首页> 外文期刊>Theriogenology >Holding bovine oocytes in the absence of maturation inhibitors: Kinetics of in vitro maturation and effect on blastocyst development after in vitro fertilization.
【24h】

Holding bovine oocytes in the absence of maturation inhibitors: Kinetics of in vitro maturation and effect on blastocyst development after in vitro fertilization.

机译:在没有成熟抑制剂的情况下保持牛卵母细胞:体外成熟的动力学以及体外受精后对胚泡发育的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

Holding immature oocytes before maturation simplifies the transport of oocytes and aids in scheduling later manipulations. We examined the effect of holding bovine oocytes in the absence of meiotic inhibitors on their subsequent meiotic and developmental competence. Oocytes were matured immediately after recovery (control) or were held in a mixture of 40% TCM 199 with Earle's salts, 40% TCM 199 with Hanks' salts, and 20% FBS, at room temperature for 16 to 18h (EH-held) and then matured. Chromatin status was determined at 0, 10, 14, 18, and 22h of maturation culture. Oocytes were fertilized in vitro after either 18 or 22-24h maturation. The EH treatment maintained oocytes at the germinal vesicle stage (79.3%, vs. 87.7% for control oocytes at 0h; P>0.05). Upon culture, held oocytes matured more quickly than did control oocytes. The proportions of mature oocytes were not significantly different between groups at 18h (EH-held, 80.6% and control, 79.3%); however, after 22h significantly more EH-held than control oocytes had degenerated (24.1% vs. 4.5%, P<0.0001). Blastocyst development was similar between groups for oocytes fertilized after 18h maturation (EH-held, 29.6% and control, 27.8%). When oocytes were fertilized after 22-24h maturation, EH-held oocytes yielded lower blastocyst development than did control oocytes (16.5% vs. 29.3%, P<0.05). In conclusion, bovine oocytes may be effectively held in the EH treatment before maturation without adversely affecting meiotic or developmental competence. However, holding affects the kinetics of maturation and this must be taken into account when subsequent manipulations are performed.
机译:在成熟之前持有未成熟的卵母细胞可以简化卵母细胞的运输,并有助于安排以后的操作。我们研究了在不存在减数分裂抑制剂的情况下保持牛卵母细胞对其随后的减数分裂和发育能力的影响。卵母细胞恢复后立即成熟(对照)或在室温下于40%TCM 199与Earle盐,40%TCM 199与Hanks's盐和20%FBS的混合物中保持16至18h(EH保持)然后成熟。在成熟培养的0、10、14、18和22h确定染色质状态。 18或22-24小时成熟后,卵母细胞体外受精。 EH处理使卵母细胞保持在生小泡阶段(79.3%,而对照卵母细胞在0h时为87.7%; P> 0.05)。培养后,保持的卵母细胞比对照卵母细胞成熟更快。两组在18h时成熟卵母细胞的比例无显着差异(EH级为80.6%,对照组为79.3%)。然而,在22小时后,持有的EH明显比对照卵母细胞退化的多(24.1%对4.5%,P <0.0001)。卵囊成熟后18h,受精卵组之间的囊胚发育相似(EH保持为29.6%,对照为27.8%)。当卵母细胞在成熟后22-24h受精后,与对照卵母细胞相比,持EH卵母细胞的胚泡发育率更低(16.5%对29.3%,P <0.05)。总之,牛卵母细胞可以在成熟前有效地保持在EH治疗中,而不会对减数分裂或发育能力产生不利影响。但是,保持会影响成熟的动力学,因此在执行后续操作时必须考虑到这一点。

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