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首页> 外文期刊>Animal Reproduction Science >Dialysis of the goat semen and its effect on the quality of frozen/thawed spermatozoa processed in the presence of egg yolk
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Dialysis of the goat semen and its effect on the quality of frozen/thawed spermatozoa processed in the presence of egg yolk

机译:山羊精液的透析及其对在蛋黄存在下加工冷冻/解冻精子的质量的影响

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摘要

The aim of the present study was to analyze the effect of dialysis on the quality of frozen/thawed buck semen. Ejaculates (n = 15) from three Saanen bucks were divided into three experimental groups. Semen in Group Ce (centrifugation) was processed by standard method and washed two times at 1.085 x g for 20 min. During this time, the diluted control semen (Co) was stored at room temperature. Semen in Group D was dialyzed using 300 kDa cut-off semi-permeable cellulose tubing. The semen from all groups was diluted with extender containing 20% egg yolk and frozen in liquid nitrogen vapor. After thawing, semen samples were evaluated by microscopic and biochemical analyses. Phospholipase A2 was in amounts that was 72.0 +/- 11.7% less after dialysis and 21.3 +/- 10.0% less after washing with centrifugation compared to the control semen (P & 0.05). Spermatozoa from Group Co had a lesser motility and viability and greater percentage of morphological abnormal spermatozoa in comparison to Groups D and Ce at 3 h after thawing and incubation on 37 degrees C. At the same time motility and percentage of HOST positive spermatozoa were greater in Group Ce compared with D (P & 0.05). There, however, was no difference in morphology and viability (CFDA/PI analysis) of spermatozoa between Ce and D group. Results from the present study suggest the dialysis is the promising alternative method for reducing phospholipase A2 in the buck semen before cryopreservation.
机译:本研究的目的是分析透析对冷冻/解冻的精液质量的影响。从三个Saanen降压的射精(n = 15)分为三个实验组。通过标准方法处理Ce(离心)的精液,并在1.085×g下洗涤20分钟。在此期间,将稀释的对照精液(CO)储存在室温下。 D组中的精液使用300kDa截止半透纤维素管透析。来自所有基团的精液用含有20%蛋黄的增量剂稀释,并在液氮蒸汽中冷冻。解冻后,通过显微镜和生物化学分析评估精液样品。磷脂酶A2的量为透析后少于72.0 +/- 11.7%,与对照精液相比,在用离心后较少21.3 +/- 10.0%(P& 0.05)。来自组的Spermatozoa具有较小的动力和可行性,并且在3小时内与3小时进行了较小的动态异常精子,并且在37摄氏度下孵育的同一组和培养率为3小时,同时宿主阳性精子的运动和百分比更大组CE与D(P& LT; 0.05)相比。然而,在CE和D组之间的精子的形态和活力(CFDA / PI分析)无差异。本研究的结果表明,透析是在冷冻保存之前减少降压精液中的磷脂酶A2的有前途的替代方法。

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