Fanelli D, Panzani D, Rota A, Tesi M, Camillo F, Bollwein H, Herrera C
Veterinary Sciences Department, Pisa University, San Piero a Grado, Via Livornese, 56124, Pisa, Italy.
Veterinary Sciences Department, Pisa University, San Piero a Grado, Via Livornese, 56124, Pisa, Italy.
Theriogenology. 2020 Sep 15;154:11-16. doi: 10.1016/j.theriogenology.2020.05.020. Epub 2020 May 16.
Embryo cryopreservation ensures that genetic biodiversity is preserved over time. This study evaluates the survival of donkey embryos subjected to slow freezing and vitrification after thawing and in vitro culture. Seven-day-old in vivo produced donkey embryos were subjected to slow freezing (SF, N = 14) or vitrification (VIT, N = 22). After one year of cryopreservation, embryos were warmed, washed and placed in incubation for in vitro culture (IVC). In order to assess the embryo viability, the quality grade and developmental stage were recorded after thawing and after 24 and 48 h of IVC. Eleven embryos (SF = 4 and VIT = 7) were incubated under a time-lapse camera, for up to 68 h, in order to determine the area and growth. The survival rate was not influenced by the procedure but by the developmental stage: after 48 h of IVC blastocyst survival rate (1/8, 12.5%) was significantly lower compared to both morulas (8/12, 66.7%) and early blastocysts (11/16, 68.7%) (P < 0.05). Embryo diameter class at recovery did not significantly influence the survival rate. In terms of the embryos that were judged to be alive after 48 h of IVC, quality grade 1 was observed in 7/8 (88%) and 4/12 (33%) of the SF and VIT embryos, respectively (P < 0.05). After time-lapse analysis, the IVC embryo area as well as growth percentage were statistically higher in the SF than the VIT embryos (P < 0.05). In conclusion, no difference in survival rates was found between the two cryopreservation procedures, although embryo quality was more negatively affected by vitrification.
胚胎冷冻保存可确保遗传生物多样性随时间得以保存。本研究评估了经缓慢冷冻和玻璃化冷冻处理后的驴胚胎在解冻及体外培养后的存活率。将体内产生的7日龄驴胚胎进行缓慢冷冻(SF,n = 14)或玻璃化冷冻(VIT,n = 22)。冷冻保存一年后,将胚胎解冻、清洗并置于培养箱中进行体外培养(IVC)。为评估胚胎活力,在解冻后以及体外培养24小时和48小时后记录胚胎的质量等级和发育阶段。11个胚胎(SF = 4个,VIT = 7个)在延时摄像下培养长达68小时,以确定其面积和生长情况。存活率不受冷冻方法的影响,而是受发育阶段的影响:体外培养48小时后,囊胚的存活率(1/8,12.5%)显著低于桑葚胚(8/12,66.7%)和早期囊胚(11/16,68.7%)(P < 0.05)。复苏时的胚胎直径类别对存活率没有显著影响。就体外培养48小时后被判定存活的胚胎而言,SF组和VIT组胚胎中质量等级为1级的分别占7/8(88%)和4/12(33%)(P < 0.05)。经过延时分析,体外培养胚胎的面积以及生长百分比在SF组中在统计学上高于VIT组胚胎(P < 0.05)。总之,两种冷冻保存方法的存活率没有差异,尽管玻璃化冷冻对胚胎质量的负面影响更大。