Atig Fatma, Kerkeni Abdelhamid, Saad Ali, Ajina Mounir
Unit of Reproductive Medicine, University Farhat Hached Hospital, 4000, Soussa, Tunisia.
Department of Cytogenetic and Reproductive Biology, University Farhat Hached Hospital, 4000, Soussa, Tunisia.
J Assist Reprod Genet. 2017 Mar;34(3):373-381. doi: 10.1007/s10815-013-9936-x. Epub 2013 Jan 25.
To evaluate levels of sperm DNA fragmentation and enzymatic antioxidant status in seminal plasma of Tunisian fertile and infertile men in order to assess the effects of seminal oxidative stress on sperm DNA integrity and semen quality.
Semen samples from 100 infertile patients (40 oligoasthenoteratozoospermics, 31 teratozoospermics and 29 asthenozoospermics) and 50 fertile men (controls) were analyzed for DNA fragmentation by TUNEL assay and biochemical parameters. Seminal antioxidant activities (Superoxide dismutase, Glutathione peroxidase and Catalase) and malondialdehyde concentrations were measured spectrophotometrically.
Sperm DNA fragmentation and malondialdehyde levels in infertile groups were more elevated than controls. Nevertheless, the activities of the antioxidant enzymes were significantly lower in abnormal groups compared to normozoospermics. Sperm DNA fragmentation was closely and positively correlated to malondialdehyde levels (r = 0.37, P = 0.008); meanwhile, reduced seminal antioxidant profile was negatively associated to sperm DNA fragmentation. Interestingly, we noted also that sperm DNA fragmentation was negatively correlated to sperm motility (r = -0.54, P < 0.001) and positively associated to the abnormal sperm morphology (r = 0.57, P = 0.002).
This report revealed that increased sperm DNA fragmentation can be due to the impaired seminal enzymatic antioxidant profile and increased Lipid peroxidation. Our results sustain that the evaluation of sperm DNA fragmentation and seminal oxidative biomarkers in infertile men is recommended as a consistent prognostic tool for male infertility assessment.
评估突尼斯生育男性和不育男性精液中精子DNA片段化水平及酶促抗氧化状态,以评估精液氧化应激对精子DNA完整性和精液质量的影响。
对100例不育患者(40例少弱畸精子症患者、31例畸精子症患者和29例弱精子症患者)和50例生育男性(对照组)的精液样本进行TUNEL检测分析DNA片段化情况及生化参数。采用分光光度法测定精液抗氧化活性(超氧化物歧化酶、谷胱甘肽过氧化物酶和过氧化氢酶)和丙二醛浓度。
不育组的精子DNA片段化水平和丙二醛水平高于对照组。然而,与正常精子组相比,异常组的抗氧化酶活性显著降低。精子DNA片段化与丙二醛水平密切正相关(r = 0.37,P = 0.008);同时,精液抗氧化指标降低与精子DNA片段化呈负相关。有趣的是,我们还注意到精子DNA片段化与精子活力呈负相关(r = -0.54,P < 0.001),与异常精子形态呈正相关(r = 0.57,P = 0.002)。
本报告显示精子DNA片段化增加可能是由于精液酶促抗氧化指标受损和脂质过氧化增加所致。我们的结果支持,对不育男性进行精子DNA片段化和精液氧化生物标志物评估,作为男性不育评估的一种可靠预后工具是值得推荐的。