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尿石症中锰超氧化物歧化酶(Mn-SOD)基因多态性

Manganese superoxide dismutase (Mn-SOD) gene polymorphisms in urolithiasis.

作者信息

Tugcu Volkan, Ozbek Emin, Aras Bekir, Arisan Serdar, Caskurlu Turhan, Tasci Ali Ihsan

机构信息

1st Urology Clinics, Bakirköy Research and Training Hospital, Gul D-5 Blok D:35, 34538 Bahçesehir/Istanbul, Turkey.

出版信息

Urol Res. 2007 Oct;35(5):219-24. doi: 10.1007/s00240-007-0103-7. Epub 2007 Jul 13.

Abstract

Polymorphism in manganese superoxide dismutase gene (Mn-SOD) is a new approach to identify its probable association with urolithiasis. Oxidative stress may be involved in the development of stone formation in the renal system. MnSOD is one of the primary enzymes that directly scavenges potential harmful oxidizing species. A valine (Val) to alanine (Ala) substitution at amino acid 16, occurring in the mitochondrial targeting sequence of the MnSOD gene, has been associated with an increase in urolithiasis risk. This study was conducted to investigate the association of MnSOD gene polymorphism with the risk of urolithiasis. We investigated the MnSOD in 66 stone-forming adults and 72 healthy volunteers. DNA was isolated from peripheral blood and genotyping was performed with PCR-based methods. Then PCR products were cut by BsaW1. Products were run on 3% agarose gel, 246 bp regions were 1-Ala-9, 164 and 82 bp products were determined as 2 Val-9. Chi-square test was used for comparison between patients and controls. In the control group the homozygote Ala allele was significantly higher than in the patient group (P < 0.01). The distribution of Ala/Val and homozygote Val alleles in the patient group was significantly higher than in the control group (P < 0.05). MnSOD genotype determination may provide a tool to identify individuals who are at risk of urolithiasis. This experiment also provides data about antioxidant status and stone formation.

摘要

锰超氧化物歧化酶基因(Mn-SOD)多态性是确定其与尿石症可能关联的一种新方法。氧化应激可能参与了泌尿系统结石形成的过程。MnSOD是直接清除潜在有害氧化物质的主要酶之一。MnSOD基因线粒体靶向序列中第16位氨基酸由缬氨酸(Val)替换为丙氨酸(Ala),与尿石症风险增加有关。本研究旨在探讨MnSOD基因多态性与尿石症风险的关联。我们对66名结石形成的成年人和72名健康志愿者进行了MnSOD检测。从外周血中分离DNA,并采用基于PCR的方法进行基因分型。然后用BsaW1切割PCR产物。产物在3%琼脂糖凝胶上电泳,246 bp区域为1-Ala-9,164和82 bp产物被确定为2 Val-9。采用卡方检验对患者和对照组进行比较。对照组中纯合子Ala等位基因显著高于患者组(P < 0.01)。患者组中Ala/Val和纯合子Val等位基因的分布显著高于对照组(P < 0.05)。MnSOD基因型测定可能为识别有尿石症风险的个体提供一种工具。本实验还提供了有关抗氧化状态和结石形成的数据。

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