Ghafarizadeh A A, Vaezi G, Shariatzadeh M A, Malekirad A A
Department of Biology, Faculty of Science, Damghan Branch, Islamic Azad University, Damghan, Iran.
Infertility Center, Iranian Academic Center for Education, Culture & Research (ACECR), Arak, Iran.
Andrologia. 2018 Mar;50(2). doi: 10.1111/and.12869. Epub 2017 Aug 6.
Sperm DNA damage, excessive oxidative stress and decrease in motility may lead to low fertilisation or poor assisted reproductive techniques outcomes in asthenoteratozoospermic men. Selenium was considered as essential element for male reproductive functions. Selenium has important role in enzymatic process for elimination of excessive reactive oxygen species and helps to maintain membrane integrity. The aim of this study was to determine the effect of selenium supplementation on sperm quality, DNA fragmentation, mitochondrial membrane potential and membrane lipid peroxidation during sperm sampling in vitro at different times. In this experimental study, semen samples were collected from 50 asthenoteratozoospermic men. Samples were divided into two groups as control group and test group (incubated with 2 μg/ml selenium at 37°C for 2, 4 and 6 hr). Motility and viability were assessed based on WHO 2010 criteria. Mitochondrial membrane potential, sperm DNA fragmentation and malondialdehyde levels were evaluated in each group. Results revealed that motility, viability and mitochondrial membrane potential were significantly higher in the test group (p < .05). Also malondialdehyde levels were significantly lower in the test group (p < .03). DNA fragmentation significantly decreased in the test group after 6 hr of incubation (p < .02). In conclusion, in vitro selenium supplementation may protect spermatozoa from maltreatment effect of reactive oxygen species (ROS) during sperm sampling via keeping enzymatic and antioxidant process in optimum condition.
精子DNA损伤、过度氧化应激和活力下降可能导致弱畸精子症男性受精率低或辅助生殖技术效果不佳。硒被认为是男性生殖功能的必需元素。硒在消除过量活性氧的酶促过程中起重要作用,并有助于维持膜的完整性。本研究的目的是确定在体外不同时间采集精子过程中补充硒对精子质量、DNA片段化、线粒体膜电位和膜脂质过氧化的影响。在这项实验研究中,从50名弱畸精子症男性中采集精液样本。样本分为对照组和试验组(在37°C下与2μg/ml硒孵育2、4和6小时)。根据世界卫生组织2010年标准评估活力和存活率。评估每组的线粒体膜电位、精子DNA片段化和丙二醛水平。结果显示,试验组的活力、存活率和线粒体膜电位显著更高(p<0.05)。试验组的丙二醛水平也显著更低(p<0.03)。孵育6小时后,试验组的DNA片段化显著降低(p<0.02)。总之,体外补充硒可能通过使酶促和抗氧化过程保持在最佳状态,在精子采集过程中保护精子免受活性氧(ROS)的不良影响。