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通过一步添加乙二醇对体外生产的牛胚胎进行玻璃化处理。

Vitrification of in vitro-produced bovine embryos by addition of ethylene glycol in one-step.

作者信息

Walker D J, Campos-Chillon L F, Seidel G E

机构信息

Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, CO, USA.

出版信息

Reprod Domest Anim. 2006 Oct;41(5):467-71. doi: 10.1111/j.1439-0531.2006.00699.x.

Abstract

The objective of this study was to simplify two-step addition of cryoprotectant for vitrification of bovine embryos by developing a one-step procedure. Survival was calculated as a percentage of non-vitrified controls developed from the same batch of oocytes. In experiment 1, bovine blastocysts were vitrified following one- or two-step addition of cryoprotectant. Exposure of embryos to cryoprotectant in one-step resulted in survival rates not significantly lower (p > 0.1) than those obtained by two-step addition (85% vs 98%, respectively). Based on these results, experiments 2-4 were designed to test one-step addition of cryoprotectant more rigorously. Experiment 2 exposed day 7 blastocysts to 6, 7 or 8 M ethylene glycol for 2.5 or 3.5 min. At 24 h post-vitrification, survival of embryos was similar, irrespective of ethylene glycol concentration or exposure time (6 M 38%, 7 M 51%, 8 M 59%; 2.5 min 54%, 3.5 min 45%). In experiment 3, blastocysts were exposed to 7 M ethylene glycol for shorter times (30 or 60 s); 30 s exposure resulted in decreased survival (8% vs 31%, p < 0.05). Experiment 4 concerned one-step addition of cryoprotectant to day 6 bovine morulae, exposed to 7 M ethylene glycol for 1 or 1.5 min. There was no difference in survival between exposure times of 1 or 1.5 min (28% vs 45%, respectively; p > 0.1). It is unclear why many embryos survive vitrification with one-step addition of cryoprotectant, but others do not. Although, one-step addition of cryoprotectant simplifies the vitrification procedure, survival rates were inadequate for routine cryopreservation of in vitro-produced bovine embryos.

摘要

本研究的目的是通过开发一种一步法程序来简化用于牛胚胎玻璃化的两步添加冷冻保护剂的方法。存活率以同一批卵母细胞发育而来的未玻璃化对照的百分比来计算。在实验1中,牛囊胚在一步或两步添加冷冻保护剂后进行玻璃化。一步将胚胎暴露于冷冻保护剂中导致的存活率与两步添加法获得的存活率相比无显著降低(p>0.1)(分别为85%和98%)。基于这些结果,设计实验2 - 4更严格地测试一步添加冷冻保护剂的方法。实验2将第7天的囊胚暴露于6 M、7 M或8 M乙二醇中2.5或3.5分钟。玻璃化后24小时,无论乙二醇浓度或暴露时间如何,胚胎的存活率相似(6 M为38%,7 M为51%,8 M为59%;2.5分钟为54%,3.5分钟为45%)。在实验3中,囊胚暴露于7 M乙二醇的时间更短(30或60秒);30秒的暴露导致存活率降低(8%对31%,p<0.05)。实验4涉及对第6天的牛桑椹胚一步添加冷冻保护剂,将其暴露于7 M乙二醇中1或1.5分钟。1或1.5分钟的暴露时间之间存活率无差异(分别为28%和45%;p>0.1)。目前尚不清楚为什么许多胚胎通过一步添加冷冻保护剂能在玻璃化中存活,而其他胚胎则不能。尽管一步添加冷冻保护剂简化了玻璃化程序,但存活率对于体外生产的牛胚胎的常规冷冻保存来说仍不足够。

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