首页> 美国卫生研究院文献>Iranian Journal of Basic Medical Sciences >Mouse Oocytes and Embryos Cryotop-vitrification Using Low Concentrated Solutions: Effects on Meiotic Spindle Genetic Material Array and Developmental Ability
【2h】

Mouse Oocytes and Embryos Cryotop-vitrification Using Low Concentrated Solutions: Effects on Meiotic Spindle Genetic Material Array and Developmental Ability

机译:使用低浓度溶液的小鼠卵母细胞和胚胎冷冻玻璃化:对减数分裂纺锤体遗传材料阵列和发育能力的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Objective(s): The examination of the possibility of applying lower CPA- concentrations and obtaining the similar results to those using higher concentrations; as it is shown, the toxicity of the CPAs used in vitrification approach will diminish. >Materials and Methods: Following vitrification/warming, oocytes were subjected to PZD/ICSI. SRs, FRs, and DRs were recorded. SRs and DRs of the embryos were monitored after vitrification/warming. IHC studies were done. Data were analyzed in comparison to the data of Exp. (experimental groups) applying 1.5 M CPA- concentrations (largely-used concentration). >Results: The data of oocytes exposed to 1.25 M concentrated CPAs were in consistency with those exposed to 1.5 M and fresh oocytes in terms of SRs, FRs and DRs. Normal spindle and chromatin configuration is in consistence between the two experimental groups, but lower in comparison with control group. The lower the concentrations were, the less SRs, FRs, DRs were. Also, spindle organizations were more normal in comparison with the experimental groups as the concentrations decreased. The results of DRs for embryos which were exposed to 1.25 and 1.0 M concentrated CPAs were close to those vitrified with 1.5 M and fresh embryos but IHC observations in the three Exp. were significantly lower than those of fresh embryos. The results of 7.5 M concentrated CPAs solutions were significantly lower than those of the control group 1.5, 1.25 and 1.0 M treated. >Conclusions: Vitrification by cryotop technology using minimal volume approach increases both cooling and warming rates, therefore, the CPAs limited reduction to 1.25 and 1.0 M instead of using 1.5 M for oocytes and embryos cryotop-vitrification procedure, may be a slight adjustment.
机译:>目标:检查使用较低CPA-浓度并获得与使用较高CPA-浓度相似的结果的可能性;如图所示,用于玻璃化方法的CPA的毒性将降低。 >材料和方法:玻璃化/加热后,对卵母细胞进行PZD / ICSI。记录了SR,FR和DR。玻璃化/加热后,监测胚胎的SR和DR。 IHC研究已经完成。将数据与Exp。的数据进行比较。 (实验组)应用1.5 M CPA-浓度(常用浓度)。 >结果:在SR,FR和DR方面,暴露于1.25 M浓缩CPA的卵母细胞的数据与暴露于1.5 M和新鲜卵母细胞的卵母细胞的数据一致。两个实验组之间的纺锤体和染色质构型正常,但与对照组相比较低。浓度越低,SR,FR,DR越少。另外,随着浓度的降低,纺锤体组织与实验组相比更为正常。暴露于1.25和1.0 M浓缩CPA的胚胎的DR结果接近于用1.5 M和新鲜胚胎玻璃化的胚胎的DR结果,但是在三个Exp中观察到IHC。明显低于新鲜胚胎。 7.5 M浓缩CPAs溶液的结果显着低于对照组1.5、1.25和1.0 M处理的结果。 >结论:采用最小体积方法通过冷冻顶技术进行玻璃化会增加冷却和升温速率,因此,将CPA限制在1.25和1.0 M,而不是将卵母细胞和胚胎冷冻玻璃化过程使用1.5 M降低稍作调整。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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