Gamzu R, Yogev L, Yavetz H, Homonnai Z T, Hiss Y, Paz G
Institute for the Study of Fertility, Serlin Maternity Hospital, Tel Aviv, Israel.
Fertil Steril. 1992 Dec;58(6):1254-6. doi: 10.1016/s0015-0282(16)55582-4.
This study evaluated the impact of sperm cryopreservation on sperm quality. The HZA was used to test the binding capacity of fresh as opposed to frozen-thawed sperm from 12 donors. Fresh and frozen-thawed sperm motility was 47% +/- 1.5% and 24% +/- 3.8% (mean +/- SE), respectively. However, the number of sperm cells attached to the hemizonae was 75 +/- 12.0 and 74 +/- 11.9, respectively. We conclude that cryopreservation results in a reduced number of motile sperm cells but does not adversely affect the ability of rescued sperm cells to bind to the ZP. The study also supports the use of frozen-thawed rather than fresh donor sperm for control in the HZA procedure.
本研究评估了精子冷冻保存对精子质量的影响。采用半透明带分析法(HZA)检测了12名供体的新鲜精子与冻融精子的结合能力。新鲜精子和冻融精子的活力分别为47%±1.5%和24%±3.8%(平均值±标准误)。然而,附着在半透明带上的精子细胞数量分别为75±12.0和74±11.9。我们得出结论,冷冻保存会导致活动精子细胞数量减少,但不会对获救精子细胞与透明带(ZP)结合的能力产生不利影响。该研究还支持在HZA程序中使用冻融而非新鲜供体精子作为对照。