Zini A, Schlegel P N
James Buchanan Brady Foundation, Department of Urology, New York Hospital-Cornell Medical Center, NY 10021, USA.
J Urol. 1997 Aug;158(2):659-63.
The testis is known to be highly sensitive to a number of physical stresses. Previous investigations suggest that oxidative stress may be an important mediator of testicular injury. The ability of the testis to manage oxidative stress may be limited by enzymatic clearance of reactive oxygen species (ROS). To evaluate the ability of the testis to withstand the common pathologic conditions of cryptorchidism and obstruction, we measured mRNA levels of testicular antioxidant enzymes. Prepubertal rats were rendered unilaterally cryptorchid and 40 days after the procedure, cryptorchid, contralateral and control (sham) testes were harvested for RNA extraction. Adult rats were subjected to unilateral efferent duct ligation and the obstructed testes harvested 1 to 28 days after the procedure. Antioxidant enzyme mRNA expression was assessed by Northern blot analysis using 32P-labeled DNA probes for classical cellular glutathione peroxidase (GSHPx), phospholipid hydroperoxide glutathione peroxidase (PHGPX), Cu/Zn superoxide dismutase (SOD) and catalase. In both cryptorchid and contralateral testes, the germ cell-specific 0.9 kb SOD and PHGPX mRNA transcript levels were significantly decreased compared to control testes (p < 0.05). Similarly, after efferent duct ligation, the 0.9 kb SOD and PHGPX mRNA transcript levels also decreased compared to control testes (p < 0.05). These findings suggest that the overall decline in testicular mRNA transcript levels after efferent duct ligation and cryptorchidism is primarily due to germ cell depletion. Reduced levels of antioxidant enzyme mRNAs in cryptorchid testes have been documented. Further experiments may elucidate the role of increased oxidative stress associated with decreased antioxidants in cryptorchidism. It remains to be determined whether oxidative stress has a causative role in the abnormal spermatogenesis and tumorigenesis associated with cryptorchidism.
已知睾丸对多种物理应激高度敏感。先前的研究表明,氧化应激可能是睾丸损伤的重要介质。睾丸处理氧化应激的能力可能受活性氧(ROS)酶促清除的限制。为了评估睾丸抵抗隐睾症和梗阻等常见病理状况的能力,我们测量了睾丸抗氧化酶的mRNA水平。对青春期前大鼠进行单侧隐睾手术,术后40天,采集隐睾、对侧和对照(假手术)睾丸用于RNA提取。对成年大鼠进行单侧输出小管结扎,并在术后1至28天采集梗阻睾丸。使用针对经典细胞谷胱甘肽过氧化物酶(GSHPx)、磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPX)、铜/锌超氧化物歧化酶(SOD)和过氧化氢酶的32P标记DNA探针,通过Northern印迹分析评估抗氧化酶mRNA表达。在隐睾和对侧睾丸中,与对照睾丸相比,生殖细胞特异性的0.9 kb SOD和PHGPX mRNA转录水平显著降低(p < 0.05)。同样,在输出小管结扎后,与对照睾丸相比,0.9 kb SOD和PHGPX mRNA转录水平也降低(p < 0.05)。这些发现表明,输出小管结扎和隐睾症后睾丸mRNA转录水平的总体下降主要是由于生殖细胞耗竭。已有文献记载隐睾睾丸中抗氧化酶mRNA水平降低。进一步的实验可能会阐明与隐睾症中抗氧化剂减少相关的氧化应激增加的作用。氧化应激在与隐睾症相关的异常精子发生和肿瘤发生中是否起因果作用仍有待确定。