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首页> 外文期刊>Journal of reproduction and fertility >Embryo viability, duration of gestation and birth weight in sheep after transfer of in vitro matured and in vitro fertilized zygotes cultured in vitro or in vivo
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Embryo viability, duration of gestation and birth weight in sheep after transfer of in vitro matured and in vitro fertilized zygotes cultured in vitro or in vivo

机译:体外或体内培养的体外成熟和体外受精受精卵转移后绵羊的存活力,妊娠持续时间和出生体重

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摘要

The influence of various in vitro procedures on embryo survival and the production of normal offspring was investigated in sheep. Zygotes produced from in vitro matured (IVM) and fertilized (IVF) oocytes derived from slaughtered Merino ewes were allocated to three culture treatments for 6.5 days. Two groups were cultured in vitro in the absence or presence of oviduct epithelial cells while the third group was cultured in vivo in the oviducts of synchronized ewes. A fourth group of zygotes obtained from superovulated Merino ewes was also cultured in vivo and served as controls. After culture, IVM–IVF morulae and blastocysts, and control embryos were transferred to final recipient ewes. Pregnancy was diagnosed at day 50 of gestation by ultrasonography and pregnancies were allowed to go to term. The survival to term of IVM–IVF zygotes cultured in vitro was reduced compared with both in vivo cultured IVM–IVF zygotes and control zygotes 25–35% versus 51–60%, respectively, P 0.1). Both the gestation period and birth weight of IVM–IVF lambs were increased when compared with controls, the former significantly in all groups (154.0–154.9 days versus 150.6 days; P < 0.01), while the latter increase was on the borderline of significance (4·5–4·8 kg versus 4.0 kg; 0.01 ≤ P ≤ 0.1, respectively) and dependent on the prolongation of the gestation period. It is concluded that in vitro maturation and fertilization compromise subsequent embryonic and fetal development in sheep irrespective of the subsequent in vivo or in vitro culture treatment. Subjecting IVM–IVF zygotes to in vivo culture for 6.5 days minimizes only some of these effects, thus leading to the aberrant production of some offspring.
机译:在绵羊中研究了各种体外程序对胚胎存活和正常后代产生的影响。从屠宰的美利奴羊母羊的体外成熟(IVM)和受精(IVF)卵母细胞产生的合子被分配到三种培养处理中,共6.5天。两组在不存在或不存在输卵管上皮细胞的情况下进行体外培养,而第三组在同步母羊的输卵管中进行体内培养。从超排的美利奴羊母羊获得的第四组合子也进行了体内培养,并作为对照。培养后,将IVM–IVF桑ula和胚泡以及对照胚胎转移至最终的母羊。在妊娠的第50天,通过超声检查诊断出怀孕,允许怀孕。与体内培养的IVM–IVF受精卵和对照受精卵相比,体外培养的IVM–IVF受精卵的存活率分别降低了25–35%(相对于51–60 %)(P 0.1)。与对照组相比,IVM–IVF羔羊的妊娠期和出生体重均增加,前者在所有组中均显着增加(154.0–154.9天比150.6天; P <0.01),而后者的增加处于显着临界水平( 4·5–4·8公斤vs 4.0公斤;分别为0.01≤P≤0.1),并且取决于妊娠期的延长。结论是,不管随后进行的体内或体外培养处理,体外成熟和受精都会损害绵羊随后的胚胎和胎儿发育。使IVM–IVF受精卵在体内培养6.5天,只能将其中的某些影响降至最低,从而导致某些后代的异常产生。

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