Silva João P, Gomes Andreia C, Coutinho Olga P
CBMA - Molecular and Environmental Biology Centre/Biology Department, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
Eur J Pharmacol. 2008 Dec 28;601(1-3):50-60. doi: 10.1016/j.ejphar.2008.10.046. Epub 2008 Nov 5.
Biological systems are frequently exposed to excessive reactive oxygen species, causing a disturbance in the cells natural antioxidant defence systems and resulting in damage to all biomolecules, including nucleic acids. In fact, oxidative DNA damage is described as the type of damage most likely to occur in neuronal cells. In this study, three polyphenolic compounds, luteolin, quercetin and rosmarinic acid, were investigated for their protective effects against oxidative DNA damage induced in PC12 cells, a neuronal cell model. Although luteolin and quercetin prevented the formation of strand breaks to a greater extent than rosmarinic acid, this last one presented the highest capacity to repair strand breaks formation. In addition, rosmarinic acid was the only compound tested that increased the repair of oxidized nucleotidic bases induced with the photosensitizer compound [R]-1-[(10-chloro-4-oxo-3-phenyl-4H-benzo[a]quinolizin-1-yl) carbonyl]-2-pyrrolidine-methanol (Ro 19-8022). The activity of repair enzymes was indicated by the in vitro base excision repair assay, using a cell-free extract obtained from cells previously treated with the compounds to incise DNA. The protective effect of rosmarinic acid was further confirmed by the increased expression of OGG1 repair gene, observed through real time RT-PCR. The data obtained is indicative that rosmarinic acid seems to act on the intracellular mechanisms responsible for DNA repair, rather than by a direct effect on reactive oxygen species scavenging, as deducted from the effects observed for luteolin and quercetin. Therefore, these results suggest the importance of these polyphenols, and in particular rosmarinic acid, as protectors of oxidative stress-induced DNA damage that commonly occurs in several pathological conditions, such as neurodegenerative diseases.
生物系统经常暴露于过量的活性氧物种中,这会扰乱细胞的天然抗氧化防御系统,并导致包括核酸在内的所有生物分子受损。事实上,氧化DNA损伤被描述为最有可能在神经元细胞中发生的损伤类型。在本研究中,研究了三种多酚化合物,木犀草素、槲皮素和迷迭香酸,对神经细胞模型PC12细胞中诱导的氧化DNA损伤的保护作用。尽管木犀草素和槲皮素在防止链断裂形成方面比迷迭香酸更有效,但后者表现出修复链断裂形成的最高能力。此外,迷迭香酸是唯一测试的化合物,它能增加由光敏剂化合物[R]-1-[(10-氯-4-氧代-3-苯基-4H-苯并[a]喹嗪-1-基)羰基]-2-吡咯烷甲醇(Ro 19-8022)诱导的氧化核苷酸碱基的修复。通过使用从先前用这些化合物处理过的细胞中获得的无细胞提取物来切割DNA的体外碱基切除修复试验,表明了修复酶的活性。通过实时逆转录聚合酶链反应观察到OGG1修复基因表达的增加,进一步证实了迷迭香酸的保护作用。所获得的数据表明,迷迭香酸似乎作用于负责DNA修复的细胞内机制,而不是像从木犀草素和槲皮素观察到的效果推断的那样直接作用于活性氧清除。因此,这些结果表明这些多酚,特别是迷迭香酸,作为氧化应激诱导的DNA损伤的保护剂的重要性,这种损伤在几种病理状况下,如神经退行性疾病中经常发生。