Bolanos J R, Overstreet J W, Katz D F
Fertil Steril. 1983 Apr;39(4):536-41. doi: 10.1016/s0015-0282(16)46947-5.
The motility of human spermatozoa and their ability to penetrate zona-free hamster eggs were examined after dilution of the semen with TES-Tris (TEST) yolk buffer and storage for 48 hours at 2 degrees C to 5 degrees C. Semen samples from 10 fertile donors and 19 infertility patients were studied. More than 65% of the spermatozoa which were initially motile in the TEST yolk buffer remained active after storage. During storage, the mean swimming speed of the sperm declined to approximately 60% of the prestorage value. The percentage of zona-free hamster eggs that were penetrated by spermatozoa from patients and donors increased significantly following 48 hours of storage at 2 degrees C to 5 degrees C. Normal semen and abnormal semen were equally preserved by this storage method. This procedure may be used to ship semen samples by commercial transportation to specialized laboratories for testing. Low temperature storage in the TEST yolk buffer appears to enhance the fertilizing capacity of human spermatozoa in vitro.
用TES-三羟甲基氨基甲烷(TEST)卵黄缓冲液稀释精液并在2℃至5℃下储存48小时后,检测了人类精子的活力及其穿透去透明带仓鼠卵的能力。研究了来自10名有生育能力的供体和19名不育患者的精液样本。最初在TEST卵黄缓冲液中具有活力的精子中,超过65%在储存后仍保持活性。在储存期间,精子的平均游动速度降至储存前值的约60%。在2℃至5℃下储存48小时后,患者和供体的精子穿透去透明带仓鼠卵的百分比显著增加。正常精液和异常精液通过这种储存方法得到了同样好的保存。该程序可用于通过商业运输将精液样本运送至专业实验室进行检测。在TEST卵黄缓冲液中低温储存似乎能增强人类精子在体外的受精能力。