Toyonaga Mari, Sato Yuuka, Morita Miki, Watanabe Masashi, Oba Hiromichi, Mizutani Tatsuji, Hori Tatsuya, Tsutsui Toshihiko
Department of Reproduction, Nippon Veterinary and Life Science University, Japan.
J Vet Med Sci. 2010 Jun;72(6):777-80. doi: 10.1292/jvms.09-0260. Epub 2010 Jan 22.
We observed the influences of low-temperature storage of the feline epididymis on the epididymal semen qualities before and after cryopreservation to identify the optimal duration for low-temperature storage of the epididymis. After excision, the feline epididymis was stored at 4 degrees C for 0-72 hr and then subjected to epididymal sperm collection. When sperm from the refrigerated cauda epididymis were frozen and thawed, there was no significant difference in sperm motility between the 0- and 24-hr low-temperature storage groups, but sperm motility was significantly decreased in the 48-hr storage group. The above findings suggested that low-temperature storage of the epididymis until 24 hr is useful for frozen sperm collected from the feline cauda epididymis.
我们观察了猫附睾低温保存对冷冻保存前后附睾精液质量的影响,以确定附睾低温保存的最佳时长。切除后,将猫附睾在4℃下保存0至72小时,然后进行附睾精子采集。当冷冻和解冻来自冷藏附睾尾部的精子时,0小时和24小时低温保存组之间的精子活力没有显著差异,但48小时保存组的精子活力显著下降。上述结果表明,将附睾低温保存至24小时对从猫附睾尾部采集的冷冻精子是有效的。