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Effects of in vitro growth culture duration and prematuration culture on maturational and developmental competences of bovine oocytes derived from early antral follicles

机译:体外培养时间和早熟培养对早期窦房卵泡卵母细胞成熟和发育能力的影响

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Bovine ovaries offer a large pool of oocytes that could be used for in vitro production of embryos of genetically valuable animals. The effects of in vitro growth (IVG) culture duration (10, 12, and 14 days) on the viability and growth of bovine oocytes derived from early antral follicles (0.5-1 mm diameter) in this study. In addition, the effect of pre-IVM culture with phosphodiesterase inhibitor (3-isobutyl-1-methylxanthine) on nuclear maturation of IVG oocytes was also evaluated. In experiment 1, oocyte viability observed after 10 or 12 days of IVG culture was greater (P < 0.05) than that observed after 14 days of culture. Oocyte diameters and proportions of oocytes at metaphase II stage were greater (P < 0.05) when 12 or 14 days of IVG culture where used when compared with 10 days culture. In addition, the proportion of oocytes at metaphase II stage was greater (P < 0.05) when pre-IVM culture was performed for oocytes derived from 12 and 14 days of IVG culture. When 12 and 14 days of IVG culture followed by pre-IVM culture were compared in experiment 2, cumulus cell membrane integrity was greater (P < 0.05) after 12 days. Blastocyst production rate for oocytes obtained after 12 days of IVG culture (24.5%) was greater (P < 0.05) than for oocytes obtained after 14 days (9.9%). In conclusion, 12 days IVG followed by pre-IVM culture was considered the optimal processing system for bovine oocytes derived from early antral follicles when oocyte viability, diameter, maturation, and development competences were considered
机译:牛卵巢提供大量卵母细胞,可用于体外生产具有遗传价值的动物的胚胎。在这项研究中,体外生长(IVG)培养持续时间(10、12和14天)对源自早期肛门窦卵泡(直径为0.5-1 mm)的牛卵母细胞活力和生长的影响。此外,还评估了用磷酸二酯酶抑制剂(3-异丁基-1-甲基黄嘌呤)进行IVM前培养对IVG卵母细胞核成熟的影响。在实验1中,IVG培养10或12天后观察到的卵母细胞存活力比培养14天后观察到的更大(P <0.05)。当使用IVG培养12或14天时,与10天培养相比,在II期中期的卵母细胞直径和卵母细胞比例更大(P <0.05)。另外,当对IVG培养的12天和14天的卵母细胞进行IVM前培养时,处于中期II期的卵母细胞比例更大(P <0.05)。在实验2中比较了IVG培养和IVM前培养的12天和14天后,卵丘细胞膜完整性在12天后更大(P <0.05)。 IVG培养12天后获得的卵母细胞的胚泡产生率(24.5%)大于14天后获得的卵母细胞的囊胚产生率(9.9%)。总之,在考虑卵母细胞的生存力,直径,成熟度和发育能力后,IVG继之于IVM前培养的12天被认为是源自早期肛门卵泡的牛卵母细胞的最佳加工系统。

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