Zavos P M, Correa J R, Zarmakoupis P N
Department of Animal Science, University of Kentucky, Lexington 40523, USA.
Tohoku J Exp Med. 1995 Feb;175(2):101-9. doi: 10.1620/tjem.175.101.
This study was designed to determine the effects of Sephadex filtration (SpermPrep method) on the separation of viable motile, morphologically normal mouse epididymal spermatozoa and to study the viability of the recovered spermatozoa over a 3 hr incubation period. Spermatozoa were harvested from the caudae epididymides (5 animals per run or replication; n = 10) following bilateral testicular excision and incubated in 2-ml of Test-Yolk buffer (TYB) at 37 degrees C for 15 min. The specimen was then split into 2 aliquots, with Alquot 1 as the control and Aliquot 2 used for filtration. SpermPrep I column was employed according to the manufacturer's specifications (ZBL, Inc., Lexington, KY, USA) using TYB. During filtration (10 min), different fractions were obtained: first 5 min (Sample 1) and second 5 min (Sample 2). The filtered fractions were evaluated and incubated at 37 degrees C and assessed for percentage and grade of motility (0-4) every 30 min for 3 hr. Filtration resulted in a significant improvement in percentage and grade of motility (91.5% and 3.0 vs. 76.5% and 2.5, respectively). The results point out very clearly that the filtration via the SpermPrep method improved the percentage and grade of motility (p < 0.05) but not the percentage normal morphology of the spermatozoa. Also the SpermPrep I enabled the recovery of 45% (8.3 x 10(6) spermatozoa) of the total spermatozoa processed in the control aliquot (18.4 x 10(6) spermatozoa) which is consistent with previous observations. Most importantly, filtered spermatozoa incubated for 3 hr showed greater percentage and grade of motility than the control spermatozoa (63% and 1.66 vs. 39% and 0.82, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在确定葡聚糖凝胶过滤法(精子制备法)对活力良好、形态正常的小鼠附睾精子分离的影响,并研究回收精子在3小时孵育期内的活力。双侧睾丸切除后,从附睾尾部采集精子(每次实验或重复5只动物;n = 10),并在37℃下于2ml的试验-卵黄缓冲液(TYB)中孵育15分钟。然后将样本分成2等份,其中等份1作为对照,等份2用于过滤。按照制造商的规格(美国肯塔基州列克星敦市的ZBL公司)使用TYB,采用精子制备I柱。在过滤过程中(10分钟),获得了不同的组分:前5分钟(样本1)和后5分钟(样本2)。对过滤后的组分进行评估,并在37℃下孵育,每30分钟评估一次活力百分比和等级(0-4级),共评估3小时。过滤后活力百分比和等级显著提高(分别为91.5%和3.0级,而之前为76.5%和2.5级)。结果非常清楚地表明,通过精子制备法过滤提高了活力百分比和等级(p < 0.05),但未提高精子正常形态的百分比。此外,精子制备I柱能够回收对照等份中处理的总精子的45%(8.3×10⁶个精子)(18.4×10⁶个精子),这与之前的观察结果一致。最重要的是,孵育3小时的过滤精子比对照精子显示出更高的活力百分比和等级(分别为63%和1.66级,而对照为39%和0.82级)。(摘要截断于250字)