Department of Biology, Faculty of Arts and Sciences, University of Çanakkale Onsekiz Mart, Terzioglu Campus, 17020 Çanakkale, Turkey.
Food Chem Toxicol. 2012 Oct;50(10):3475-9. doi: 10.1016/j.fct.2012.07.048. Epub 2012 Aug 2.
Oxidative DNA damage is an inescapable consequence for cells constantly exposed to oxidative stress derived from normal metabolic processes and from environmental factors. Phenolic compounds, which have strong antioxidant activity, prevent DNA damage by protecting the cells against harmful effects of oxidative stress. In this study, the effect of virgin olive oil phenolic extract (OOPE) was investigated on H2O2-induced mitochondrial DNA (mtDNA) and nuclear DNA (nDNA) damage in HeLa cells. DNA damage was assessed in mitochondria and two nuclear regions by using quantitative PCR (QPCR) assay. The cells were pre-treated with non-cytotoxic doses of OOPE for 4 h, and DNA damage was determined. OOPE alone does not change the steady-state level of DNA damage. The oxidative stress generated with 750 μM H2O2 caused two times greater damages in mtDNA compared to nDNA, which included the nonexpressed β-globin region (1.507±0.110 lesions/10 kb) and the expressed APEX1 gene (1.623±0.243 lesions/10 kb) with respect to the control region. When cells were preincubated with OOPE for 4 h, nDNA damage under stress condition was completely inhibited; however, mtDNA damage was not affected by this procedure. These results suggest that OOPE has a protective effect against nDNA damage in HeLa cells.
氧化 DNA 损伤是细胞不断暴露于源自正常代谢过程和环境因素的氧化应激下不可避免的后果。具有强抗氧化活性的酚类化合物通过保护细胞免受氧化应激的有害影响来防止 DNA 损伤。在这项研究中,研究了初榨橄榄油酚类提取物 (OOPE) 对 H2O2 诱导的 HeLa 细胞中线粒体 DNA (mtDNA) 和核 DNA (nDNA) 损伤的影响。通过定量 PCR (QPCR) 测定,在线粒体和两个核区评估了 DNA 损伤。用非细胞毒性剂量的 OOPE 预处理细胞 4 小时,然后测定 DNA 损伤。OOPE 本身不会改变 DNA 损伤的稳态水平。用 750 μM H2O2 产生的氧化应激导致 mtDNA 损伤比 nDNA 增加两倍,其中包括未表达的β-珠蛋白区域(1.507±0.110 个损伤/10 kb)和表达的 APEX1 基因(1.623±0.243 个损伤/10 kb)与对照区相比。当细胞用 OOPE 预孵育 4 小时时,应激条件下的 nDNA 损伤完全被抑制;然而,mtDNA 损伤不受此过程的影响。这些结果表明,OOPE 对 HeLa 细胞中的 nDNA 损伤具有保护作用。