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Improvement of the developmental competence of canine oocyte using caffeine supplementation during IVM at different maturation time

机译:不同成熟时间IVM中咖啡因补充剂在IVM期间使用咖啡因补充剂的提高

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摘要

The aim of the current study was to investigate the effect of caffeine supplementation during in vitro maturation (IVM) for different maturation times on the developmental potential of canine oocytes recovered from ovariohysterectomized bitches. The recovered cumulus-oocytes complexes were in vitro matured for 72 h. Here, 10 mM caffeine was added to the maturation medium for different incubation times (caffeine from 0-72 h maturation, caffeine for the first 24 h of maturation only, caffeine addition from 24 to 48 h maturation time, caffeine addition from 48 to 72 h maturation or in caffeine-free medium, control group). The matured oocytes were in vitro fertilized using frozen-thawed spermatozoa. The presumptive zygotes were in vitro cultured in synthetic oviductal fluid medium for 5 days. The results showed that both maturation and fertilization rates were significantly higher (P 0.05) using caffeine-treated medium for the first 24 h of maturation compared with the control and other two groups of caffeine treatment (from 24 to 48 h and from 48 to 72 h), whereas use of caffeine-treated medium for a 0-72 h incubation time did not affect these rates (P 0.05). Interestingly, the matured oocytes in caffeine-supplemented medium for the first 24 h or from 0-72 h showed a significant (P 0.05) increase in the total number of cleaved embryos compared with the control group. In conclusion, supplementation of the maturation medium with 10 mM caffeine for the first 24 h of maturation or during the whole maturation time (0-72 h) improved nuclear maturation and subsequent embryo development preimplantation following in vitro fertilization.
机译:目前研究的目的是探讨咖啡因补充在体外成熟(IVM)期间对不同成熟时间对从卵巢中间母猪中回收的犬卵母细胞的发育潜力的影响。回收的浓度卵母细胞复合物在体外成熟72小时。这里,将10 mm的咖啡因加入到成熟培养基中进行不同孵育时间(咖啡因从0-72小时成熟,咖啡因为前24小时,咖啡因加入24至48 h成熟时间,咖啡因加入48至72 H成熟或无咖啡因培养基,对照组)。使用冷冻过滤的精子,成熟的卵母细胞体外受精。在合成的流体流体介质中培养了推定的Zygotes 5天。结果表明,使用咖啡因处理的培养基与对照和其他两组咖啡因治疗(24至48小时和48组)相比,使用咖啡因处理的培养基(P <0.05)的成熟和施肥率明显高于(P <0.05)。至72小时,而使用咖啡因处理的培养基0-72小时孵育时间不影响这些速率(P& 0.05)。有趣的是,与对照组相比,咖啡因补充培养基中的咖啡因补充培养基中的成熟卵母细胞显示出显着的(P <0.05)增加的裂解胚胎总数。总之,在进行成熟的前24小时或在整个成熟时间(0-72小时)改善核成熟和随后在体外受精后的核成熟和随后的胚胎发育前预约。

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