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Resveratrol enhances the clearance of mitochondrial damage by vitrification and improves the development of vitrified-warmed bovine embryos

机译:白藜芦醇通过玻璃化增强线粒体损伤的清除,并改善玻璃化加温的牛胚胎的发育

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摘要

The present study investigated the vitrification-induced deterioration of mitochondrial functions that may reduce the developmental ability of post-warming bovine embryos. In addition, the effect of supplementation of the culture medium with resveratrol on the mitochondrial functions and post-warming embryonic development was examined. Two days after in vitro fertilization, embryos with 8–12 cells (referred to hereafter as 8-cell embryos) were vitrified and warmed, followed by in vitro incubation for 5 days in a culture medium containing either the vehicle or 0.5 μM resveratrol. Vitrification reduced embryonic development until the blastocyst stage, reduced the ATP content of embryos, and impaired the mitochondrial genome integrity, as determined by real-time polymerase chain reaction. Although the total cell number and mitochondrial DNA copy number (Mt-number) of blastocysts were low in the vitrified embryos, the Mt-number per blastomere was similar among the blastocysts derived from fresh (non-vitrified) and vitrified-warmed embryos. Supplementation of the culture medium with resveratrol enhanced the post-warming embryonic development and reduced the Mt-number and reactive oxygen species level in blastocysts and blastomeres without affecting the ATP content. An increase in the content of cell-free mitochondrial DNA in the spent culture medium was observed following cultivation of embryos with resveratrol. These results suggested that vitrification induces mitochondrial damages and that resveratrol may enhance the development of post-warming embryos and activates the degeneration of damaged mitochondria, as indicated by the increase in the cell-free mitochondrial DNA content in the spent culture medium and the decrease in the Mt-number of blastocysts and blastomeres.
机译:本研究调查了玻璃化引起的线粒体功能退化,这可能会降低变暖后牛胚胎的发育能力。此外,检查了添加白藜芦醇的培养基对线粒体功能和升温后胚胎发育的影响。体外受精后两天,将具有8-12个细胞的胚胎(以下称为8细胞胚胎)玻璃化并加热,然后在含有媒介物或0.5μM白藜芦醇的培养基中进行体外培养5天。通过实时聚合酶链反应确定,玻璃化作用会减少胚胎发育直至胚泡阶段,降低胚胎的ATP含量,并损害线粒体基因组完整性。尽管玻璃化胚中胚泡的总细胞数和线粒体DNA拷贝数(Mt数)较低,但在新鲜(未玻璃化)和玻璃化温育胚的胚泡中,每个卵裂球的Mt数相似。补充白藜芦醇的培养基增强了变暖后胚胎的发育,并降低了胚泡和卵裂球中的Mt数量和活性氧水平,而不会影响ATP含量。用白藜芦醇培养胚胎后,观察到用过的培养基中无细胞线粒体DNA含量增加。这些结果表明玻璃化会诱导线粒体损伤,白藜芦醇可能会增强变暖后胚胎的发育并激活受损线粒体的变性,这可以通过用过的培养基中无细胞线粒体DNA含量的增加和线粒体DNA的减少来表明。胚泡和卵裂球的Mt数。

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