Dong Qiaoxiang, Correa Liane M, VandeVoort Catherine A
California National Primate Research Center, University of California, Davis, CA, USA; School of Environmental Science and Public Health, Wenzhou Medical College, Wenzhou, China.
California National Primate Research Center, University of California, Davis, CA, USA.
Cryobiology. 2009 Feb;58(1):20-27. doi: 10.1016/j.cryobiol.2008.09.014. Epub 2008 Oct 21.
Recently, there has been increased interest in ultra-rapid freezing with mammalian spermatozoa, especially for vitrification in the absence of cryoprotectants. Sperm cryopreservation in non-human primates has been successful, but the use of frozen-thawed sperm in standard artificial insemination (AI) remains difficult, and removal of permeable cryoprotectant may offer opportunities for increased AI success. The present study intended to explore the possibility of freezing rhesus monkey sperm in the absence of permeable cryoprotectants. Specifically, we evaluated various factors such as presence or absence of egg yolk, the percentage of egg yolk in the extenders, and the effect of cooling and thawing rate on the success of freezing without permeable cryoprotectants. Findings revealed that freezing with TEST in the absence of egg yolk offers little protection (<15% post-thaw motility). Egg yolk of 40% or more in TEST resulted in decreased motility, while egg yolk in the range of 20-30% yielded the most motile sperm. Cooling at a slow rate (29 degrees C/min) reduced post-thaw motility significantly for samples frozen with TEST-yolk alone, but had no effect for controls in the presence of glycerol. Similarly, slow thawing in room temperature air is detrimental for freezing without permeable cryoprotectant (<2% motility). In addition to motility, the ability of sperm to capacitate based on an increase in intracellular calcium levels upon activation with cAMP and caffeine suggested no difference between fresh and frozen-thawed motile sperm, regardless of treatment. In summary, the present study demonstrates that ejaculated and epididymal sperm from rhesus monkeys can be cryopreserved with TEST-yolk (20%) in the absence of permeable cryoprotectant when samples were loaded in a standard 0.25-mL straw, cooled rapidly in liquid nitrogen vapor at 220 degrees C/min, and thawed rapidly in a 37 degrees C water bath. This study also represents the first success of freezing without permeable cryoprotectant in non-human primates.
最近,人们对用超快速冷冻法冷冻哺乳动物精子的兴趣日益增加,尤其是在无冷冻保护剂的情况下进行玻璃化冷冻。非人灵长类动物的精子冷冻保存已获成功,但在标准人工授精(AI)中使用冻融精子仍然困难,而去除可渗透的冷冻保护剂可能会提高人工授精的成功率。本研究旨在探索在无可渗透冷冻保护剂的情况下冷冻恒河猴精子的可能性。具体而言,我们评估了各种因素,如有无蛋黄、蛋黄在稀释液中的百分比,以及冷却和解冻速率对无可渗透冷冻保护剂冷冻成功率的影响。研究结果表明,在无蛋黄的情况下用TEST冷冻几乎没有保护作用(解冻后活力<15%)。TEST中蛋黄含量达到或超过40%会导致活力下降,而蛋黄含量在20%-30%范围内时精子活力最高。对于仅用TEST-蛋黄冷冻的样本,缓慢冷却速率(29℃/分钟)会显著降低解冻后活力,但对添加甘油的对照组没有影响。同样,在室温空气中缓慢解冻对无可渗透冷冻保护剂的冷冻是有害的(活力<2%)。除活力外,基于用cAMP和咖啡因激活后细胞内钙水平升高来判断精子的获能能力,结果表明新鲜和冻融后有活力的精子之间没有差异,无论处理方式如何。总之,本研究表明,当将样本装入标准的0.25毫升细管中,在液氮蒸汽中以220℃/分钟的速度快速冷却,并在37℃水浴中快速解冻时,恒河猴的射出精子和附睾精子可以在无可渗透冷冻保护剂的情况下用TEST-蛋黄(20%)进行冷冻保存。本研究也是非人灵长类动物在无可渗透冷冻保护剂情况下冷冻成功的首例。