CUMS Promotes the Development of Premature Ovarian Insufficiency Mediated by Nerve Growth Factor and Its Receptor in Rats

Biomed Res Int. 2020 Jun 30:2020:1946853. doi: 10.1155/2020/1946853. eCollection 2020.

Abstract

This study aimed to investigate whether chronic unpredictable mild stress (CUMS) affects follicular development in ovaries through the nerve growth factor (NGF)/high affinity nerve growth factor receptor, the Tropomyosin-related kinase A (TrkA) receptor, mediated signaling pathway and to reveal the relationship between chronic stress and premature ovarian insufficiency (POI) development. In this experiment, a CUMS rat model was constructed. It was found that serum estradiol (E2), anti-Mullerian hormone (AMH), and gonadotropin-releasing hormone (GnRH) levels decreased, while follicle-stimulating hormone (FSH) levels increased. The expression of NGF, TrkA, p75, and FSHR in ovarian tissue decreased significantly. The expression levels of TrkA and p75 protein in ovarian stroma and small follicles were observed by an immunofluorescence assay. In addition, the numbers of small follicles were significantly reduced. The expression of TrkA, p75, and FSHR in CUMS ovarian tissue was upregulated by exogenous NGF in vitro. Furthermore, after treatment with NGF combined with FSH, E2 secretion in ovarian tissue culture supernatant of CUMS rats also increased significantly. Therefore, CUMS downregulates NGF and TrkA and promotes the occurrence of POI in rats. Exogenous NGF and FSH can upregulate the NGF receptor, E2, and AMH in vitro, and improve the rat ovarian function. Future studies may associate these results with female population.

MeSH terms

  • Animals
  • Anti-Mullerian Hormone / blood
  • Estradiol / blood
  • Female
  • Follicle Stimulating Hormone / blood
  • Gonadotropin-Releasing Hormone / blood
  • Humans
  • Nerve Growth Factor / metabolism*
  • Ovarian Follicle / metabolism
  • Ovarian Follicle / pathology
  • Primary Ovarian Insufficiency / blood
  • Primary Ovarian Insufficiency / genetics
  • Primary Ovarian Insufficiency / psychology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley
  • Receptor, Nerve Growth Factor / metabolism*
  • Receptor, trkA / genetics
  • Receptor, trkA / metabolism
  • Receptors, FSH / genetics
  • Receptors, FSH / metabolism
  • Stress, Psychological / blood
  • Stress, Psychological / complications*
  • Up-Regulation / genetics

Substances

  • RNA, Messenger
  • Receptor, Nerve Growth Factor
  • Receptors, FSH
  • Gonadotropin-Releasing Hormone
  • Estradiol
  • Anti-Mullerian Hormone
  • Follicle Stimulating Hormone
  • Nerve Growth Factor
  • Receptor, trkA