Bergstein-Galan Tácia Gomes, Weiss Romildo Romualdo, Kozicki Luiz Ernandes, Bicudo Sony Dimas
Department of Technology, Postgraduate studies in Bioprocess Engineering and Biotechnology, Human and Animal Health, Federal University of Paraná, Rua dos Funcionários, 1540, Curitiba, Paraná, Brazil.
Department of Technology, Postgraduate studies in Bioprocess Engineering and Biotechnology, Human and Animal Health, Federal University of Paraná, Rua dos Funcionários, 1540, Curitiba, Paraná, Brazil.
Anim Reprod Sci. 2017 Dec;187:20-27. doi: 10.1016/j.anireprosci.2017.10.001. Epub 2017 Oct 5.
The objectives of this study were threefold: to identify subpopulations of sperm based on the kinetics of frozen/thawed sheep epididymal spermatozoa or semen collected with an artificial vagina; to evaluate the effects on sperm subpopulations in the thawed samples of post mortem storage at room temperature and the addition of 20% of seminal plasma to the freezing extender and to correlate the percentage of subpopulations with gestation rate following artificial intrauterine insemination. The categorization of the subpopulations was based on sperm kinetic data from Computer Assisted Sperm Analysis (CASA). A hundred ewes were inseminated with thawed spermatozoa and gestation rate was correlated with the proportions of each subpopulation using Pearson correlation matrix and linear regression. Three distinct subpopulations were identified in the thawed samples of either ovine ejaculate collected in artificial vaginas (AV) or ovine spermatozoa retrieved from the cauda epididymis. Subpopulation 1 (SP1) was characterized by spermatozoa with slow and non-linear motion, subpopulation 2 (SP2) was classified as hyperactived spermatozoa and subpopulation 3 (SP3) was composed of spermatozoa with fast, linear motion. The largest subpopulation in all groups was SP1. The semen collected in an artificial vagina had a higher (P<0.05) percentage of SP2 and lower (P<0.05) percentage of SP1 when compared to spermatozoa recovered after death. Increasing time of storage after death had a detrimental effect on sperm samples, increasing (P<0.05) the percentage of SP1 and decreasing (P<0.05) SP2. Length of storage after death was the only variable that influenced, with an inversely proportional relationship, SP3. In samples stored for 48h after death no SP3 spermatozoa were present. The addition of seminal plasma to the cryopreservative decreased (P<0.05) the subpopulation of hyperactived spermatozoa (SP2). We conclude that, after thawing there are three sperm subpopulations in the spermatozoa obtained from the cauda epididymides and the semen collected in AVs and that the relative proportions of these subpopulations varies with the time of storage post mortem and the presence of 20% of seminal plasma in the extender. However, we conclude that these subpopulations do not correlate with fertility after intrauterine artificial insemination.
基于冷冻/解冻的绵羊附睾精子或用人工阴道采集的精液的动力学来识别精子亚群;评估室温下死后储存以及在冷冻稀释液中添加20%精浆对解冻后样品中精子亚群的影响,并将亚群百分比与人工子宫内授精后的妊娠率相关联。亚群的分类基于计算机辅助精子分析(CASA)的精子动力学数据。用解冻的精子对100只母羊进行授精,并使用Pearson相关矩阵和线性回归将妊娠率与每个亚群的比例相关联。在用人造阴道采集的绵羊射精样本或从附睾尾部获取的绵羊精子的解冻样本中,鉴定出三个不同的亚群。亚群1(SP1)的特征是精子运动缓慢且非线性,亚群2(SP2)被归类为超活化精子,亚群3(SP3)由运动快速、线性的精子组成。所有组中最大的亚群是SP1。与死后回收的精子相比,用人造阴道采集的精液中SP2的百分比更高(P<0.05),而SP1的百分比更低(P<0.05)。死后储存时间的延长对精子样本有不利影响,SP1的百分比增加(P<0.05),而SP2的百分比降低(P<0.05)。死后储存时间是唯一影响SP3的变量,且呈反比关系。在死后储存48小时的样本中,不存在SP3精子。向冷冻保存剂中添加精浆会降低(P<0.05)超活化精子亚群(SP2)。我们得出结论,解冻后,从附睾尾部获得的精子以及用人造阴道采集的精液中有三个精子亚群,并且这些亚群的相对比例随死后储存时间以及稀释液中20%精浆的存在而变化。然而,我们得出结论,这些亚群与子宫内人工授精后的生育力无关。