Department of Veterinary Clinical Sciences, University of Teramo, Viale Crispi 212, 64100 Teramo, Italy.
Theriogenology. 2010 Aug;74(3):424-35. doi: 10.1016/j.theriogenology.2010.02.025. Epub 2010 May 8.
Computer-assisted sperm analyzers (CASA) have become the standard tool for evaluating sperm motility and kinetic patterns because they provide objective data for thousands of sperm tracks. However, these devices are not ready-to-use and standardization of analytical practices is a fundamental requirement. In this study, we evaluated the effects of some settings, such as frame rate and frames per field, chamber and time of analysis, and samples preparations, including thawing temperature, sperm sample concentration, and media used for dilution, on the kinetic results of bovine frozen-thawed semen using a CASA. In Experiment 1, the frame rate (30-60 frame/s) significantly affected motility parameters, whereas the number of frames per field (30 or 45) did not seem to affect sperm kinetics. In Experiment 2, the thawing protocol affects sperm motility and kinetic parameters. Sperm sample concentration significantly limited the opportunity to perform the analysis and the kinetic results. A concentration of 100 and 50 x 10(6) sperm/mL limited the device's ability to perform the analysis or gave wrong results, whereas 5, 10, 20, and 30 x 10(6) sperm/mL concentrations allowed the analysis to be performed, but with different results (Experiment 3). The medium used for the dilution of the sample, which is fundamental for a correct sperm head detection, affects sperm motility results (Experiment 4). In this study, Makler and Leja chambers were used to perform the semen analysis with CASA devices. The chamber used significantly affected motility results (Experiment 5). The time between chamber loading and analysis affected sperm velocities, regardless of chamber used. Based on results recorded in this study, we propose that the CASA evaluation of motility of bovine frozen-thawed semen using Hamilton-Thorne IVOS 12.3 should be performed using a frame rate of 60 frame/s and 30 frames per field. Semen should be diluted at least at 20 x 10(6) sperm/mL using PBS. Furthermore, it is necessary to consider the type of chamber used and perform the analysis within 1 or 2 min, regardless of the chamber used.
计算机辅助精子分析(CASA)已成为评估精子活力和运动模式的标准工具,因为它为数千个精子轨迹提供了客观数据。然而,这些设备并非即插即用,分析实践的标准化是一个基本要求。在这项研究中,我们评估了一些设置,例如帧率和每视场帧数、室温和分析时间以及样本制备,包括解冻温度、精子样本浓度和用于稀释的介质,对使用 CASA 评估牛冷冻-解冻精液的动力学结果的影响。在实验 1 中,帧率(30-60 帧/秒)显著影响运动参数,而每视场帧数(30 或 45)似乎不影响精子动力学。在实验 2 中,解冻方案会影响精子活力和动力学参数。精子样本浓度显著限制了分析的机会和动力学结果。浓度为 100 和 50×106 精子/ml 限制了设备进行分析的能力或给出错误的结果,而浓度为 5、10、20 和 30×106 精子/ml 浓度允许进行分析,但结果不同(实验 3)。用于稀释样本的介质,对于正确检测精子头至关重要,会影响精子活力结果(实验 4)。在这项研究中,使用 Makler 和 Leja 室与 CASA 设备一起进行精液分析。使用的室对活力结果有显著影响(实验 5)。室加载和分析之间的时间间隔会影响精子速度,而与使用的室无关。基于本研究记录的结果,我们建议使用 Hamilton-Thorne IVOS 12.3 对牛冷冻-解冻精液的 CASA 评估,使用 60 帧/秒的帧率和 30 帧/视场。精液应至少稀释至 20×106 精子/ml 使用 PBS。此外,无论使用哪种室,都有必要考虑使用的室类型,并在 1 或 2 分钟内进行分析。