Garcia-Segura Sergio, Ribas-Maynou Jordi, Lara-Cerrillo Sandra, Garcia-Peiró Agustín, Castel Ana Belén, Benet Jordi, Oliver-Bonet Maria
Unit of Cell Biology and Medical Genetics, Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Av. Can Domenech s/n, Bellaterra, 08193 Catalunya, Spain.
CIMAB, Barcelona Male Infertility Centre, C. Vallcorba 1-3, Sant Quirze del Vallès, 08192 Catalunya, Spain.
Biology (Basel). 2020 Sep 1;9(9):262. doi: 10.3390/biology9090262.
Seminal oxidative stress (OS) is one of the most promising factors to describe the causes of idiopathic male infertility. Redox balance is essential in several biological processes related to fertility, so alterations such as high reactive oxygen species (ROS) levels or low antioxidant agent levels can compromise it. MiOXSYS has been developed to evaluate the seminal static oxidation-reduction potential (sORP) and it has been proposed as an effective diagnostic biomarker. However, its relationship with parameters like sperm DNA fragmentation (SDF), chromatin compaction status or seminal pH requires further analysis, making it the object of this study. Semen and sORP analysis were performed for all samples. A terminal deoxynucleotidyl transferase dUTP nick end labeling assay (TUNEL) and Comet assay were used to assess SDF and chromomycin a3 (CMA3) test to assess sperm chromatin compaction. Regarding sORP measures, it was found that alkaline pH has an effect on sample reproducibility. To our knowledge, this unexpected effect has not been previously described. A statistical analysis showed that sORP correlated negatively with CMA3 positive cells and sperm motility, but not with SDF. As redox dysregulation, which occurs mainly at the testicular and epididymal level, causes chromatin compaction problems and leaves DNA exposed to damage, an excess of ROS could be counterbalanced further by a seminal supply of antioxidant molecules, explaining the negative correlation with CMA3 positive cells but no correlation with SDF. Our results show that the study of idiopathic infertility would benefit from a combined approach comprising OS analysis, SDF and chromatin compaction analysis.
精液氧化应激(OS)是描述特发性男性不育原因最具潜力的因素之一。氧化还原平衡在与生育相关的多个生物学过程中至关重要,因此诸如高活性氧(ROS)水平或低抗氧化剂水平等改变可能会破坏这种平衡。MiOXSYS已被开发用于评估精液静态氧化还原电位(sORP),并已被提议作为一种有效的诊断生物标志物。然而,它与精子DNA碎片化(SDF)、染色质压实状态或精液pH值等参数的关系需要进一步分析,这使其成为本研究的对象。对所有样本进行了精液和sORP分析。采用末端脱氧核苷酸转移酶dUTP缺口末端标记法(TUNEL)和彗星试验评估SDF,采用嗜铬霉素A3(CMA3)试验评估精子染色质压实情况。关于sORP测量,发现碱性pH值对样本的可重复性有影响。据我们所知,这种意外影响此前尚未有过描述。统计分析表明,sORP与CMA3阳性细胞和精子活力呈负相关,但与SDF无关。由于主要在睾丸和附睾水平发生的氧化还原失调会导致染色质压实问题并使DNA暴露于损伤中,精液中抗氧化分子的供应可能会进一步抵消过量的ROS,这解释了sORP与CMA3阳性细胞呈负相关但与SDF无相关性。我们的结果表明,特发性不育的研究将受益于一种综合方法,包括OS分析、SDF和染色质压实分析。