Küçük Niyazi
Department of Reproduction and Artificial Insemination, Adnan Menderes University Faculty of Veterinary Medicine, Aydın, Turkey.
Turk J Urol. 2018 Jan;44(1):1-5. doi: 10.5152/tud.2018.49321. Epub 2018 Jan 8.
The questionable effectiveness of routine sperm parameters in determining male factor infertility problems and increasing the success rates of assisted reproductive techniques have led to the investigation of more detailed sperm parameters that could affect the male fertility and reproduction. Thus, the effects of different sperm parameters such as sperm DNA integrity was started to be investigated thanks to the previously described methods such as single cell gel electrophoresis (COMET) assay, sperm chromatin structure assay (SCSA), acridine orange test (AOT), terminal deoxynucleotidyl transferase-mediated deoxyuridine (TdT) triphosphate (dUTP) nick end labeling (TUNEL) assay and sperm chromatin dispersion (SCD) test. However, studying on sperm DNA might be very complex because the sperm DNA differs from the somatic cell DNA with its unique structure. Also, the sperm DNA undergoes many changes during spermatogenesis and it is condensed by being packaged tightly with different types and numbers of protamines in different species. Despite all these difficulties, these methods provide important information about the reasons and consequences of DNA damages in sperm and the effects of these damages on reproduction.
常规精子参数在确定男性因素不育问题及提高辅助生殖技术成功率方面的效果存疑,这促使人们对可能影响男性生育和生殖的更详细精子参数展开研究。因此,借助此前描述的方法,如单细胞凝胶电泳(彗星)试验、精子染色质结构分析(SCSA)、吖啶橙试验(AOT)、末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸(dUTP)缺口末端标记(TUNEL)试验和精子染色质扩散(SCD)试验,开始研究不同精子参数的影响,如精子DNA完整性。然而,研究精子DNA可能非常复杂,因为精子DNA的独特结构使其不同于体细胞DNA。此外,精子DNA在精子发生过程中会经历许多变化,并且在不同物种中,它通过与不同类型和数量的鱼精蛋白紧密包装而浓缩。尽管存在所有这些困难,但这些方法提供了有关精子DNA损伤的原因和后果以及这些损伤对生殖影响的重要信息。