首页> 美国卫生研究院文献>PLoS Clinical Trials >Novel Flow Cytometry Analyses of Boar Sperm Viability: Can the Addition of Whole Sperm-Rich Fraction Seminal Plasma to Frozen-Thawed Boar Sperm Affect It?
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Novel Flow Cytometry Analyses of Boar Sperm Viability: Can the Addition of Whole Sperm-Rich Fraction Seminal Plasma to Frozen-Thawed Boar Sperm Affect It?

机译:新颖的流式细胞术分析公猪精子的存活力:冷冻融化的公猪精子中富含全精子的部分精浆能影响它吗?

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摘要

Boar semen cryopreservation remains a challenge due to the extension of cold shock damage. Thus, many alternatives have emerged to improve the quality of frozen-thawed boar sperm. Although the use of seminal plasma arising from boar sperm-rich fraction (SP-SRF) has shown good efficacy; however, the majority of actual sperm evaluation techniques include a single or dual sperm parameter analysis, which overrates the real sperm viability. Within this context, this work was performed to introduce a sperm flow cytometry fourfold stain technique for simultaneous evaluation of plasma and acrosomal membrane integrity and mitochondrial membrane potential. We then used the sperm flow cytometry fourfold stain technique to study the effect of SP-SRF on frozen-thawed boar sperm and further evaluated the effect of this treatment on sperm movement, tyrosine phosphorylation and fertility rate (FR). The sperm fourfold stain technique is accurate (R2 = 0.9356, p > 0.01) for simultaneous evaluation of plasma and acrosomal membrane integrity and mitochondrial membrane potential (IPIAH cells). Centrifugation pre-cryopreservation was not deleterious (p > 0.05) for any analyzed variables. Addition of SP-SRF after cryopreservation was able to improve total and progressive motility (p < 0.05) when boar semen was cryopreserved without SP-SRF; however, it was not able to decrease tyrosine phosphorylation (p > 0.05) or improve IPIAH cells (p > 0.05). FR was not (p > 0.05) statistically increased by the addition of seminal plasma, though females inseminated with frozen-thawed boar semen plus SP-SRF did perform better than those inseminated with sperm lacking seminal plasma. Thus, we conclude that sperm fourfold stain can be used to simultaneously evaluate plasma and acrosomal membrane integrity and mitochondrial membrane potential, and the addition of SP-SRF at thawed boar semen cryopreserved in absence of SP-SRF improve its total and progressive motility.
机译:由于冷休克损害的扩大,公猪精液的冷冻保存仍然是一个挑战。因此,出现了许多替代方案来提高冻融公猪精子的质量。尽管使用公猪精子富集级分(SP-SRF)产生的精浆显示出良好的疗效;但是,大多数实际的精子评估技术包括单或双精子参数分析,这会高估实际精子的生存能力。在这种情况下,进行这项工作是为了引入一种精子流式细胞仪四重染色技术,以同时评估血浆和顶体膜的完整性以及线粒体膜的潜力。然后,我们使用精子流式细胞仪四重染色技术研究SP-SRF对冻融公猪精子的影响,并进一步评估了该处理对精子运动,酪氨酸磷酸化和受精率(FR)的影响。精子四倍染色技术准确(R 2 = 0.9356,p> 0.01)可同时评估血浆和顶体膜的完整性以及线粒体膜电位(IPIAH细胞)。离心冷冻保存对任何分析变量均无害(p> 0.05)。低温保存后添加SP-SRF可以提高公猪精液的低温和不添加SP-SRF时的总运动能力(p <0.05)。然而,它不能减少酪氨酸磷酸化(p> 0.05)或改善IPIAH细胞(p> 0.05)。精液的添加不会使FR统计学上增加(p> 0.05),尽管用冷冻解冻的公猪精液和SP-SRF授精的雌性的表现要好于缺少精浆的精子。因此,我们得出的结论是,可以使用四倍精子染色法同时评估血浆和顶体膜的完整性以及线粒体膜电位,并且在不存在SP-SRF的情况下冷冻保存的解冻的公猪精液中添加SP-SRF可以改善其总体和进行性运动能力。

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