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大鼠附睾中抗氧化酶mRNA的鉴定与特性分析

Identification and characterization of antioxidant enzyme mRNAs in the rat epididymis.

作者信息

Zini A, Schlegel P N

机构信息

James Buchanan Brady Foundation, Department of Urology, New York, USA.

出版信息

Int J Androl. 1997 Apr;20(2):86-91. doi: 10.1046/j.1365-2605.1997.00039.x.

Abstract

Spermatozoa are highly sensitive to oxidative stress. The epididymis, a natural sperm reservoir, has maturational and storage functions. The epididymis may also protect spermatozoa from oxidative injury by elaborating scavengers of reactive oxygen species (ROS). Therefore, we have evaluated the mRNA expression of antioxidant enzymes in the normal rat epididymis and the effects of efferent duct ligation no the expression of these enzymes. Adult rat epididymides were harvested, divided into caput, corpus and cauda and processed for RNA extraction. Additional adult rats were subjected to unilateral efferent duct ligation and the epididymides harvested at 1, 4, 8, 16 or 28 days after the procedure. Antioxidant enzyme mRNA expression was assessed by Northern blot analysis using 32P-labelled DNA probes derived from known cDNA sequences for classical cellular glutathione peroxidase (GSHPx), phospholipid hydroperoxide glutathione peroxidase (PHGPX), secretory epididymal glutathione peroxidase (E-GPX), copper-zinc superoxide dismutase (SOD), secretory epididymal superoxide dismutase (E-SOD) and catalase. Specific mRNA levels were measured, with gene expression evaluated relative to total RNA, not per organ. Variations in lane loading were controlled by measuring the levels of 28S ribosomal RNA. GSHPx, PHGPX, SOD and catalase mRNA were detected in the caput, corpus and cauda epididymis. E-GPX mRNA was only detected in the caput, whereas E-SOD mRNA was primarily detected in the corpus. At 28 days after efferent duct ligation, epididymal weight decreased by 34% relative to controls (p < 0.05). With the exception of PHGPX, the relative mRNA levels of the antioxidant enzymes studied did not change after efferent duct ligation. This study demonstrates that mRNAs for multiple antioxidant enzymes are expressed in the epididymis and that the relative expression of these enzymes remains largely unchanged in response to efferent duct ligation. Taken together, these results suggest that antioxidant enzymes may play an important, region-specific role in epididymal function. Expression of the secretory antioxidant enzymes E-SOD and E-GPX is region-specific, indicating that the need for antioxidant enzymes may vary along the length of the epididymis.

摘要

精子对氧化应激高度敏感。附睾作为天然的精子储存库,具有成熟和储存功能。附睾还可能通过产生活性氧(ROS)清除剂来保护精子免受氧化损伤。因此,我们评估了正常大鼠附睾中抗氧化酶的mRNA表达以及输出小管结扎对这些酶表达的影响。采集成年大鼠的附睾,分为头段、体段和尾段,进行RNA提取。另外的成年大鼠进行单侧输出小管结扎,并在手术后1、4、8、16或28天采集附睾。使用源自已知cDNA序列的32P标记DNA探针,通过Northern印迹分析评估抗氧化酶mRNA的表达,这些探针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)、分泌型附睾谷胱甘肽过氧化物酶(E-GPX)、铜锌超氧化物歧化酶(SOD)、分泌型附睾超氧化物歧化酶(E-SOD)和过氧化氢酶。测量特定mRNA水平,基因表达相对于总RNA进行评估,而非每个器官。通过测量28S核糖体RNA水平来控制泳道上样量的变化。在附睾头段、体段和尾段均检测到GSHPx、PHGPX、SOD和过氧化氢酶的mRNA。E-GPX mRNA仅在附睾头段检测到,而E-SOD mRNA主要在附睾体段检测到。输出小管结扎后28天,附睾重量相对于对照组下降了34%(p < 0.05)。除PHGPX外,所研究的抗氧化酶的相对mRNA水平在输出小管结扎后未发生变化。本研究表明,多种抗氧化酶的mRNA在附睾中表达,并且这些酶的相对表达在输出小管结扎后基本保持不变。综上所述,这些结果表明抗氧化酶可能在附睾功能中发挥重要的区域特异性作用。分泌型抗氧化酶E-SOD和E-GPX的表达具有区域特异性,表明沿附睾长度对抗氧化酶的需求可能有所不同。

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