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Recovery of mitochondrial function and endogenous antioxidant systems in vitrified bovine oocytes during extended in vitro culture.

机译:在延长的体外培养过程中,玻璃化牛卵母细胞中线粒体功能和内源性抗氧化系统的恢复。

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This study was designed to examine the recovery of mitochondrial function and endogenous antioxidant systems in vitrified oocytes during extended incubations. After 16 hr of in vitro maturation, bovine meiosis-II oocytes were vitrified, and then surviving oocytes were cultured an additional 8 hr. ATP content, ATP synthase activity, expression of ATP synthase F0 subunit 6 (ATP6) and 8 (ATP8) genes, and reactive oxygen species (ROS) levels were investigated in the vitrified oocytes during this additional period (4 or 8 hr). The results showed that: (1) the ATP content and ATP synthase activities in vitrified oocytes at 8 hr post-warming (754.6 fmol, 25.9 nmol NADH/min/mg) were significantly higher than in oocytes immediately warmed (568.3 fmol, 8.7 nmol NADH/min/mg), but still lower than in control oocytes (901.5 fmol, 30.7 nmol NADH/min/mg); (2) the relative expression of ATP6 and ATP8 was initially down-regulated in oocytes when they were first warmed, increased by 4 hr post-warming, and were again down-regulated by 8 hr post-warming; (3) ROS levels in oocytes at 0, 4, and 8 hr post-warming were significantly higher than in control oocytes; and (4) after parthenogenetic activation, the blastocyst rate of oocytes at 8 hr post-warming (26.7%) was significantly higher than that of oocytes immediately warmed (16.9%). These results indicated that mitochondrial function and endogenous antioxidant systems recovered significantly better in vitrified-thawed bovine oocytes with 8 hr of additional incubation, but they did not achieve the activity levels found in fresh oocytes.
机译:这项研究旨在检查长期孵育过程中玻璃化卵母细胞中线粒体功能和内源性抗氧化剂系统的恢复情况。体外成熟16小时后,将牛减数分裂II卵母细胞玻璃化,然后将存活的卵母细胞再培养8个小时。研究了ATP含量,ATP合酶活性,ATP合酶F0亚基6( ATP6 )和8( ATP8 )基因的表达以及活性氧(ROS)水平。在这个额外的时间(4或8小时)内,玻璃化的卵母细胞。结果表明:(1)加热后8小时玻璃化卵母细胞中的ATP含量和ATP合酶活性(754.6 fmol,25.9 nmol NADH / min / mg)显着高于立即加热的卵母细胞(568.3 fmol,8.7 nmol) NADH / min / mg),但仍低于对照卵母细胞(901.5 fmol,30.7 nmol NADH / min / mg); (2)最初加热时,卵母细胞中 ATP6 和 ATP8 的相对表达被下调,变暖后4小时增加,然后再次降低-升温后8小时进行调节; (3)加温后0、4和8小时,卵母细胞的ROS水平明显高于对照卵母细胞; (4)孤雌生殖激活后,卵母细胞在升温后8小时的囊胚发生率(26.7%)显着高于立即升温的卵母细胞(16.9%)。这些结果表明,经过8个小时的额外孵育后,在玻璃化解冻的牛卵母细胞中线粒体功能和内源性抗氧化剂系统恢复得更好,但未达到新鲜卵母细胞中的活性水平。

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