Yusuf Ilyas, Emokpae Mathias Abiodun
Department of Medical Laboratory Science, School of Basic Medical Sciences, College of Medical Sciences, University of Benin, Benin City, Nigeria.
Int J Reprod Biomed. 2021 Feb 21;19(2):137-146. doi: 10.18502/ijrm.v19i2.8472. eCollection 2021 Feb.
Studies have shown oxidative DNA damage is associated with male infertility.
This study determines the levels of 8-hydroxy-2'-deoxyguanosine (8-OHdG) and some markers of oxidative stress in seminal fluid of males investigated for infertility and men of proven fertility in Benin City, Nigeria.
Semen samples produced by self or assisted masturbation were analyzed by microscopic technique according to the World Health Organization guidelines. Thereafter, samples were centrifuged and seminal fluid plasma separated and stored at -20°C prior to assay for 8-OHdG and oxidative stress biomarkers. Based on the sperm concentration/count, the overall samples were grouped into the following categories: normospermia (n = 20), oligozoospermia (n = 30), and azoospermia (n = 20). The control group comprised of 30 age-matched males of proven fertility. The seminal fluid 8-OHdG, total antioxidant status, superoxide dismutase and malondialdehyde (MDA) were assayed through ELISA and spectrophotometric methods, respectively.
Seminal plasma level of 8-OHdG and MDA were significantly higher (p = 0.01) in infertile subjects than controls. The mean levels of 8-OHdG and MDA in infertile subjects were higher in azoospermia than oligospermia than normospermia and so, was least in the normospermia. Conversely, the mean levels of total antioxidant status and superoxide dismutase were significantly lower (p = 0.01) in infertile than fertile the control male subjects with levels higher in normospermia than oligospermia and least in azoospermia. Moreover, the seminal 8-OHdG correlated negatively with sperm count (r = -0.359, p = 0.01), percent motility (r = -0.388, p = 0.04), and percent morphology (r = -0.327, p = 0.02).
The assessment of sperm DNA damage in addition to routine seminal fluid analysis may play an important role in specific diagnosis and management of male infertility.
研究表明,氧化性DNA损伤与男性不育有关。
本研究测定了尼日利亚贝宁城因不育接受调查的男性以及已证实具有生育能力的男性精液中8-羟基-2'-脱氧鸟苷(8-OHdG)的水平和一些氧化应激标志物。
按照世界卫生组织指南,采用显微镜技术对通过手淫或辅助手淫采集的精液样本进行分析。之后,将样本离心,分离出精液血浆,在-20°C下保存,用于检测8-OHdG和氧化应激生物标志物。根据精子浓度/计数,将所有样本分为以下几类:正常精子症(n = 20)、少精子症(n = 30)和无精子症(n = 20)。对照组由30名年龄匹配的已证实具有生育能力的男性组成。分别通过酶联免疫吸附测定法(ELISA)和分光光度法检测精液中的8-OHdG、总抗氧化状态、超氧化物歧化酶和丙二醛(MDA)。
不育受试者精液血浆中8-OHdG和MDA的水平显著高于对照组(p = 0.01)。不育受试者中,无精子症患者的8-OHdG和MDA平均水平高于少精子症患者,少精子症患者高于正常精子症患者,正常精子症患者的水平最低。相反,不育男性受试者的总抗氧化状态和超氧化物歧化酶平均水平显著低于有生育能力的对照男性受试者(p = 0.01),正常精子症患者的水平高于少精子症患者,无精子症患者的水平最低。此外,精液中的8-OHdG与精子计数(r = -0.359,p = 0.01)、活动率百分比(r = -0.388,p = 0.04)和形态学百分比(r = -0.327,p = 0.02)呈负相关。
除了常规精液分析外,评估精子DNA损伤可能在男性不育的特异性诊断和管理中发挥重要作用。