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首页> 外文期刊>The Journal of Reproduction and Development >Determination of optimal conditions for parthenogenetic activation and subsequent development of rat oocytes in vitro
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Determination of optimal conditions for parthenogenetic activation and subsequent development of rat oocytes in vitro

机译:确定孤雌性激活和大鼠卵母细胞体外发育的最佳条件

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The present study was undertaken to determine optimal conditions for parthenogenetic activation and subsequent development of rat oocytes. Oocytes from immature Wistar-Imamichi (WI) and Sprague Dawley (SD) rats were activated by electrical stimulation in combination with 6-dimethylaminopurine (6-DMAP) to assess whether different rat strains display different responses to activation treatment. Since the cleavage rates of activated oocytes were significantly higher in WI than SD strain rats, WI rats were used for the subsequent experiments to determine the effects of post-hCG time, culture duration, different activation protocols (electrical stimulation with 6-DMAP or ionomycin with 6-DMAP) and osmolarity of the activation medium on the activation and subsequent development of WI rat oocytes. For oocytes activated by electrical stimulation combined with 6-DMAP, the percentages of oocytes that were activated and that developed to blastocysts were higher when oocytes were collected at 18-20 h than at any other time points after hCG injection (16, 22-24 h). Culturing for 2-6 h before activation treatment markedly decreased the percentage of activated oocytes that developed to beyond the four-cell stage. There were no differences in the percentages of oocytes with pronuclear formation and subsequent development to the two-cell and blastocyst stages between oocytes that were activated by electrical stimulation or ionomycin, both followed by 6-DMAP treatment. Activation of oocytes by ionomycin and 6-DMAP, both in low osmolarity media (246 mOsM), markedly increased the cleavage rates and percentages of high quality blastocysts (71%). The optimal conditions determined in the present study with simplified activation protocols and high efficiency of activation and subsequent development of WI rat oocytes will be helpful for further research involving nuclear transfer in the rat.
机译:进行本研究以确定单性生殖活化和大鼠卵母细胞随后发育的最佳条件。通过电刺激与6-二甲基氨基嘌呤(6-DMAP)结合激活未成熟的Wistar-Imamichi(WI)和Sprague Dawley(SD)大鼠的卵母细胞,以评估不同的大鼠品系是否对激活处理表现出不同的反应。由于WI中活化卵母细胞的裂解率显着高于SD品系大鼠,因此将WI大鼠用于随后的实验以确定hCG后时间,培养时间,不同激活方案(6-DMAP或离子霉素电刺激)的影响(6-DMAP)和渗透压对WI大鼠卵母细胞的激活和后续发育的影响。对于通过电刺激结合6-DMAP激活的卵母细胞,在hCG注射后18-20 h收集卵母细胞时,被激活并发育为胚泡的卵母细胞百分比更高(16,22-24 H)。在活化处理之前培养2-6小时,显着降低了发育到四细胞阶段以外的活化卵母细胞的百分比。在通过电刺激或离子霉素激活并随后进行6-DMAP处理的卵母细胞之间,具有前核形成的卵母细胞百分比以及随后发育为两细胞和胚泡阶段的卵母细胞百分比没有差异。在低渗透压介质(246 mOsM)中,离子霉素和6-DMAP激活卵母细胞均显着提高了卵裂率和高质量囊胚的百分比(71%)。在本研究中确定的最佳条件,具有简化的激活方案,较高的激活效率和WI大鼠卵母细胞的后续发育,将有助于涉及大鼠核转移的进一步研究。

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