Bwanga C O, Einarsson S, Rodriguez-Martinez H
Department of Obstetrics and Gynaecology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, Uppsala.
Acta Vet Scand. 1991;32(4):455-61. doi: 10.1186/BF03546945.
The post-thaw motility and the acrosome integrity of semen from 4 boars frozen with a programmable freezing machine, in mini (0.25 ml) and maxi (5 ml) plastic straws and in 10 x 5 cm Teflon FEP-plastic bags (0.12 mm thick, 5 ml), were compared. The freezing of the semen was monitored by way of thermo-couples placed in the straws and the bags. Three freezing programmes were used, namely A: from +5 degrees C, at a rate of 3 degrees C/min, to -6 degrees C, held for 1 min at -6 degrees C, and followed by a cooling rate of 20 degrees C/min to -100 degrees C; B: a similar curve except that there was no holding time at -6 degrees C and that the cooling rate was 30 degrees C/min, and C: from +5 degrees C to -100 degrees C, with a cooling rate of 35 degrees C/min, followed by storage in liquid N2. Despite the freezing curve assayed, both the mini-straws and the bags depicted much shorter freezing point plateaus as compared to the maxi-straws. Post-thaw sperm motility as well as the amount of normal apical ridges were equally significantly higher when semen was frozen in mini-straws or in bags than in maxi-straws. Significant differences in these post-thawing parameters were obtained between the freezing curves used. The stepwise freezing procedure A appeared as the best alternative for boar semen, considering this in vitro evaluation.
比较了用程序降温冷冻机冷冻的4头公猪精液在小型(0.25毫升)和大型(5毫升)塑料细管以及10×5厘米聚四氟乙烯FEP塑料袋(厚0.12毫米,5毫升)中的解冻后活力和顶体完整性。精液冷冻过程通过置于细管和袋子中的热电偶进行监测。使用了三种冷冻程序,即A:从+5℃以3℃/分钟的速率降至-6℃,在-6℃保持1分钟,然后以20℃/分钟的冷却速率降至-100℃;B:类似的曲线,但在-6℃没有保持时间,冷却速率为30℃/分钟;C:从+5℃降至-100℃,冷却速率为35℃/分钟,然后储存在液氮中。尽管测定了冷冻曲线,但与大型细管相比,小型细管和袋子的冷冻平台期都短得多。当精液在小型细管或袋子中冷冻时,解冻后精子活力以及正常顶嵴数量均显著高于在大型细管中冷冻的情况。在所使用的冷冻曲线之间,这些解冻后参数存在显著差异。从这种体外评估来看,逐步冷冻程序A似乎是公猪精液的最佳选择。