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首页> 外文期刊>Molecular reproduction and development >Embryonic and foetal development of bovine oocytes treated with a combination of butyrolactone I and roscovitine in an enriched medium prior to IVM and IVF.
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Embryonic and foetal development of bovine oocytes treated with a combination of butyrolactone I and roscovitine in an enriched medium prior to IVM and IVF.

机译:在IVM和IVF之前,用丁内酯I和roscovitine组合处理的牛卵母细胞的胚胎和胎儿发育。

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摘要

Cattle oocytes were maintained at germinal vesicles (GV) stage for 24 hr using a combination of two specific and potent inhibitors of M-phase promoting factor (MPF) kinase activity, butyrolactone I (BL-I) and roscovitine (ROS). The media used for inhibition were (a) TCM-199 only and (b) TCM-199 supplemented with serum, hormones and growth factors. The effective doses of inhibitors were 6.25 microM BL-I and 12.5 microM ROS in medium (a) and 50 microM BL-I and 12.5 microM ROS in medium (b). After inhibition, about 90% of the oocytes resumed meiosis and reached the metaphase II (MII) stage during 24 hr of maturation. Following fertilisation the percentage of cleavage (D +2), compacted morula (D +6), blastocysts on D +7 and D +8 and the survival to freezing and thawing of grade 1 embryos frozen on D +7 were not different between the experimental treated groups and the control. In order to evaluate early foetal development, two groups of five grade 1 D +7 blastocysts derived from treated oocytes and two groups of five control embryos were transferred nonsurgically in four synchronised recipient heifers. On D +27, the recipients were slaughtered and the foetuses were recovered. In both groups, six foetuses developed out of the 10 embryos transferred. In conclusion, several supplements can be added to the prematuration medium of bovine oocytes without reducing the quality of inhibition but also without improving their subsequent developmental competence versus treated oocytes in TCM-199 only and versus untreated control. Furthermore, the prematuration step used in this study does not interfere with normal foetal development during the first stages of organogenesis.
机译:牛卵母细胞通过使用M-阶段促进因子(MPF)激酶活性的两种特异性抑制剂,丁内酯I(BL-1)和roscovitine(ROS)的组合在生小泡(GV)阶段保持24小时。用于抑制的培养基是(a)仅TCM-199和(b)补充了血清,激素和生长因子的TCM-199。抑制剂的有效剂量为在培养基中(a)为6.25 microM BL-1和12.5 microM ROS(b),在培养基中为50 microM BL-1和12.5 microM ROS(b)。抑制后,大约90%的卵母细胞在成熟的24小时内恢复了减数分裂并达到了中期II(MII)阶段。受精后卵裂的百分率(D +2),紧实的桑ula骨(D +6),D +7和D +8的胚泡以及在D +7上冷冻的1级胚胎的冷冻和解冻存活率没有差异。实验治疗组和对照组。为了评估胎儿的早期发育,将两组来自经处理的卵母细胞的五个1D +7级囊胚和两组五个对照组的胚胎非手术地转移到四个同步的受精母牛中。在第+27天,将接受者屠宰,并回收胎儿。两组中,在转移的10个胚胎中都有6个胎儿发育。总之,可以将几种补充剂添加到牛卵母细胞的过早成熟培养基中,而不会降低抑制质量,而且与仅在TCM-199中的未处理卵母细胞以及未处理的对照相比,也不会提高其随后的发育能力。此外,本研究中使用的早产步骤在器官发生的最初阶段不会干扰正常的胎儿发育。

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