长时间的精液孵育改变了人类精子的生物学特性。

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY
Sayed Abbas Datli Beigi, Mohammad Ali Khalili, Ali Nabi, Mohammad Hosseini, Abolghasem Abbasi Sarcheshmeh, Mojdeh Sabour
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引用次数: 0

摘要

目的:本研究评估人精子在37℃孵育后不同时间间隔(0、1、1.5和2小时)的生物学特性。方法:取25份正常精子标本,37℃孵育。孵育时间间隔为0(液化后)、1、1.5和2小时。在每个时间间隔对样本进行精子参数评估。结果:与0小时相比,1.5小时精子进行性运动率下降;与1小时和0小时相比,2小时精子进行性运动率下降。与0小时相比,2小时后无运动精子的比例也有所下降。在任何时间间隔内,精子活力(p=0.98)和非进行性运动(p=0.48)均无显著变化。结论:在辅助生殖技术使用前,正常精子样品的孵育时间应少于1.5小时,以尽量减少孵育时间延长对精子一般和特定参数的破坏性影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prolonged semen incubation alters the biological characteristics of human spermatozoa.

Prolonged semen incubation alters the biological characteristics of human spermatozoa.

Prolonged semen incubation alters the biological characteristics of human spermatozoa.

Prolonged semen incubation alters the biological characteristics of human spermatozoa.

Objective: 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.

Methods: 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.

Results: 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).

Conclusion: 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.

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CiteScore
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