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Effects of varying the holding temperature and interval from collection to freezing on post-thaw development of bovine embryos in vitro

机译:改变保存温度和从保存到冷冻的间隔时间对牛胚胎解冻后体外发育的影响

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The objective of this study was to evaluate the in vitro development of frozen-thawed bovine embryos held at room temperature or refrigerated for 2, 6 or 12 h prior to freezing. After recovery, embryos were randomly assigned to be placed in holding media for 2 h (n = 131), 6 h (n = 136) or 12 h (n = 133) prior to freezing. Approximately one-half of the embryos were refrigerated (5 degreesC; n = 203) while the remaining half were held at room temperature (22 degreesC; n = 197) until freezing. Embryos were frozen in 10% ethylene glycol and stored in liquid nitrogen. After thawing, embryos were cultured for 72 h in Ham's F-10 media supplemented with 4% fetal bovine serum. Embryos were evaluated for quality and stage of development prior to freezing and after culture. At the end of culture, it was determined if each embryo had developed beyond the stage recorded prior to freezing and if the embryo had hatched from the zona pellucida. The percentage of embryos that developed during culture was greater (P < 0.001) for Grade 1 (81%) than for either Grade 2 (65%) or Grade 3 (48%) embryos. Likewise, a greater proportion (P < 0.001) of Grade I embryos developed to hatched blastocysts (60%) than either Grade 2 (40%) or Grade 3 (24%) embryos. The holding temperature from collection to freezing did not influence embryo development, regardless of the interval from embryo collection to freezing. The proportion of embryos that developed to expanded blastocysts and hatched was greater (P < 0.005) for embryos held 2 h prior to freezing (64%) than for embryos held for 12 h (33%). Hatching rate of embryos held 6 h prior to freezing (54%) tended (P < 0.08) to be lower than the hatching percentage for embryos held for 2 h. Thus, post-thaw embryonic development was impaired the longer embryos were held prior to freezing and temperature during the interval from collection to freezing did not affect post-thaw development
机译:这项研究的目的是评估在室温下保存或在冷冻前冷藏2、6或12 h的冻融牛胚胎的体外发育。恢复后,将胚胎随机分配在保存介质中放置2 h(n = 131),6 h(n = 136)或12 h(n = 133),然后冷冻。将大约一半的胚胎冷冻(5摄氏度; n = 203),而将其余一半保持在室温(22摄氏度; n = 197)下直至冷冻。将胚胎在10%乙二醇中冷冻,并保存在液氮中。解冻后,将胚胎在补充有4%胎牛血清的Ham's F-10培养基中培养72小时。在冷冻之前和培养之后,评估胚胎的质量和发育阶段。在培养结束时,确定每个胚胎是否已经发展到超过冷冻之前记录的阶段,以及该胚胎是否从透明带孵化。 1级(81%)的培养过程中发育的胚胎百分比(P <0.001)大于2级(65%)或3级(48%)的胚胎。同样,比2级(40%)或3级(24%)胚胎发育成孵化胚泡的比例更高(P <0.001)(60%)。无论从胚胎收集到冷冻的间隔时间如何,从收集到冷冻的保持温度都不会影响胚胎的发育。冷冻前2 h的胚胎发育成可膨胀的胚泡并孵出的胚胎比例(P <0.005)大于12 h的胚胎(33%)(P <0.005)。冷冻前6 h保持的胚胎的孵化率(54%)倾向于(P <0.08)低于2 h保持的胚胎的孵化率。因此,解冻后的胚胎发育会受到损害,因为它们在冷冻之前保存的时间更长,并且从收集到冷冻的时间间隔内的温度不会影响解冻后的发育

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