Department of Large Animal Diseases with Clinic, Faculty of Veterinary Medicine, Warsaw University of Life Sciences WULS - SGGW, Warsaw, Poland.
Bayern-Genetik GmbH, Kumhausen, Germany.
Reprod Domest Anim. 2020 Jun;55(6):691-700. doi: 10.1111/rda.13666. Epub 2020 Mar 18.
The aim of the present study was to evaluate the effect of sperm selection by single-layer centrifugation (SLC) performed before freezing on sperm quality after thawing of Fleckvieh bull semen. Ejaculates from 22 bulls were collected by artificial vagina and divided into two aliquots. One aliquot (control sample) was diluted with Steridyl and frozen over nitrogen vapour in a Digitcool freezer (IMV Technologies). Sperm from the second aliquot (SLC sample) was selected using the SLC technique with Bovicoll colloid and then frozen over nitrogen vapour in a Digitcool freezer. After thawing, both samples (control and SLC) were evaluated by computer-aided sperm analysis (CASA; SCA 6.4 System; Microptic S.L) for sperm motility parameters. Integrity of the plasma membrane (viability), high mitochondrial membrane potential (HMMP) and acrosome integrity were assessed using a Guava® easyCyte flow cytometer (IMV Technologies). Morphological examination of spermatozoa was performed by Differential Interference Contrast microscopy (Leica DMi8). Morphological examination of live, immobilized spermatozoa was analysed under high magnification (≥6,600×). After thawing, the mean sperm viability of the control sample was 51.57%, compared to 40.37% for the SLC sample (p < .01). HMMP was higher (p < .01) in the control sample (40.37% versus 28.96%), and the mean of live spermatozoa with damaged acrosome was significantly higher (p < .03) in the SLC sample (1.63% versus 1.95%). The mean percentage of motile spermatozoa was 80.17% in the control sample, compared to 75.14% in the SLC sample (p < .0195), and rapid subpopulation reduced from 20.08% to 8.99% (p < .0001) after SLC. Percentage of hyperactivated sperm decreased from 12.23% to 4.28% (p < .0001) after SLC. Given the overall results, the sperm quality of thawed Fleckvieh bull semen was not improved when sperm were selected by SLC before freezing.
本研究的目的是评估在液氮蒸气中冷冻前进行单层离心(SLC)精子选择对弗利克牛精液解冻后精子质量的影响。通过人工阴道收集 22 头公牛的精液,并将其分为两份。一份(对照样品)用 Steridyl 稀释,然后在 Digitcool 冷冻机(IMV Technologies)中液氮蒸气中冷冻。第二份(SLC 样品)用 Bovicoll 胶体进行 SLC 技术选择,然后在 Digitcool 冷冻机中液氮蒸气中冷冻。解冻后,通过计算机辅助精子分析(CASA;SCA 6.4 系统;Microptic S.L)评估两个样品(对照和 SLC)的精子运动参数。使用 Guava®easyCyte 流式细胞仪(IMV Technologies)评估精子质膜完整性(活力)、高线粒体膜电位(HMMP)和顶体完整性。使用相差干涉对比度显微镜(Leica DMi8)对精子形态进行检查。在高倍镜(≥6,600×)下分析活精子和固定精子的形态。解冻后,对照样品的平均精子活力为 51.57%,而 SLC 样品为 40.37%(p<.01)。对照样品的 HMMP 更高(p<.01)(40.37%对 28.96%),并且 SLC 样品中顶体受损的活精子平均比例明显更高(p<.03)(1.63%对 1.95%)。对照样品中运动精子的平均百分比为 80.17%,而 SLC 样品为 75.14%(p<.0195),SLC 后快速亚群从 20.08%减少到 8.99%(p<.0001)。超激活精子的百分比从 12.23%减少到 4.28%(p<.0001)。考虑到整体结果,在液氮蒸气中冷冻前通过 SLC 对弗利克牛精液进行精子选择并没有改善解冻后的精子质量。