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首页> 外文期刊>Zygote >Effect of culture media on porcine embryos produced by in vitro fertilization or parthenogenetic activation after oocyte maturation with cycloheximide
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Effect of culture media on porcine embryos produced by in vitro fertilization or parthenogenetic activation after oocyte maturation with cycloheximide

机译:培养基对环己酰亚胺卵母细胞成熟后体外受精或孤雌激活产生的猪胚胎的影响

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摘要

This study evaluated the effects of reversible meiotic inhibition and different culture media (PZM3 or NCSU23) on production of porcine embryos by either in vitro fertilization (IVF) or parthenogenetic activation (PA). Oocytes from abattoir-derived ovaries were allocated into two groups for maturation: CHX (5 μg/ml cycloheximide for 10 h) or Control (no CHX). The percentage of metaphase II (MII) oocytes was determined at 36, 40 or 44 h of in vitro maturation. For IVF and PA, denuded oocytes were fertilized with purified sperm for 6 h or activated by electric stimuli. Zygotes were then subdivided into two culture groups: NCSU23 or PZM3.No effect of treatment with CHX and culture mediawas observed on cleavage (D3) and blastocyst (D7) rates in IVF and PA groups. There are no differences of quality or development rates between IVF-derived embryos cultured in NCSU23 or PZM3. However, we observed high quality PA embryos in PZM3 compared with NCSU23. Maturation arrest with CHX decreased the average blastocyst cell number in IVF while it was increased in PA embryos. As older oocytes are more effectively activated, CHX- blocked oocytes reached the mature stage faster than the control group. In conclusion, the CHX treatment for 10 h, followed by oocyte maturation for 40 h, is an efficient protocol to produce high quality parthenote embryos, especially when they are cultured in PZM3. However, this protocol is not satisfactory for IVF embryos production. In this case, a shorter maturation period could provide better embryo quality.
机译:这项研究评估了可逆减数分裂抑制和不同培养基(PZM3或NCSU23)对通过体外受精(IVF)或孤雌生殖激活(PA)产生的猪胚胎的影响。将来自屠宰场卵巢的卵母细胞分为两组进行成熟:CHX(5μg/ ml环己酰亚胺10 h)或对照组(无CHX)。在体外成熟36、40或44 h时确定中期II(MII)卵母细胞的百分比。对于IVF和PA,将裸露的卵母细胞与纯化的精子受精6小时或通过电刺激激活。然后将合子分为两个培养组:NCSU23或PZM3。未观察到用CHX和培养基处理对IVF和PA组的卵裂率(D3)和胚泡率(D7)产生影响。在NCSU23或PZM3中培养的IVF来源的胚胎之间,质量或发育速率没有差异。但是,与NCSU23相比,我们在PZM3中观察到了高质量的PA胚胎。 CHX的成熟停滞降低了IVF中的平均胚泡细胞数,而PA胚胎中则增加了。随着更老的卵母细胞被更有效地激活,CHX阻断的卵母细胞比对照组更快地达到了成熟阶段。总之,CHX处理10 h,然后卵母细胞成熟40 h,是生产高质量单性生殖胚胎的有效方案,尤其是在PZM3中培养时。但是,此协议对于IVF胚胎的生产并不令人满意。在这种情况下,较短的成熟期可以提供更好的胚胎质量。

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