Sharjah Equine Hospital, Sharjah, UAE.
Equine Vet J. 2021 Nov;53(6):1227-1233. doi: 10.1111/evj.13400. Epub 2021 Jan 11.
Successful vitrification of equine expanded blastocysts requires collapse of the blastocoele cavity using a micromanipulator-mounted biopsy pipette on an inverted microscope. Such equipment is expensive and requires user skill.
To develop a manual method of blastocoele collapse prior to vitrification using commercial products.
In vivo experiment.
Seventy-nine Day 7 or 8 embryos were measured and graded. Twenty were vitrified following micromanipulator-assisted puncture and aspiration before being used to validate commercial human vitrification and warming kits containing, respectively, 2-step concentrations of DMSO and ethylene glycol (7.5%-15% v:v) and decreasing concentrations of sucrose. After warming, embryos were transferred to recipient mares. Once validated, the commercial kits were used to vitrify and warm a further 39 embryos which were punctured manually using a microneedle, 2 (5%) were damaged during puncture and excluded; 20 more embryos were vitrified without puncture. Embryos were grouped as follows: non-punctured ≤ 300µm (n = 10) and >300 to ≤560 µm (n = 10), punctured small (>300 to ≤560 µm; n = 17) and large (>560 µm; n = 10) and exposed to the equilibration solution (ES) in the kit for 6min. An additional group of punctured large embryos was exposed to ES for 8min (n = 10). For the initial warming step, embryos were exposed for 1min to the thawing solution at 42°C, before being moved to a dilution solution at room temperature.
Vitrified, manually punctured embryos ≤560 µm exposed to ES for 6min resulted in a pregnancy rate of 82% (14/17). Unpunctured embryos ≤300 µm gave an 80% (8/10) pregnancy rate. Larger unpunctured embryos, punctured embryos >560 µm and embryos exposed to ES for 8min gave significantly reduced pregnancy rates.
Limited group sizes.
High pregnancy rates can be achieved by manually puncturing ≤560 µm equine embryos prior to their vitrification and subsequent warming in commercial media.
成功的马属动物扩展囊胚玻璃化需要使用倒置显微镜上安装的微操作仪活检管来塌陷囊胚腔。这种设备昂贵且需要用户具备一定的技能。
开发一种使用商业产品在玻璃化前手动塌陷囊胚腔的方法。
体内实验。
对 79 枚第 7 天或第 8 天的胚胎进行测量和分级。20 枚胚胎在经过微操作辅助穿刺和抽吸后进行玻璃化处理,然后用于验证含有分别为 2 步浓度的二甲基亚砜和乙二醇(7.5%-15% v:v)以及浓度逐渐降低的蔗糖的商业人类玻璃化和升温试剂盒。在升温后,胚胎被转移到受体母马体内。一旦经过验证,商业试剂盒就用于玻璃化和升温另外 39 枚胚胎,这些胚胎使用微针手动穿刺,2 枚(5%)在穿刺过程中受损并被排除;另外 20 枚胚胎未穿刺。胚胎分为以下几组:未穿刺≤300µm(n=10)和>300 至≤560µm(n=10),穿刺小(>300 至≤560µm;n=17)和大(>560µm;n=10),并暴露于试剂盒中的平衡溶液(ES)中 6 分钟。另外一组穿刺的大胚胎暴露于 ES 中 8 分钟(n=10)。对于初始升温步骤,胚胎在 42°C 的解冻溶液中暴露 1 分钟,然后转移到室温下的稀释溶液中。
在 ES 中暴露 6 分钟的玻璃化、手动穿刺的≤560µm 胚胎的妊娠率为 82%(14/17)。未穿刺的≤300µm 胚胎的妊娠率为 80%(8/10)。未穿刺的较大胚胎、穿刺的>560µm 胚胎和暴露于 ES 8 分钟的胚胎的妊娠率显著降低。
有限的组大小。
通过在商业培养基中手动穿刺≤560µm 的马属动物胚胎并随后进行玻璃化和升温,可以获得较高的妊娠率。