The antioxidant dieckol reduces damage of oxidative stress-exposed porcine oocytes and enhances subsequent parthenotes embryo development

Mol Reprod Dev. 2021 May;88(5):349-361. doi: 10.1002/mrd.23466. Epub 2021 Apr 12.

Abstract

This study investigated the effect of the antioxidant dieckol, a component of Ecklonia cava, on maturation and developmental competence of porcine oocytes exposed to oxidative stress in vitro. Oocytes were matured in in vitro maturation (IVM) medium containing various concentrations of dieckol. The blastocyst formation rate was highest in the 0.5 μM dieckol-treated (0.5 DEK) group. The reactive oxygen species level was decreased, and the level of glutathione and expression of antioxidant genes (NFE2L, SOD1, and SOD2) at metaphase II were increased in the 0.5 DEK group. Abnormal spindle organization and chromosome misalignment were prevented in the 0.5 DEK group. Expression of maternal markers (CCNB1 and MOS) and activity of p44/42 mitogen-activated protein kinase were increased in the 0.5 DEK group. After parthenogenetic activation, the total number of cells per blastocyst was increased and the percentage of apoptotic cells was decreased in the 0.5 DEK group. Expression of development-related genes (CX45, CDX2, POU5F1, and NANOG), antiapoptotic genes (BCL2L1 and BIRC5), and a proapoptotic gene (CASP3) were altered in the 0.5 DEK group. These results indicate that the antioxidant dieckol improves IVM and subsequent development of porcine oocytes and can be used to improve the quality of oocytes under peroxidation experimental conditions.

Keywords: IVM; dieckol; embryo; oxidative stress; porcine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / administration & dosage
  • Antioxidants / pharmacology*
  • Benzofurans / administration & dosage
  • Benzofurans / pharmacology*
  • Blastocyst / cytology
  • Chromosome Positioning / drug effects
  • Dose-Response Relationship, Drug
  • Embryo Culture Techniques
  • Embryonic Development / drug effects*
  • Female
  • Gene Expression Regulation, Developmental / drug effects
  • Glutathione / metabolism
  • In Vitro Oocyte Maturation Techniques
  • MAP Kinase Signaling System / drug effects
  • Meiosis
  • Oocytes / drug effects*
  • Oocytes / metabolism
  • Oxidative Stress / drug effects*
  • Parthenogenesis / drug effects*
  • Phaeophyceae / chemistry
  • Reactive Oxygen Species / metabolism
  • Spindle Apparatus / drug effects
  • Spindle Apparatus / ultrastructure
  • Swine

Substances

  • Antioxidants
  • Benzofurans
  • Reactive Oxygen Species
  • dieckol
  • Glutathione