Karimi Zarchi Motahareh, Maleki Behnam, Dehghani Ashkezari Mahmood, Motamed Zadeh Leila, Agha-Rahimi Azam
Department of Biology, Medical Biotechnology Research Center, Ashkezar Branch, Islamic Azad University, Yazd, Iran.
Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
J Reprod Infertil. 2020 Oct-Dec;21(4):275-282. doi: 10.18502/jri.v21i4.4332.
Sperm quality is an important factor in assisted reproductive technology (ART) that affects the success rate of infertile couples treatment. incubation of sperm can influence its parameters and DNA integrity. The present study focused on the effect of different incubation temperatures sperm parameters on asthenoteratozoospermia semen prepared with density gradient centrifugation at different times.
Twenty-seven samples were collected and prepared. Then, the suspension was divided into two parts. One part was incubated at room temperature (RT), and another was incubated at 37°. Immediately and after 2 (2H) and 4 (4H), spermatozoa were evaluated regarding motility, viability, morphology, sperm protamine deficiency, chromatin and DNA fragmentation. Statistical analysis was performed using paired t-test and repeated measures. The p<0.05 was considered statistically significant.
Our results showed that following 2 and 4 of incubation at RT, sperm progressive motility and viability decreased significantly. Sperm DNA fragmentation increased significantly following 2 and 4 of incubation at RT and 37°. The Trend analysis confirmed that there were no significant differences between sperm parameters and DNA fragmentation after different times at RT and 37°.
Incubation of sperm at RT in comparison to 37° didn't preserve sperm parameters and DNA efficiently. Therefore, IVF, ICSI and IUI procedure should be performed in the soonest possible time after sperm preparation.
精子质量是辅助生殖技术(ART)中的一个重要因素,会影响不孕夫妇治疗的成功率。精子孵育会影响其参数和DNA完整性。本研究聚焦于不同孵育温度对经密度梯度离心法在不同时间制备的弱畸精子症精液的精子参数的影响。
收集并制备27份样本。然后,将悬浮液分成两部分。一部分在室温(RT)下孵育,另一部分在37°下孵育。在即刻、2小时(2H)和4小时(4H)后,对精子的活力、存活率、形态、精子鱼精蛋白缺乏、染色质和DNA片段化进行评估。使用配对t检验和重复测量进行统计分析。p<0.05被认为具有统计学意义。
我们的结果表明,在室温下孵育2小时和4小时后,精子的前向运动能力和存活率显著下降。在室温下和37°孵育2小时和4小时后,精子DNA片段化显著增加。趋势分析证实,在室温下和37°不同时间后,精子参数和DNA片段化之间没有显著差异。
与37°相比,在室温下孵育精子不能有效地保持精子参数和DNA。因此,体外受精、卵胞浆内单精子注射和宫腔内人工授精程序应在精子制备后尽快进行。