Mirgalooye Bayat Sheida, Farzaneh Farahnaz, Mirgaloybayat Shahla
Department of Biology, Islamic Azad University Science and Research Branch, Tehran, Iran.
Department of Obstetrics and Gynecology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
J Reprod Infertil. 2024 Apr-Jun;25(2):148-156. doi: 10.18502/jri.v25i2.16009.
Freezing is a crucial technique in reproductive science utilized for the preservation of sperm samples. However, the process of freezing and thawing sperm can result in detrimental effects on sperm quality. One of the major mechanisms underlying this decline in sperm quality is the generation of reactive oxygen species during the freeze process. The purpose of the current study was to investigate the effects of magnesium oxide nanoparticles on frozen sperm parameters.
Semen samples were collected from 8 fertile men, aged 30 to 42 years, with normozoospermia, following 3 to 5 days of abstinence. The samples were divided into fresh (n=3), freeze (n=3), and control (n=2) groups. Three fresh experimental groups were only exposed to MgO NPs with concentrations of 5, 25, and 50 and three freezing experimental groups were frozen after being treated with MgO NPs, thawed, and analyzed after 30 .
Our findings revealed that the progressive movement and vitality of sperm experienced a significant decline, while non-progressive and immotile sperm showed a notable increase in both fresh and frozen experimental groups exposed to MgO NPs. However, the application of MgO NPs during fresh and freezing processes demonstrated an effective preservation of pH, morphology, and DNA fragmentation in sperm cells.
The analysis revealed that MgO NPs negatively impact sperm motility and viability in both fresh and freeze analysis. Also, the use of MgO NPs in fresh and frozen processes effectively maintains the pH, morphology, and fragmentation of DNA in sperm cells.
冷冻是生殖科学中用于保存精子样本的一项关键技术。然而,精子的冷冻和解冻过程可能会对精子质量产生不利影响。精子质量下降的主要机制之一是在冷冻过程中产生活性氧。本研究的目的是探讨氧化镁纳米颗粒对冷冻精子参数的影响。
从8名年龄在30至42岁、精子正常的健康男性中收集精液样本,禁欲3至5天。样本分为新鲜组(n = 3)、冷冻组(n = 3)和对照组(n = 2)。三个新鲜实验组仅暴露于浓度为5、25和50的氧化镁纳米颗粒,三个冷冻实验组在接受氧化镁纳米颗粒处理后进行冷冻,解冻后30分钟进行分析。
我们的研究结果表明,在暴露于氧化镁纳米颗粒的新鲜和冷冻实验组中,精子的前向运动和活力显著下降,而非前向和不动精子显著增加。然而,在新鲜和冷冻过程中应用氧化镁纳米颗粒显示出对精子细胞的pH值、形态和DNA片段化有有效的保存作用。
分析表明,氧化镁纳米颗粒在新鲜和冷冻分析中均对精子活力和生存能力有负面影响。此外,在新鲜和冷冻过程中使用氧化镁纳米颗粒可有效维持精子细胞的pH值、形态和DNA片段化。