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In vitro fertilization of in vitro matured canine oocytes using frozen-thawed dog semen

机译:冻融狗精液对体外成熟犬类卵母细胞的体外受精

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摘要

Experiments were conducted to evaluate in vitro fertilization (IVF) of in vitro matured (IVM) bitch oocytes using dog spermatozoa frozen in three different extenders. Sperm-rich fraction from eight ejaculates of five dogs was frozen in each one of three egg yolk Tris extenders with additional: (A) 1.4 g citric acid and 0.8 g glucose; (B) 0.7 g citric acid and 3.5 g glucose; or (C) 1.4 g citric acid and 0.8 g fructose (all with 5% glycerol in 100 mL milliQ water). Thawed sperm were co-incubated with IVM bitch oocytes for 6 h. Oocytes were fixed and evaluated under an epifluorescence microscope; penetrated oocytes were defined as those having sperm heads in the perivitelline space or in the oocyte cytoplasm. Higher penetration rates (P < 0.05) were obtained in oocytes cultured with spermatozoa frozen in extenders B and C than those frozen in extender A (33.1, 34.2 and 26.4%, respectively).
机译:进行了实验,以评估使用三种不同补充剂冷冻的狗精子体外成熟(IVM)母犬卵母细胞的体外受精(IVF)。将来自五只狗的八只精液的富精子级分冷冻在三个蛋黄Tris补充剂中的每一个中,并补充:(A)1.4 g柠檬酸和0.8 g葡萄糖; (B)0.7克柠檬酸和3.5克葡萄糖;或(C)1.4克柠檬酸和0.8克果糖(均在100毫升MilliQ水中含5%甘油)。将解冻的精子与IVM母卵母细胞共同孵育6小时。固定卵母细胞并在落射荧光显微镜下评估;渗透的卵母细胞定义为在卵白质间隙或卵母细胞胞质中具有精子头的卵母细胞。与用增量剂A冷冻的精子相比,用增量剂B和C冷冻的精子培养的卵母细胞获得更高的穿透率(P <0.05)(分别为33.1%,34.2%和26.4%)。

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