoxO also regulates neural morphology, synaptogenesis, and neurogenesis in the hippocampus, which accounts for the pathogenesis of the depressive disorder. The current article underlined the potential functions of FoxOs in the etiology of depressive disorder and formulate few essential proposals for further investigation. The review also proposes that FoxO and its signal pathway might establish possible therapeutic mediators for the management of depressive disorder.

Keywords: Antidepressant agents; Depressive disorder; FoxOs; Synaptogenesis; Transcription factors.

Publication types

  • Review

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology
  • Antidepressive Agents / therapeutic use
  • Brain-Derived Neurotrophic Factor / metabolism
  • Depression / drug therapy
  • Depression / metabolism*
  • Forkhead Box Protein O1 / metabolism
  • Forkhead Transcription Factors / metabolism*
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Humans
  • Hypothalamo-Hypophyseal System / drug effects
  • Hypothalamo-Hypophyseal System / metabolism
  • Norepinephrine / metabolism
  • Pituitary-Adrenal System / drug effects
  • Pituitary-Adrenal System / metabolism
  • Serotonin / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*

Substances

  • Antidepressive Agents
  • Brain-Derived Neurotrophic Factor
  • FOXO1 protein, human
  • Forkhead Box Protein O1
  • Forkhead Transcription Factors
  • Serotonin
  • BDNF protein, human
  • Norepinephrine