Effect of Kisspeptin on the Developmental Competence and Early Transcript Expression in Porcine Oocytes Parthenogenetically Activated with Different Methods

Biomed Res Int. 2018 Feb 21:2018:3693602. doi: 10.1155/2018/3693602. eCollection 2018.

Abstract

Recent studies showed the modulatory effect of kisspeptin (KP) on calcium waves through the cell membrane and inside the cell. Spermatozoon can induce similar ooplasmic calcium oscillations at fertilization to trigger meiosis II. Here, we evaluated the effect of KP supplementation with 6-dimethylaminopurine (6-DMAP) for 4 h on embryonic development after oocyte activation with single electric pulse, 5 µM ionomycin, or 8% ethanol. Compared to control nonsupplemented groups, KP significantly improved embryo developmental competence electric- and ethanol-activated oocytes in terms of cleavage (75.3% and 58.6% versus 64% and 48%, respectively, p < 0.05) and blastocyst development (31.3% and 10% versus 19.3% and 4%, respectively, p < 0.05). MOS expression was increased in electrically activated oocytes in presence of KP while it significantly reduced CCNB1 expression. In ionomycin treated group, both MOS and CCNB1 showed significant increase with no difference between KP and control groups. In ethanol-treated group, KP significantly reduced CCNB1 but no effect was observed on MOS expression. The early alterations in MOS and CCNB1 mRNA transcripts caused by KP may explain the significant differences in the developmental competence between the experimental groups. Kisspeptin supplementation may be adopted in protocols for porcine oocyte activation through electric current and ethanol to improve embryonic developmental competence.

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / pharmacology
  • Animals
  • Blastocyst / drug effects
  • Blastocyst / metabolism
  • Cyclin B1 / metabolism
  • Embryonic Development / drug effects
  • Embryonic Development / physiology
  • Ionomycin / pharmacology
  • Kisspeptins / metabolism*
  • Oncogene Proteins v-mos / metabolism
  • Oocytes / drug effects
  • Oocytes / metabolism*
  • Parthenogenesis / drug effects
  • Parthenogenesis / physiology*
  • RNA, Messenger / metabolism
  • Swine

Substances

  • Cyclin B1
  • Kisspeptins
  • Oncogene Proteins v-mos
  • RNA, Messenger
  • Ionomycin
  • N(6),N(6)-dimethyladenine
  • Adenine