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首页> 外文期刊>The Journal of Reproduction and Development >Validation of the sperm quality analyzer and the hypoosmotic swelling test for frozen-thawed ram and minke whale (Balaenoptera bonarensis) spermatozoa
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Validation of the sperm quality analyzer and the hypoosmotic swelling test for frozen-thawed ram and minke whale (Balaenoptera bonarensis) spermatozoa

机译:冷冻解冻的公羊和小须鲸(Balaenoptera bonarensis)精子的精子质量分析仪的验证和低渗溶胀试验

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The object of the present study was to investigate the validation of the sperm quality analyzer (SQA) and the hypo-osmotic swelling (HOS) test with standard sperm analysis methods in frozen-thawed ram and minke whale spermatozoa. In rams, highly significant correlations were observed in the percentage of motile spermatozoa (P<0.01) and sperm concentration (P<0.01) between the standard and SQA methods. But, the percentage of morphologically normal spermatozoa did not significantly correlate between the standard and SQA methods. The percentages of swollen spermatozoa at 15 minutes by the HOS test were significantly correlated with the motility by the standard (P<0.05) and by the SQA (P<0.05) methods. For minke whale spermatozoa, the SVI (sperm viability index) values by the standard method were significantly (P<0.001) correlated with the sperm motility index (SMI) values by SQA. The percentage of motile spermatozoa was also significantly correlated (P<0.01) with the motility measured by SQA. Using different hypo-osmotic solutions and incubation times, the HOS test with 25, 100 and 150 mOsM did not show significant variations. Motility observed by the standard method and the percentage of swollen spermatozoa were significantly correlated (P<0.05). These results indicate that the SQA and HOS test can be utilized to assess the post-thawing motility of ram and minke whale spermatozoa, and that the SQA and HOS test values are significantly correlated in ram spermatozoa. However, sperm concentration and morphologically normal spermatozoa are not assessed accurately by SQA in minke whales.
机译:本研究的目的是研究在冷冻融化的公羊和小鲸鲸精子中使用标准精子分析方法对精子质量分析仪(SQA)的验证和低渗溶胀(HOS)测试。在公羊中,标准方法和SQA方法之间的活动精子百分比(P <0.01)和精子浓度(P <0.01)高度相关。但是,标准和SQA方法之间形态正常的精子百分比没有显着相关。通过HOS试验,在15分钟时精子肿胀的百分比与运动性显着相关(P <0.05)和SQA(P <0.05)。对于小须鲸的精子,标准方法的SVI(精子活力指数)值与SQA的精子活力指数(SMI)值显着相关(P <0.001)。运动精子的百分比也与通过SQA测量的运动性显着相关(P <0.01)。使用不同的低渗透溶液和孵育时间,在25、100和150 mOsM的HOS测试中未显示出显着差异。用标准方法观察到的运动性与精子肿胀的百分比显着相关(P <0.05)。这些结果表明,SQA和HOS测试可用于评估公羊和小须鲸的精子解冻后的运动能力,并且SQA和HOS测试值与公羊的精子显着相关。然而,SQA无法准确评估小须鲸中的精子浓度和形态正常的精子。

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