Herrid M, Billah M, Skidmore J A
Camel Reproduction Centre, PO Box 79914, Dubai, United Arab Emirates.
Camel Reproduction Centre, PO Box 79914, Dubai, United Arab Emirates.
Anim Reprod Sci. 2017 Dec;187:116-123. doi: 10.1016/j.anireprosci.2017.10.015. Epub 2017 Oct 26.
Successful embryo cryopreservation facilitates the wider application of assisted reproduction technologies and also provides a useful method for gene banking of valuable genetics. Unfortunately attempts to establish an effective cryopreservation protocol for camelid embryos have been unsuccessful. In the current study, a modified vitrification protocol with three steps was investigated, whereby embryos were exposed to solutions containing increasing amounts of glycerol and ethylene glycol for fixed time periods. Embryos were then loaded into an Open Pull Straw (OPS) and plunged directly into liquid nitrogen for storage. Three experiments were designed to investigate the effect of 1) artificial shrinkage (AS) of embryos, 2) the addition of sucrose to the vitrification solutions, and 3) the replacement of sucrose by galactose in the warming solution, on the outcome of vitrification. The results showed that neither AS of hatched embryos prior to vitrification, nor the addition of sucrose into vitrification solutions improves the outcome of vitrification, while replacement of sucrose with galactose in warming solution increases the survival and developmental rates of vitrified embryos in culture. Transfer of vitrified embryos that were warmed in galactose resulted in a pregnancy rate of 42.8% per embryo or 46.1% per recipient. Collectively, these results suggest a possible species-specific toxic effect of sucrose on camel embryos, and that avoiding its use either in vitrification or warming solution is critical for establishing an effective protocol. This study may also be applicable to the vitrification of embryos of other camelid species including alpaca and llamas.
成功的胚胎冷冻保存有助于辅助生殖技术更广泛地应用,同时也为珍贵基因的基因库提供了一种有用的方法。不幸的是,为骆驼科动物胚胎建立有效冷冻保存方案的尝试一直未成功。在本研究中,研究了一种改良的三步玻璃化方案,即让胚胎在固定时间段内暴露于含有递增浓度甘油和乙二醇的溶液中。然后将胚胎装入开放式拉细麦管(OPS),直接投入液氮中保存。设计了三个实验来研究:1)胚胎的人工收缩(AS),2)在玻璃化溶液中添加蔗糖,3)在解冻溶液中用半乳糖替代蔗糖,对玻璃化结果的影响。结果表明,在玻璃化前对孵化胚胎进行AS以及在玻璃化溶液中添加蔗糖均不能改善玻璃化结果,而在解冻溶液中用半乳糖替代蔗糖可提高玻璃化胚胎在培养中的存活率和发育率。在半乳糖中解冻的玻璃化胚胎移植后,每个胚胎的妊娠率为42.8%,每个受体的妊娠率为46.1%。总体而言,这些结果表明蔗糖对骆驼胚胎可能存在物种特异性毒性作用,并且在玻璃化或解冻溶液中避免使用蔗糖对于建立有效方案至关重要。本研究也可能适用于其他骆驼科动物(包括羊驼和美洲驼)胚胎的玻璃化。