首页> 外文期刊>Archivum immunologiae et therapiae experimentalis >Increased salivary level of 8-hydroxydeoxyguanosine is a marker of premature oxidative mitochondrial DNA damage in gingival tissue of patients with periodontitis.
【24h】

Increased salivary level of 8-hydroxydeoxyguanosine is a marker of premature oxidative mitochondrial DNA damage in gingival tissue of patients with periodontitis.

机译:唾液中8-羟基脱氧鸟苷水平的升高是牙周炎患者牙龈组织中过早氧化线粒体DNA损伤的标志。

获取原文
获取原文并翻译 | 示例
           

摘要

INTRODUCTION: Oxidative stress may contribute to the pathogenesis of periodontitis. However, the detailed molecular mechanism remains unclear. Both 8-hydroxydeoxyguanosine (8-OHdG) and mitochondrial DNA (mtDNA) deletion have been reported as early oxidative DNA damage markers. In this study, 8-OHdG levels in saliva and mtDNA deletions in gingival tissue of patients with chronic periodontitis (CP) were evaluated. MATERIALS AND METHODS: Gingival tissue and whole saliva samples were collected from 32 patients with CP and 32 healthy control subjects. To determine the clinical condition of each subject, the plaque index, gingival index, clinical attachment level (CAL), and probing depth (PD) were measured. Using the ELISA and polymerase chain reaction methods, the salivary 8-OHdG levels and the 7.4-kbp and 5-kbp mtDNA deletions were examined. RESULTS: The 5-kbp mtDNA deletion was detected in 20 of the 32 periodontitis patients (62.5%), but was not detected in the healthy controls. The mean value of 8-OHdG in the saliva of the periodontitis patients with deleted mtDNA was significantly higher than in the patients with non-deleted mtDNA (p<0.01). Also, significant correlation was found between the occurrence of the 5-kbp mtDNA deletion and salivary 8-OHdG levels (p<0.01). Similar correlations were detected between salivary 8-OHdG levels and age, PD, and CAL (p<0.01, p<0.05). CONCLUSION: Increased oxidative stress may lead to premature oxidative DNA damage in the gingival tissue of periodontitis patients and the salivary 8-OHdG level may signify premature oxidative mtDNA damage in diseased gingival tissue.
机译:简介:氧化应激可能导致牙周炎的发病机理。但是,详细的分子机制仍不清楚。 8羟基脱氧鸟苷(8-OHdG)和线粒体DNA(mtDNA)删除已被报道为早期氧化DNA损伤标记。在这项研究中,评估了慢性牙周炎(CP)患者唾液中的8-OHdG水平和牙龈组织中的mtDNA缺失。材料与方法:从32例CP患者和32例健康对照受试者中收集牙龈组织和整个唾液样本。为了确定每个受试者的临床状况,测量了斑块指数,牙龈指数,临床附着水平(CAL)和探测深度(PD)。使用ELISA和聚合酶链反应方法,检测唾液中的8-OHdG水平以及7.4-kbp和5-kbp mtDNA缺失。结果:32例牙周炎患者中有20例(62.5%)检测到5-kbp mtDNA缺失,但在健康对照组中未检测到。缺失mtDNA的牙周炎患者唾液中8-OHdG的平均值显着高于未缺失mtDNA的患者(p <0.01)。同样,在5-kbp mtDNA缺失的发生与唾液中的8-OHdG水平之间也发现了显着相关性(p <0.01)。唾液中的8-OHdG水平与年龄,PD和CAL之间也发现了相似的相关性(p <0.01,p <0.05)。结论:增加的氧化应激可能导致牙周炎患者牙龈组织中的过早氧化性DNA损伤,唾液中的8-OHdG水平可能表明患病的牙龈组织中的过早氧化性mtDNA损伤。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号