...
首页> 外文期刊>Journal of reproduction and fertility >Differences in pronucleus formation and first cleavage following in vitro fertilization between pig oocytes matured in vivo and in vitro
【24h】

Differences in pronucleus formation and first cleavage following in vitro fertilization between pig oocytes matured in vivo and in vitro

机译:体内和体外成熟的猪卵母细胞体外受精后原核形成和首次卵裂的差异

获取原文
           

摘要

To elucidate the developmental differences occurring after in vitro fertilization (IVF) of pig oocytes matured either in vitro (n = 1934) or in vivo (n = 1128), the present experiment investigated the morphological changes from penetration to the two-cell stage. Oocytes were examined every 2–4 h from 2 to 32 h after in vitro insemination to study sperm penetration, male and female pronucleus formation, synkaryosis and first cleavage. The penetration rate was significantly higher (P < 0.05) for in vivo matured oocytes (69.8%) than for in vitro matured oocytes (35.0%). Penetration of spermatozoa into the ooplasm was first recorded 6 h (in vitro matured oocytes) and 4 h (in vivo matured oocytes) after addition of the spermatozoa to the oocytes. For both in vivo and in vitro matured oocytes, 2 h were required for sperm head decondensation. However, maximum sperm head decondensation occurred 2 h later in in vitro matured oocytes. Within 6 h, 41.7 ± 5.6% of the in vivo matured oocytes had completed second meiotic division, whereas only 20.8 ± 6.5% of the in vitro matured oocytes reached this developmental stage (P < 0.01). For in vitro matured oocytes, male pronucleus formation was retarded 2–4 h after onset of insemination and development of the female pronucleus was enhanced compared with in vivo matured oocytes. Synchronized opposing pronuclei were observed 14 h after insemination in in vitro matured oocytes and after 8 h in in vivo matured oocytes. Synkaryosis was first observed at 16 and 18 h in in vivo and in vitro matured oocytes, respectively. First cleavage was observed 32 h (in vitro matured oocytes) and 28 h (in vivo matured oocytes) after insemination. It is concluded that under our IVF conditions, oocytes matured in vitro display lower penetration and cleavage rates and asynchronous pronucleus development, as well as delayed cleavage, compared with oocytes matured in vivo.
机译:为了阐明在体外受精(IVF)的猪卵母细胞在体外(n = 1934)或体内(n = 1128)成熟后发生的发育差异,本实验研究了从穿透到两细胞阶段的形态变化。体外受精后2至32小时,每2-4小时检查一次卵母细胞,以研究精子渗透,雄性和雌性前核形成,突触形成和第一次卵裂。体内成熟的卵母细胞(69.8%)的穿透率显着高于体外成熟的卵母细胞(35.0%)的穿透率(P <0.05)。在将精子添加到卵母细胞中之后,首先记录6小时(体外成熟的卵母细胞)和4小时(体内成熟的卵母细胞)中的精子穿透。对于体内和体外成熟的卵母细胞,精子头去凝需要2小时。但是,在体外成熟卵母细胞中,最大的精子头冷凝发生在2小时后。在6小时内,体内成熟卵母细胞的41.7±5.6%完成了第二次减数分裂,而体外成熟卵母细胞中只有20.8±6.5%达到了这个发育阶段(P <0.01)。对于体外成熟的卵母细胞,与体内成熟的卵母细胞相比,在授精开始后2-4小时,男性原核的形成被延迟,女性原核的发育得以增强。在体外成熟卵母细胞受精后14小时,在体内成熟卵母细胞8小时后,观察到同步的相反核。首先在体内和体外成熟卵母细胞中分别在16和18 h观察到突触形成。授精后32小时(体外成熟的卵母细胞)和28小时(体内成熟的卵母细胞)观察到第一次切割。结论是,在体外受精的条件下,与体内成熟的卵母细胞相比,体外成熟的卵母细胞显示出较低的穿透率和卵裂率,异步原核发育以及延迟的卵裂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号