Sumigama Shiho, Meyers Stuart
Department of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis CA, USA.
J Med Primatol. 2012 Aug;41(4):278-83. doi: 10.1111/j.1600-0684.2012.00548.x. Epub 2012 Jul 2.
The rate at which lethal intracellular ice formation occurs during cryopreservation is highly dependent on several variables. The objective of this study was to determine the optimal rate at which rhesus sperm can be cooled.
Experiments were performed using three rates of cooling. Sperm motility was evaluated by computer-assisted semen analysis, and post-thaw viability was determined using propidium iodide labeling and flow cytometry. Semen was frozen at three cooling rates: (i) fast, (ii) slow, and (iii) standard. Straws were thawed for 30 s at 37°C for analysis of motility and viability.
Post-thaw motility and viability were comparable between freezing curves. Sperm cryopreserved using the slow freeze curve exhibited lowest motility and viability.
This study indicates that macaque sperm survive cooling optimally when cooling rates range from -17 to -34°C/minute. Conversely, slow cooling was detrimental and resulted in poor quality sperm.
冷冻保存过程中致死性细胞内冰晶形成的速率高度依赖于几个变量。本研究的目的是确定恒河猴精子的最佳冷却速率。
使用三种冷却速率进行实验。通过计算机辅助精液分析评估精子活力,并使用碘化丙啶标记和流式细胞术测定解冻后活力。精液以三种冷却速率冷冻:(i)快速,(ii)缓慢,和(iii)标准。吸管在37°C解冻30秒以分析活力和生存能力。
冷冻曲线之间解冻后的活力和生存能力相当。使用缓慢冷冻曲线冷冻的精子表现出最低的活力和生存能力。
本研究表明,当冷却速率在-17至-34°C/分钟范围内时,猕猴精子在冷却过程中能最佳存活。相反,缓慢冷却有害,会导致精子质量差。