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The parthenogenetic activation of canine oocytes with Ca-EDTA by various culture periods and concentrations

机译:Ca-EDTA对犬卵母细胞孤雌生殖的激活作用

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摘要

In the present study, canine oocytes were exposed to various concentrations of and durations of exposure to EDTA saturated with Ca(2+) (Ca-EDTA), a cell membrane-impermeable metal ion chelator, to determine if parthenogenetic activation could be induced. When oocytes were cultured for 48 or 72 h in parthenogenetic activation medium (PAM) without Ca-EDTA (control) or PAM supplemented with 1 or 5mM Ca-EDTA, the highest rate of pronuclear formation (PN) was obtained in oocytes cultured in 1mM Ca-EDTA for 48 h (8.0%; P<0.05). There was no pronuclear formation in the control group (PAM without Ca-EDTA). Oocytes treated with 5mM Ca-EDTA for 48 h or 1mM Ca-EDTA for 72 h formed a parthenogenetic pronucleus (3.1 and 4.5, respectively). However, there was no pronuclear formation in oocytes treated with 5mM Ca-EDTA for 72 h. In summary, exposure to Ca-EDTA can induce pronuclear formation in canine oocytes.
机译:在本研究中,犬卵母细胞暴露于各种浓度和暴露持续时间的EDTA饱和的Ca(2+)(Ca-EDTA),一种细胞膜不可渗透的金属离子螯合剂,以确定是否可以诱导孤雌生殖活化。当卵母细胞在不含Ca-EDTA(对照)或补充有1或5mM Ca-EDTA的PAM的孤雌生殖激活培养基(PAM)中培养48或72 h时,在1mM的卵母细胞中获得最高的前核形成率(PN)。 Ca-EDTA 48小时(8.0%; P <0.05)。对照组(不含Ca-EDTA的PAM)没有前核形成。用5mM Ca-EDTA处理48h或1mM Ca-EDTA处理72h的卵母细胞形成孤雌生殖原核(分别为3.1和4.5)。但是,用5mM Ca-EDTA处理72小时后,卵母细胞中没有原核形成。总之,暴露于Ca-EDTA可以诱导犬卵母细胞中的前核形成。

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