Whitaker B D, Casey S J, Taupier R
Department of Agriculture, Ferrum College, Ferrum, VA 24088, USA.
Reprod Fertil Dev. 2012;24(8):1048-54. doi: 10.1071/RD12002.
The effects of supplementation with 1.5 mM n-acetyl-l-cysteine (NAC) during in vitro oocyte maturation were studied. Oocytes were supplemented with 1.5 mM NAC during maturation for 0 to 24 h, 24 to 48 h, or 0 to 48 h then subjected to IVF and embryo development. Oocytes were evaluated after maturation for intracellular glutathione concentration, superoxide dismutase and glutathione peroxidase activities and DNA fragmentation. Fertilisation and embryonic development success were also evaluated. There was no effect of treatment on intracellular glutathione concentrations, enzyme activities or fertilisation success rates. Supplementing NAC during maturation significantly decreased (P < 0.05) the percentage of oocytes with fragmented DNA compared with no NAC supplementation. Supplementing NAC from 24 to 48 h or 0 to 48 h resulted in a significantly higher (P < 0.05) percentage of oocytes with male pronuclei than for oocytes from the other treatment groups. There was no difference in the percentage of embryos cleaved by 48 h after IVF between treatment groups. Supplementing NAC from 24 to 48 h or 0 to 48 h resulted in a significantly higher (P < 0.05) percentage of embryos reaching the blastocyst stage by 144 h after IVF compared with the other treatment groups. These results indicate that supplementation of the oocyte maturation medium with 1.5 mM NAC, specifically during the last 24 h, improves male pronucleus formation and blastocyst development in pigs.
研究了在体外卵母细胞成熟过程中添加1.5 mM N-乙酰-L-半胱氨酸(NAC)的效果。卵母细胞在成熟过程中分别在0至24小时、24至48小时或0至48小时添加1.5 mM NAC,然后进行体外受精和胚胎发育。成熟后对卵母细胞进行细胞内谷胱甘肽浓度、超氧化物歧化酶和谷胱甘肽过氧化物酶活性以及DNA片段化评估。还评估了受精和胚胎发育成功率。处理对细胞内谷胱甘肽浓度、酶活性或受精成功率没有影响。与不添加NAC相比,在成熟过程中添加NAC显著降低了(P<0.05)DNA片段化的卵母细胞百分比。在24至48小时或0至48小时添加NAC导致具有雄原核的卵母细胞百分比显著高于(P<0.05)其他处理组的卵母细胞。各处理组在体外受精后48小时卵裂的胚胎百分比没有差异。与其他处理组相比,在24至48小时或0至48小时添加NAC导致在体外受精后144小时达到囊胚阶段的胚胎百分比显著更高(P<0.05)。这些结果表明,在卵母细胞成熟培养基中添加1.5 mM NAC,特别是在最后24小时,可改善猪的雄原核形成和囊胚发育。