[Regulation of oocyte meiotic resumption in mammals]

Fiziol Zh (1994). 2012;58(6):89-97.
[Article in Ukrainian]

Abstract

Currently, the molecular mechanisms involved in induction of oocyte meiotic resumption in the pre-ovulatory follicle which may include (involve) the elimination of meiosis inhibiting factors and/or the accumulation or activation of oocyte maturation signals are actively studied. The present review summarizes the existing literature data regarding the participation of cyclic monophosphates (cAMP and cGMP), protein kinases (mitogen-activated protein kinase (MAPK), AI, AII, B, C, G), epidermal-growth factors (EGF), EGF-like factors, mRNA EGF and EGF-like factors, ovarian steroid hormones and sterols, as well as transcription factors NF-kappaB and CREB (cAMP response element binding protein) in the regulation of mammalian oocyte meiotic resumption. Such scheme of regulation of oocyte meiotic resumption is discussed (considered): the action ofgonadotrophins, FSH and LH, causes increase the production ofcAMP and subsequent activation of MAPK. cGMP (during follicular growth) can prevent untimely oocyte meiotic resumption up to ovulation (after LH surge, after increase in LH). FSH- and the LH -induced system of EGF, steroids and sterols are involved in MAPK activation. Whereas different FSH and LH effects on NO production in ovary are involved in the regulation of induction of oocyte meiotic resumption in mammals. The further research is needed to better understand the new important mechanisms that regulate difficult aspects of oocyte meiotic maturation in mammals.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Animals
  • Cyclic AMP Response Element-Binding Protein / genetics
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Epidermal Growth Factor / genetics
  • Epidermal Growth Factor / metabolism
  • Female
  • Follicle Stimulating Hormone / genetics
  • Follicle Stimulating Hormone / metabolism
  • Gene Expression Regulation, Developmental*
  • Luteinizing Hormone / genetics
  • Luteinizing Hormone / metabolism
  • Mammals
  • Meiosis / genetics*
  • Mitogen-Activated Protein Kinases / genetics
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Nucleotides, Cyclic / metabolism
  • Oocytes / cytology
  • Oocytes / growth & development*
  • Oogenesis / genetics*
  • Ovarian Follicle / cytology
  • Ovarian Follicle / growth & development*
  • Ovulation / genetics

Substances

  • Cyclic AMP Response Element-Binding Protein
  • NF-kappa B
  • Nucleotides, Cyclic
  • Epidermal Growth Factor
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • Mitogen-Activated Protein Kinases