N-acetyl-L-cysteine Improves the Developmental Competence of Bovine Oocytes and Embryos Cultured In Vitro by Attenuating Oxidative Damage and Apoptosis.
Wu-Sheng SunHoon JangMi-Ryung ParkKeon Bong OhHaesun LeeSeong-Soo HwangLi-Jie XuIn-Sul HwangJeong-Woong LeePublished in: Antioxidants (Basel, Switzerland) (2021)
Oxidative stress has been suggested to negatively affect oocyte and embryo quality and developmental competence, resulting in failure to reach full term. In this study, we investigated the effect of N-acetyl-L-cysteine (NAC), a cell-permeating antioxidant, on developmental competence and the quality of oocytes and embryos upon supplementation (0.1-10 mM) in maturation and culture medium in vitro using slaughterhouse-derived oocytes and embryos. The results show that treating oocytes with 1.0 mM NAC for 8 h during in vitro maturation attenuated the intracellular reactive oxygen species (ROS) (p < 0.05) and upregulated intracellular glutathione levels (p < 0.01) in oocytes. Interestingly, we found that NAC affects early embryonic development, not only in a dose-dependent, but also in a stage-specific, manner. Significantly (p < 0.05) decreased cleavage rates (90.25% vs. 81.46%) were observed during the early stage (days 0-2), while significantly (p < 0.05) increased developmental rates (38.20% vs. 44.46%) were observed during the later stage (from day 3) of embryonic development. In particular, NAC supplementation decreased the proportion of apoptotic blastomeres significantly (p < 0.05), resulting in enhanced hatching capability and developmental rates during the in vitro culture of embryos. Taken together, our results suggest that NAC supplementation has beneficial effects on bovine oocytes and embryos through the prevention of apoptosis and the elimination of oxygen free radicals during maturation and culture in vitro.
Keyphrases
- oxidative stress
- transcription factor
- reactive oxygen species
- cell death
- early stage
- dna damage
- genome wide analysis
- endoplasmic reticulum stress
- cell cycle arrest
- preterm infants
- endothelial cells
- anti inflammatory
- ischemia reperfusion injury
- stem cells
- mesenchymal stem cells
- quality improvement
- signaling pathway
- cell proliferation
- high resolution
- neoadjuvant chemotherapy
- gestational age
- preterm birth