Makarevich Alexander V, Kubovičová Elena, Hegedušová Zdena, Pivko Juraj, Louda František
Institute for Cattle Breeding Ltd Rapotin, Vyzkumniku 267, 788 13 Vikyrovice, Czech Republic.
Zygote. 2012 May;20(2):97-102. doi: 10.1017/S0967199410000675. Epub 2011 Feb 8.
The goal of this study was to examine the effect of insulin-like growth factor I (IGF-I; added during post-thaw culture (48 h)) on the preimplantation viability and quality of cryopreserved bovine in vivo recovered embryos. The morula stage embryos, non-surgically recovered from superovulated dairy cows of Czech Fleckvieh cattle breed, had previously been cryopreserved by a slow freezing technique and stored in liquid nitrogen since 1989-1990. Following thawing, the embryos were cultured for 48 h either alone (no IGF-I) or in the presence of IGF-I (10 or 100 ng/ml); non-cultured embryos served as a control. Thereafter, the embryos were analyzed for cleavage to the blastocyst stage, apoptosis (TUNEL), embryo cell number and quality of actin cytoskeleton. Following post-thaw culture 41% of embryos developed to advanced blastocysts. IGF-I increased this per cent and, at a higher dose, essentially reduced the per cent of degenerated embryos. In cultured embryos, IGF-I at both doses elevated the cell number compared with non-cultured embryos. However, in comparison with embryos cultured without IGF-I, only the higher IGF-I dose resulted in elevating the embryo cell number. The TUNEL index was significantly lowered by IGF-I treatment. Thawed embryos were mostly of the grade III actin type and fewer (12%) had grade II actin, whilst no grade I actin embryos were noted. The addition of IGF-I resulted in the appearance of grade I actin embryos (8.33 and 6.9% for 10 and 100 ng/ml, respectively). These observations indicate that the addition of IGF-I during post-thaw culture can improve the quality of bovine cryopreserved embryos.
本研究的目的是检测胰岛素样生长因子I(IGF-I;在解冻后培养期间(48小时)添加)对体内回收的冷冻保存牛胚胎植入前活力和质量的影响。桑葚胚阶段的胚胎通过非手术方法从捷克弗莱维赫奶牛品种的超排奶牛中回收,此前已通过慢速冷冻技术进行冷冻保存,并自1989 - 1990年以来一直保存在液氮中。解冻后,胚胎单独培养(不添加IGF-I)或在IGF-I(10或100 ng/ml)存在的情况下培养48小时;未培养的胚胎作为对照。此后,分析胚胎发育至囊胚阶段的分裂情况、细胞凋亡(TUNEL法)、胚胎细胞数量和肌动蛋白细胞骨架质量。解冻后培养后,41%的胚胎发育至高级囊胚。IGF-I提高了这一比例,且在较高剂量下,显著降低了退化胚胎的比例。在培养的胚胎中,与未培养的胚胎相比,两种剂量的IGF-I均增加了细胞数量。然而,与未添加IGF-I培养的胚胎相比,只有较高剂量的IGF-I导致胚胎细胞数量增加。IGF-I处理显著降低了TUNEL指数。解冻后的胚胎大多为III级肌动蛋白类型,较少(12%)为II级肌动蛋白,未观察到I级肌动蛋白胚胎。添加IGF-I后出现了I级肌动蛋白胚胎(10和100 ng/ml时分别为8.33%和6.9%)。这些观察结果表明,解冻后培养期间添加IGF-I可以提高冷冻保存牛胚胎的质量。