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The nuclear DNA longevity in cryopreserved boar spermatozoa assessed using the Sperm-Sus-Halomax

机译:使用Sperm-Sus-Halomax评估低温保存的公猪精子的核DNA寿命

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The aim of this experimental study was to evaluate the dynamics of nuclear DNA fragmentation in frozen-thawed (FT) boar spermatozoa incubated over time. Using the Sperm Chromatin Dispersion test (Sperm-Sus-Halomax), this study focused special attention on resolving the hypothesis that the original halo shapes around the sperm head could show dynamic changes over the postthawing incubation time. Twenty FT sperm samples from five boars (four per boar) were incubated at 37 degrees C during 168 hours and sperm motility (assessed using computer-assisted sperm analysis), viability (evaluated using the LIVE/DEAD Sperm Viability Kit), and nuclear DNA fragmentation were analyzed at 0, 0.5, 2, 4, 6, 24, 48, 72, and 168 hours. The percentages of motile and viable spermatozoa progressively decreased during incubation, with no motile and viable spermatozoa less than 10% in all boars at 24 hours of incubation. Four different halo shapes around the sperm head were considered in the Sperm Chromatin Dispersion test: normal, small, large scattered (typical fragmented nuclear DNA), and absent halo, all of them coexisting at the same time in the boar FT semen samples. Sperm with a large scattered halo did not change during postthaw, consistently showing percentages less than 5% over time in all boars. In contrast, the other three sperm populations showed a dynamic evolution over incubation time, characterized by a gradual. reduction of sperm with normal halo, proportional to the increment in the sperm showing a small halo, followed by a switch between the sperm with a small halo and sperm with no halo. These results suggest that three of these four sperm populations, those showing small, large scattered, and absent halo, represent spermatozoa with different degrees of nuclear DNA damage, which should be taken into consideration to indicate the percentage of sperm with fragmented nuclear DNA in boar FT semen samples. (C) 2013 Elsevier Inc. All rights reserved.
机译:这项实验研究的目的是评估随着时间的流逝,冻融(FT)公猪精子中核DNA片段的动力学。使用精子染色质分散测试(Sperm-Sus-Halomax),这项研究特别关注解决以下假设:精子头部周围的原始光环形状可能在融化后的孵育时间内显示出动态变化。将来自五个公猪的20个FT精子样品(每个公猪四个)在168小时内于37摄氏度下孵育,并进行精子运动(使用计算机辅助精子分析评估),生存力(使用LIVE / DEAD精子生存力试剂盒评估)和核DNA在0、0.5、2、4、6、24、48、72和168小时分析碎片。在孵化过程中,活动精子和活精子的百分比逐渐降低,在孵育24小时后,所有公猪的活动精子和活精子均不低于10%。在精子染色质分散试验中,精子头部周围有四种不同的光环形状:正常,小,大的分散(典型的核DNA片段化)和无光环,所有这些都同时存在于公猪FT精液样本中。解冻后精子散乱的光环没有变化,所有公猪的精子百分比始终低于5%。相比之下,其他三个精子群体在潜伏时间内表现出动态演变,其特征是渐进的。正常光环的精子减少,与显示小光环的精子的增加成比例,然后在光晕小的精子和无光晕的精子之间切换。这些结果表明,这四个精子种群中的三个,表现出小的,大的散布和不存在的光环,代表了具有不同程度的核DNA损伤的精子,应将其考虑为表明公猪中具有破碎的核DNA的精子的百分比FT精液样品。 (C)2013 Elsevier Inc.保留所有权利。

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