Tunc Ozlem, Thompson Jeremy, Tremellen Kelton
Discipline of Obstetrics and Gynaecology, University of Adelaide, South Australia.
Reprod Biomed Online. 2009 Jun;18(6):761-8. doi: 10.1016/s1472-6483(10)60024-7.
Oxidative stress is now recognized as a common pathology that affects up to half of all infertile men. One of the principal mechanisms by which oxidative stress produces infertility is by damage to sperm DNA, either through direct oxidation of the DNA by reactive oxygen species (ROS) or by the initiation of apoptosis. The objective of this study was to determine if an oral antioxidant/mineral supplement could improve sperm DNA integrity in men with known oxidative stress. A total of 50 infertile men identified as exhibiting oxidative stress were administered oral antioxidant therapy for a period of 3 months. All participants were assessed at entry and exit for sperm DNA integrity with terminal deoxynucleotidyl transferase-mediated dUDP nick-end labelling, apoptosis with annexin V, protamination with chromomycin A(3) and ROS production with nitro blue tetrazolium assay. Sperm concentration, motility and morphology, together with assessment of serum male reproductive hormones (LH, FSH, testosterone, anti-Mullerian hormone), were also monitored. The principal finding that emerged from this study was that antioxidant therapy resulted in significant improvements in sperm DNA integrity (P = 0.002) and protamine packaging (P < 0.001), accompanied by a reduction in seminal ROS production (P = 0.027) and apoptosis (P = 0.004). No significant changes in routine sperm parameters (concentration, motility, morphology) or male reproductive hormones were observed.
氧化应激现已被公认为一种常见的病理状态,影响着多达一半的不育男性。氧化应激导致不育的主要机制之一是通过活性氧(ROS)直接氧化DNA或引发细胞凋亡来损害精子DNA。本研究的目的是确定口服抗氧化剂/矿物质补充剂是否能改善已知存在氧化应激的男性的精子DNA完整性。共有50名被确定表现出氧化应激的不育男性接受了为期3个月的口服抗氧化剂治疗。所有参与者在入组和出组时均通过末端脱氧核苷酸转移酶介导的dUDP缺口末端标记法评估精子DNA完整性,通过膜联蛋白V评估细胞凋亡,通过放线菌素A(3)评估鱼精蛋白化,通过硝基蓝四唑试验评估ROS产生。还监测了精子浓度、活力和形态,以及血清男性生殖激素(促黄体生成素、促卵泡生成素、睾酮、抗苗勒管激素)的评估。本研究得出的主要发现是,抗氧化剂治疗导致精子DNA完整性(P = 0.002)和鱼精蛋白包装(P < 0.001)显著改善,同时精液ROS产生(P = 0.027)和细胞凋亡(P = 0.004)减少。未观察到常规精子参数(浓度、活力、形态)或男性生殖激素有显著变化。