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Changes in subpopulations of boar sperm defined according to viability and plasma and acrosome membrane status observed during storage at 15 degrees C

机译:在15摄氏度下储存期间观察到的根据生存能力以及血浆和顶体膜状态确定的公猪精子亚群的变化

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Four boar ejaculates were preserved for 42d at 15 degrees C to examine the changes produced in the quality of sperm membranes according to their response to a combined short hypoosmotic swelling test (sHOST) plus viability test designated the sHV test. Every 1 or 2d, a sample from each ejaculate preserved in long-term extender was subjected to sperm motility determination and the sHV test. Through simultaneous examination by phase contrast and fluorescence microscopy, three subpopulations of spermwere identified according to their response to sHOST challenge and their viability status. In the subpopulations scoring positive in the sHOST, a further four sperm subpopulations were defined according to their viability and acrosome status. All the sperm subpopulations differed in terms of changes in their proportions produced during the course of preservation and individual differences among ejaculates were detected in terms of relationships shown among subpopulations. The combined sHOST/viability test was able to identify sperm subpopulations with the strongest plasma and acrosome membranes as well as a subpopulation of sperm that had undergone a true acrosome reaction.
机译:将四头公猪射精在15摄氏度下保存42天,以检查它们对组合的短渗透性溶胀试验(sHOST)和活力试验(称为sHV试验)的反应,从而改变精子膜质量。每隔1或2天,对长期保存在延长液中的每个射精样本进行精子活力测定和sHV测试。通过相衬检查和荧光显微镜术同时检查,根据精子对sHOST攻击的反应和生存能力,鉴定出三个亚群。在sHOST中得分为阳性的亚群中,根据其生存力和顶体状态定义了另外四个精子亚群。所有精子亚群在保存过程中产生的比例变化方面都不同,并且根据亚群之间显示的关系检测到射精之间的个体差异。组合的sHOST /生存力测试能够鉴定出具有最强血浆和顶体膜的精子亚群,以及经历了真正顶体反应的精子亚群。

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