Chlorogenic acid improves the development of porcine parthenogenetic embryos by regulating oxidative stress and ameliorating mitochondrial function

Reprod Domest Anim. 2024 May;59(5):e14596. doi: 10.1111/rda.14596.

Abstract

Chlorogenic acid (CGA) is an effective phenolic antioxidant that can scavenge hydroxyl radicals and superoxide anions. Herein, the protective effects and mechanisms leading to CGA-induced porcine parthenogenetic activation (PA) in early-stage embryos were investigated. Our results showed that 50 μM CGA treatment during the in vitro culture (IVC) period significantly increased the cleavage and blastocyst formation rates and improved the blastocyst quality of porcine early-stage embryos derived from PAs. Then, genes related to zygotic genome activation (ZGA) were identified and investigated, revealing that CGA can promote ZGA in porcine PA early-stage embryos. Further analysis revealed that CGA treatment during the IVC period decreased the abundance of reactive oxygen species (ROS), increased the abundance of glutathione and enhanced the activity of catalase and superoxide dismutase in porcine PA early-stage embryos. Mitochondrial function analysis revealed that CGA increased mitochondrial membrane potential and ATP levels and upregulated the mitochondrial homeostasis-related gene NRF-1 in porcine PA early-stage embryos. In summary, our results suggest that CGA treatment during the IVC period helps porcine PA early-stage embryos by regulating oxidative stress and improving mitochondrial function.

Keywords: chlorogenic acid; mitochondrial function; oxidative stress; parthenogenetic embryo; porcine.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Blastocyst / drug effects
  • Chlorogenic Acid* / pharmacology
  • Embryo Culture Techniques* / veterinary
  • Embryonic Development* / drug effects
  • Female
  • Glutathione / metabolism
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria* / drug effects
  • Oxidative Stress* / drug effects
  • Parthenogenesis* / drug effects
  • Reactive Oxygen Species* / metabolism
  • Swine

Associated data

  • RefSeq/NW_018085108.1
  • RefSeq/XM_003358822.4
  • RefSeq/XM_021097584.1
  • RefSeq/NM_001032355.1
  • RefSeq/NM_001293163.2