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玻璃化冷冻猪胚胎的体外复温后活力:冷冻保存时间的影响。

In vitro postwarming viability of vitrified porcine embryos: effect of cryostorage length.

机构信息

Department of Animal Medicine and Surgery, Faculty of Veterinary Medicine, University of Murcia, E-30071 Murcia, Spain.

出版信息

Theriogenology. 2010 Aug;74(3):486-90. doi: 10.1016/j.theriogenology.2010.03.003. Epub 2010 May 8.

DOI:10.1016/j.theriogenology.2010.03.003
PMID:20452005
Abstract

Porcine embryos, which had been vitrified and stored in liquid nitrogen for up to three yr, were retrospectively analyzed to evaluate the influence of duration of storage on their in vitro viability post-warming. All embryos were vitrified (OPS or SOPS) and warmed (three-step or direct warming) using procedures that resulted in the same in vitro survival, hatching rates, and numbers of cells. Therefore, embryo data obtained using the different procedures were pooled according to their developmental stage as morulae (n = 571) or blastocysts (n = 797) and to the length of their storage in liquid nitrogen: a) 1-9 d; b) 10-30 d; c) 31-90 d; d) 1-3 yr. Non-vitrified embryos of corresponding developmental stages were used as a fresh control group (n = 280). Survival and hatching rates were evaluated after in vitro culture to assess embryo viability. The total number of cells was counted in the resulting viable blastocysts as an indicator of quality. A total of 1,648 fresh and vitrified embryos were analyzed. In vitro survival and hatching rates, but not the number of cells, differed significantly between vitrified morulae and their fresh counterparts irrespective of the duration of cryostorage. Length of storage in liquid nitrogen (LN(2)) did not influence in vitro viability among different groups of vitrified/warmed morulae nor embryos at the blastocyst stage. In conclusion, duration of storage in LN(2) has no effect on the post-warming viability of porcine embryos vitrified at morula or blastocyst stage.

摘要

将猪胚胎进行玻璃化冷冻并储存在液氮中长达 3 年,然后对其进行回顾性分析,以评估储存时间对胚胎解冻后体外活力的影响。所有胚胎均采用 OPS 或 SOPS 方法进行玻璃化冷冻,并采用三步法或直接法进行解冻,这两种方法均能达到相同的体外存活率、孵化率和细胞数量。因此,根据不同的处理程序将胚胎数据按照其发育阶段(桑葚胚,n=571;囊胚,n=797)以及在液氮中储存的时间(a)1-9 天;(b)10-30 天;(c)31-90 天;(d)1-3 年进行分组。同时,还将相应发育阶段的非玻璃化冷冻胚胎作为新鲜对照组(n=280)。在体外培养后评估胚胎的存活率和孵化率,以评估胚胎的活力。对形成的可存活囊胚进行总细胞计数,作为质量的指标。共分析了 1648 个新鲜和玻璃化冷冻的胚胎。体外存活率和孵化率,但不是细胞数量,在玻璃化冷冻的桑葚胚与其新鲜对照组之间存在显著差异,而与冷冻储存时间无关。在不同的玻璃化冷冻/解冻桑葚胚组和囊胚组中,液氮储存时间(LN2)对体外活力均无影响。总之,在桑葚胚或囊胚阶段对猪胚胎进行玻璃化冷冻时,储存时间对解冻后的活力没有影响。

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