FSH signaling is involved in affective disorders

Biochem Biophys Res Commun. 2020 May 14;525(4):915-920. doi: 10.1016/j.bbrc.2020.03.039. Epub 2020 Mar 11.

Abstract

Affective disorders are a set of mental disorders and particularly disrupt the mental health of susceptible women during puberty, pregnancy, parturition and menopause transition, which are characterized by dramatic changes in reproductive hormone profiles. The serum FSH level changes significantly during these periods; yet, the role of FSH in mood regulation is poorly understood. In the current study, FSHR knockout (Fshr-/-) mice displayed enhanced affective disorder behaviors in an open field test and a forced swim test, accompanied by altered gene expression profiles. The differentially expressed genes between Fshr-/- mice and Fshr+/+ mice were enriched in multiple neuroendocrine metabolic pathways. FSHR deletion significantly increased/decreased the mRNA and/or protein expression levels of AOX1, RDH12, HTR3a and HTR4 in mood-mediating brain regions, including the hippocampus and prefrontal cortex. These results reveal that FSH signaling is involved in the development of affective disorders.

Keywords: Affective disorders; Anxiety; Depression; FSH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Oxidoreductases / genetics
  • Alcohol Oxidoreductases / metabolism
  • Aldehyde Oxidase / genetics
  • Aldehyde Oxidase / metabolism
  • Animals
  • Behavior, Animal
  • Female
  • Follicle Stimulating Hormone / metabolism*
  • Hippocampus / physiology*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mood Disorders / genetics
  • Mood Disorders / metabolism*
  • Prefrontal Cortex / physiology*
  • Receptors, FSH / genetics
  • Receptors, FSH / metabolism*
  • Receptors, Serotonin, 5-HT3 / genetics
  • Receptors, Serotonin, 5-HT3 / metabolism
  • Signal Transduction
  • Transcriptome

Substances

  • Htr3a protein, mouse
  • Receptors, FSH
  • Receptors, Serotonin, 5-HT3
  • Follicle Stimulating Hormone
  • Alcohol Oxidoreductases
  • Rdh12 protein, mouse
  • Aldehyde Oxidase
  • Aox1 protein, mouse