玻璃化液诱导高渗休克后小家鼠卵母细胞的体外成熟。

IF 1.9
Erica Koaski, Cláudia Schneider Colle, Rafael Alonso Salvador, Vera Lucia Lângaro Amaral, Alfred Paul Senn, David Til
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引用次数: 0

摘要

目的:评价玻璃化液诱导高渗休克后胚胎培养基中卵母细胞的体外成熟率。方法:对20只青春期前雌性小鼠进行双侧卵巢切除术。卵巢解剖获得未成熟(Prophase I)卵母细胞(N = 400),分为4组,转移至含有受精培养基(Sydney IVF fertilmedium, Cook®Medical)的培养皿中。对照组(CG)不处理,试验组(G1、G2、G3)用玻璃化液-2 (VI-2: 14 M蔗糖+乙二醇和二甲亚砜)处理30秒,随后:G1:用玻璃化液-2 (DV-2: 0.5M蔗糖)处理30秒;G2: 60秒DV-2;G3: 60秒DV-1(1M蔗糖),180秒DV-2。各组在37℃、5% CO2的培养箱中培养24小时(Thermo模型3110)。在这段时间之后,我们检查了它们的成熟状态。结果:暴露于VI-2、DV-1和DV-2 (G3)的卵母细胞恢复减数分裂并达到MII期的能力最高;但差异无统计学意义(G3 = 50.5% - 49/97;CG = 27.8% - 10/30)。结论:卵母细胞暴露在玻璃化溶液中,以引起渗透性休克,不干扰小鼠卵母细胞减数分裂的恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions.

In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions.

In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions.

Objective: To evaluate in vitro oocyte maturation rates in embryonic culture medium after induction by hyperosmotic shock caused by exposure to vitrification solutions.

Methods: Bilateral oophorectomy was performed on 20 prepubescent female mice (Swiss). Immature (Prophase I) oocytes (N = 400) were obtained by ovarian dissection, divided into 4 groups, and transferred to culture dishes containing fertilization medium (Sydney IVF Fertilization Medium, Cook® Medical). The control group (CG) did not receive treatment, the test groups (G1, G2, G3) were treated with vitrification solution - 2 (VI-2: 14 M sucrose + ethylene glycol and dimethyl sulfoxide) for 30 seconds and subsequently: G1: 30 seconds in devitrification solution - 2 (DV-2: 0.5M sucrose); G2: 60 seconds DV-2; G3: 60 seconds DV-1(1M sucrose) and 180 seconds DV-2. All groups were cultivated for 24 hours in an incubator at 37ºC and 5% CO2 (Thermo model 3110). After this period, we checked their maturation status.

Results: Oocytes exposed to VI-2, DV-1 and DV-2 (G3) showed the highest rate of competence in resuming meiosis and reaching the MII stage; however, there was no statistically significant difference (G3 = 50.5% - 49/97; CG = 27.8% - 10/30).

Conclusions: Oocyte exposure to vitrification solutions, in order to cause osmotic shock, did not interfere with the resumption of meiosis in mice oocytes.

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