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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >L-Carnitine Supplementation During Vitrification of Mouse Oocytes at the Germinal Vesicle Stage improves Preimplantation Development Following Maturation and Fertilization In Vitro
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L-Carnitine Supplementation During Vitrification of Mouse Oocytes at the Germinal Vesicle Stage improves Preimplantation Development Following Maturation and Fertilization In Vitro

机译:小鼠卵母细胞在胚泡阶段玻璃化期间补充左旋肉碱可改善成熟和体外受精后的植入前发育

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摘要

Oocyte cryopreservation is important for assisted reproductive technologies (ART). Although cryopreservation of meta-phase II (MM) oocytes has been successfully used, Mil oocytes are vulnerable to the damage inflicted by the freezing procedure. Cryopreservation of germinal vesicle stage oocytes (GV-oocytes) is an alternative choice; however, blastocyst development from GV-oocytes is limited largely due to the need for in vitro maturation (IVM). Herein, we evaluated the effects of L-carnitine (LC) supplementation during vitrification and thawing of mouse GV-oocytes, IVM, and embryo culture on preimplantation development after in vitro fertilization (IVF). We first compared the rate of embryonic development from the oocytes that had been collected at the GV stage from three mouse strains, (B6.DBA)F1, (B6.C3H)F1, and B6, and processed for IVM and IVF, as well as that from the oocytes matured in vivo, i.e. ovulated (IVO). Our results demonstrated that the rate of blastocyst development was the highest in the (B6.DBA)F1 strain and the lowest in the B6 strain. We then supplemented the IVM medium with 0.6 mg/ml LC. The rate of blastocyst development improved in the B6 but not in the (B6.DBA)F1 strain. Vitrification of GV-oocytes in the basic medium alone reduced the rate of blastocyst development in both of those mouse strains. LC supplementation to the IVM medium alone did not change the percentage of blastocyst development. However, LC supplementation to both vitrification and IVM media significantly improved blastocyst development to the levels comparable with those obtained from vitrified/thawed IVO oocytes in both of the (B6.DBA)F1 and B6 strains. We conclude that LC supplementation during vitrification is particularly efficient in improving the preimplantation development from the GV-oocytes that otherwise have lower developmental competence in culture.
机译:卵母细胞冷冻保存对于辅助生殖技术(ART)很重要。尽管已经成功地使用了II期(MM)卵母细胞的冷冻保存,但Mil卵母细胞容易受到冷冻程序造成的损害。冷冻保存生泡阶段卵母细胞(GV-卵母细胞)是另一种选择。然而,由于需要体外成熟(IVM),因此GV卵母细胞的胚泡发育受到很大限制。在这里,我们评估了在体外受精(IVF)后小鼠GV卵母细胞,IVM和胚胎培养的玻璃化和解冻过程中补充左旋肉碱(LC)对植入前发育的影响。我们首先比较了从GV阶段从三种小鼠品系(B6.DBA)F1,(B6.C3H)F1和B6采集并经IVM和IVF处理的卵母细胞中胚胎发育的速率因为卵母细胞在体内成熟,即排卵(IVO)。我们的结果表明,胚泡发育率在(B6.DBA)F1菌株中最高,而在B6菌株中最低。然后,我们用0.6 mg / ml LC补充了IVM培养基。 B6中胚泡发育的速率提高了,但(B6.DBA)F1株却没有。仅在基本培养基中对GV卵母细胞进行玻璃化会降低这两种小鼠品系中胚泡发育的速度。仅向IVM培养基添加LC并不会改变胚泡发育的百分比。但是,在玻璃化和IVM培养基中添加LC可以显着改善囊胚发育,使其水平与(B6.DBA)F1和B6菌株中从玻璃化/融化的IVO卵母细胞获得的水平相当。我们得出结论,玻璃化过程中的LC补充在改善GV卵母细胞着床前发育方面特别有效,而GV卵母细胞在培养中的发育能力较低。

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