Beigi Sayed Abbas Datli, Khalili Mohammad Ali, Nabi Ali, Hosseini Mohammad, Sarcheshmeh Abolghasem Abbasi, Sabour Mojdeh
Abortion Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Andrology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Clin Exp Reprod Med. 2022 Dec;49(4):270-276. doi: 10.5653/cerm.2022.05435. Epub 2022 Nov 7.
The present study assessed the biological characteristics of human spermatozoa at different time intervals (0, 1, 1.5, and 2 hours) after incubation at 37°C.
Twenty-five normozoospermic semen samples were incubated at 37°C. Incubation was performed at four time intervals of 0 (after liquefaction), 1, 1.5, and 2 hours. The samples were evaluated for sperm parameters at each time interval.
The rate of sperm progressive motility decreased at 1.5 hours compared to 0 hours as well as 2 hours compared to 1 hour and 0 hours. The rate of non-motile spermatozoa also decreased after 2 hours compared to after 0 hours. No significant changes were observed in sperm viability (p=0.98) and non- progressive motility (p=0.48) at any time intervals. Abnormal sperm morphology increased at 1.5 hours of incubation time (p<0.001). No significant changes were observed in DNA fragmentation at 1 hour compared to 0 hours (median [interquartile range]: 19.5 [4] vs. 19 [4]), as well as at 1.5 hours compared to 1 hour (20 [5]). However, a significant increase in DNA fragmentation was observed at 1.5 hours compared to 0 hours. The mitochondrial membrane potential decreased remarkably after 1 hour of incubation time. No significant differences were observed in the acrosome reaction or malonaldehyde levels at any time point (p=0.34 and p=0.98, respectively).
The incubation of normozoospermic samples before use in assisted reproductive technology should be less than 1.5 hours to minimize the destructive effects of prolonged incubation time on general and specific sperm parameters.
本研究评估了人类精子在37°C孵育不同时间间隔(0、1、1.5和2小时)后的生物学特性。
将25份正常精子精液样本在37°C下孵育。在0(液化后)、1、1.5和2小时这四个时间间隔进行孵育。在每个时间间隔对样本的精子参数进行评估。
与0小时相比,1.5小时时精子前向运动率下降,与1小时和0小时相比,2小时时精子前向运动率也下降。与0小时后相比,2小时后不活动精子的比例也下降。在任何时间间隔,精子活力(p = 0.98)和非前向运动(p = 0.48)均未观察到显著变化。孵育1.5小时时异常精子形态增加(p<0.001)。与0小时相比,1小时时DNA碎片率无显著变化(中位数[四分位间距]:19.5 [4] 对 19 [4]),与1小时相比,1.5小时时也无显著变化(20 [5])。然而,与0小时相比,1.5小时时DNA碎片率显著增加。孵育1小时后线粒体膜电位显著下降。在任何时间点,顶体反应或丙二醛水平均未观察到显著差异(分别为p = 0.34和p = 0.98)。
在辅助生殖技术中使用前,正常精子样本的孵育时间应少于1.5小时,以尽量减少长时间孵育对精子一般和特定参数的破坏作用。