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首页> 外文期刊>Veterinary Research Forum >Reactive oxygen species level, mitochondrial transcription factor A gene expression and succinate dehydrogenase activity in metaphase II oocytes derived from in vitro cultured vitrified mouse ovaries
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Reactive oxygen species level, mitochondrial transcription factor A gene expression and succinate dehydrogenase activity in metaphase II oocytes derived from in vitro cultured vitrified mouse ovaries

机译:体外培养的玻璃化小鼠卵巢来源的中期II卵母细胞中的活性氧水平,线粒体转录因子A基因表达和琥珀酸脱氢酶活性

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The aim of this study was to evaluate the effects of ovarian tissue vitrification and two-step in vitro culture on the metaphase II (MII) oocyte reactive oxygen species (ROS) level, mitochondrial transcription factor A ( TFAM) expression and succinate dehydrogenase (SDH) activity. After collection of neonatal mouse ovaries, 45 ovaries were vitrified and the others (n = 45) were considered as control. All ovaries were cultured for seven days, and their isolated preantral follicles were cultured in three-dimensional culture system. After 12 days, the follicular development and oocyte maturation were evaluated and compared in vitrified and non-vitrified ovaries. The collected MII oocytes were inseminated with capacitated spermatozoa. Then, the fertilization, embryonic development, ROS level, TFAM gene expression and SDH activity of oocytes were assessed and compared. There was no significant difference between morphology and percentage of normal follicles between vitrified and non-vitrified ovaries at the beginning of culture. The follicular development and hormone level in the vitrified group was significantly lower than non-vitrified group and the ROS concentration in the vitrified group was significantly higher than non-vitrified group after one-week culture. After follicular culture, there was no significant difference in follicular development, oocyte maturation, fertilization rate, TFAM gene expression, ROS level and mitochondrial SDH activity between the groups. This study showed that ovarian tissue vitrification influences the follicular development through increase in ROS level during culture but these harmful effects may be recovered during the follicular culture period. Thus, vitrification and ovarian culture method should be improved.
机译:这项研究的目的是评估卵巢组织玻璃化和两步体外培养对中期II(MII)卵母细胞活性氧(ROS)水平,线粒体转录因子A(TFAM)表达和琥珀酸脱氢酶(SDH)的影响)活动。收集新生小鼠卵巢后,将45个卵巢玻璃化,将其他卵巢(n = 45)作为对照组。将所有卵巢培养7天,并在三维培养系统中培养其分离的窦前卵泡。 12天后,评估和比较玻璃化和非玻璃化卵巢中的卵泡发育和卵母细胞成熟。收集的MII卵母细胞用获能的精子进行授精。然后,评估和比较卵母细胞的受精,胚胎发育,ROS水平,TFAM基因表达和SDH活性。在开始培养时,玻璃化和非玻璃化卵巢之间的形态和正常卵泡的百分比之间没有显着差异。培养1周后,玻璃化组的卵泡发育和激素水平显着低于非玻璃化组,并且玻璃化组的ROS浓度明显高于非玻璃化组。卵泡培养后,两组之间卵泡发育,卵母细胞成熟,受精率,TFAM基因表达,ROS水平和线粒体SDH活性无显着差异。这项研究表明,卵巢组织玻璃化通过培养过程中ROS水平的增加影响卵泡的发育,但这些有害作用可能在卵泡培养期间得以恢复。因此,应该改进玻璃化和卵巢培养方法。

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