首页> 外文期刊>The Indian Journal of Animal Sciences >Developmental competence of goat oocytes vitrified at immature and mature stage in comparsion to fresh oocytes after in vitro fertilization using cauda epididymal spermatozoa
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Developmental competence of goat oocytes vitrified at immature and mature stage in comparsion to fresh oocytes after in vitro fertilization using cauda epididymal spermatozoa

机译:使用Cauda附睾精子的体外施肥后,与新鲜卵母细胞的未成熟和成熟阶段的山羊卵母细胞的发育能力

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摘要

The oocytes were cryopreserved at 2 developmental check points, viz. immature and metaphase II stage, and the outcome of in vitro fertilization (IVF) was assessed as compared to fresh oocytes. The oocytes were cryopreserved by solid surface vitrification technique using equilibration media (4% ethylene glycol) followed by vitrification media (0.5 M sucrose + 35% ethylene glycol + 0.5% polyvinyl pyrollidone). The mature oocytes were pre-treated with cytochalasin B for 30 min before vitrification. The vitrified-thawed oocytes of both groups as well fresh oocytes were fertilized with buck epididymal sperm. The results revealed a significantly higher rate of embryonic development in vitrified-thawed immature oocytes as compared to that in vitrified-thawed mature oocytes at all the embryonic stages. The embryonic developmental rate under fresh oocyte group was significantly higher than both vitrified groups. Results indicated that the immature goat oocytes could be a better candidate for long term storage of female germplasm as well as dissemination into distant places.
机译:卵母细胞在2个发育检查点,viz中被冷冻保存。与新鲜卵母细胞相比,评估未成熟和中期II阶段,以及体外施肥的结果(IVF)。通过使用平衡介质(4%乙二醇)的固体表面玻璃化技术进行冷冻保存卵母细胞,然后用玻璃化培养基(0.5M蔗糖+ 35%乙二醇+ 0.5%聚乙烯醇聚乙烯聚氨酯)。在玻璃化之前将成熟的卵母细胞用细胞蛋白酶B预处理30分钟。随着新鲜卵母细胞的两组玻璃化卵母细胞用降压附睾精子受精。结果表明,与所有胚胎阶段的玻璃化型成熟卵母细胞中相比,玻璃化解冻的未成熟卵母细胞中的胚胎发育率明显较高。新鲜卵母细胞组下的胚胎发育率明显高于玻璃化基团。结果表明,未成熟的山羊卵母细胞可能是女性种质长期储存的更好候选者,也可以传播到遥远的地方。

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