精子DNA断裂(SDF)与活性氧(ROS)引起的男性不育相关的临床指南

Mustafa Zakaria, Aya Al-ibraheemi, M. Ennaji, W. Senhaji, A. Natiq, Romaissa Boutiche, M. Mbaye, M. Zarqaoui, M. Hassan, Hayder A. Mossa, N. Louanjli
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引用次数: 0

摘要

精子DNA断裂在不育男性中很常见。此外,精子DNA的完整性对受精和后代的健康发育至关重要。许多遗传和环境因素对精子DNA完整性产生负面影响。比如生活方式、衰老、工业毒素和感染。SDF的机制多种多样,但细胞凋亡和活性氧被认为是SDF的主要机制。男性不育症的治疗导致了对更先进的SDF诊断工具来诊断精子DNA的渴望。许多精子DNA损伤检测,如末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸镍端标记(TUNEL)检测和原位缺口翻译(非原位缺口翻译)可用于提高SDF的诊断和最终更好的SDF管理。临床SDF可导致妊娠率低、胚胎发育缺陷和后代健康受损。此外,SDF可以通过体外受精或胞浆内单精子注射将基因转移到胚胎中来影响辅助生殖技术的有效性。SDF可以通过改变生活方式、治疗男性生殖道感染和活性氧来控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Guidelines for Sperm DNA Fragmentation (SDF) is Associated with Male Infertility from Reactive Oxygen Species (ROS)
Sperm DNA fragmentation is common in infertile male. Besides, sperm DNA integrity is essential for fertilization and healthy offspring development. Numerous genetic and environmental elements are associated with impacting sperm DNA integrity negatively. Such as lifestyle, ageing, industrial toxins, and infection. The mechanisms behind SDF are many, but apoptosis and reactive oxygen species are considered the main SDF mechanisms. The management of male infertility has led to the desire for more advanced SDF diagnostic tools to diagnose sperm DNA. Numerous sperm DNA damage assays such as terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labelling (TUNEL) assay and in situ nick translation (ISNT) are available to enhance SDF diagnosing and ultimately to better SDF management. Clinical SDF can lead to a low pregnancy rate, defects in embryo development and impaired offspring health. Moreover, SDF can impact the effectiveness of assisted reproductive technology through transfer genetics impartment to the embryo b in vitro fertilization or intracytoplasmic sperm injection. SDF can be mange through lifestyle changing, treating existing infection in the male reproductive tract and reactive oxygen species.
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