首页> 外文期刊>International journal of high dilution research >Hydrated Fullerene C60 Decreases Oxidative Damage of Human Bronchial Epithelium Cells DNA
【24h】

Hydrated Fullerene C60 Decreases Oxidative Damage of Human Bronchial Epithelium Cells DNA

机译:水合富勒烯C60降低人支气管上皮细胞DNA的氧化损伤

获取原文
       

摘要

Background: Hydrated Fullerene C60 is a 60 carbon atoms symmetrical molecule that can be foundin nature. Being transferred into aqueous solution, a hydrophobic C60 establishes HydratedFullerene C60 (HyFnC60) water solutions that possess oxidation balancing properties in a wide rangeof concentrations (2.5×10-6 – 2.5×10-19 М). Nano-particles of silica (SiO). Nano-particles of silica (SiO2) can initiate reactive oxygenspecies (ROS) production in aqueous solutions. As silica is a common pollutant and a component ofmanufactured goods, one of the most probable ways of its penetration into human body isinhalation followed by an increased risk of chronic inflammation and cell degeneration due to ROSproduction inside the cells and in the extracellular space.Aims: In this study we focused on the possibility of DNA protection of human bronchial epithelialcells (HBEpCs) of oxidative damage by silica nanoparticles with HyFnC60 in a wide range ofconcentrations.Methodology: Cultivated cells were treated with 50 mg/ml nano-sized SiO2. HBEpCs DNA strandbreaks were accessed by comet assay. Intracellular ROS production was measured by DCFH–DAfluorescent spectrophotometry. HyFnC60 were added to the cell culture medium before treatmentwith silica. The calculated concentrations of HyFnC60 in the medium were 1×10-7 М). Nano-particles of silica (SiO 1×10-11 М). Nano-particles of silica (SiO,1×10-14 М). Nano-particles of silica (SiO and 1×10-17 М). Nano-particles of silica (SiO. The solutions of HyFnC60 were prepared by 10- and 100-fold serialdilutions of HyFnC60 stock solution in pure water. Results were evaluated statistically by Student`st-test and variance analysis by Statistica? software.Results and discussion: We have found that in case of pre-treatment of cells with 1×10-7 М). Nano-particles of silica (SiO and1×10-17 М). Nano-particles of silica (SiO HyFnC60 prior addition of silica DNA damage was decreased. According to DCFH–DAfluorescent microscopy a significant decrease of ROS was observed in case of addition of HyFnC60 tothe concentration of 1×10-7 М). Nano-particles of silica (SiO only. In case of simultaneous treatment of cells with silica andHyFnC60 cell damage was decreased at HyFnC60 concentration of 1×10-17 М). Nano-particles of silica (SiO. This data proves thatDNA was damaged by ROS induced by silica nanoparticles. Moreover, the data confirm thatHyFnC60 works as regulator of redox and free radical processes at low concentrations.
机译:背景:水合富勒烯C60是60个碳原子对称的分子,可以在自然界中发现。疏水性C60被转移到水溶液中,形成HydratedFullerene C60(HyFnC60)水溶液,该溶液在很宽的浓度范围内(2.5×10-6 – 2.5×10-19М)具有氧化平衡特性。二氧化硅(SiO)的纳米粒子。二氧化硅(SiO2)的纳米颗粒可以引发水溶液中活性氧(ROS)的产生。由于二氧化硅是一种常见的污染物,是制成品的组成部分,因此最可能的渗透途径之一是吸入到人体中,即吸入,然后由于细胞内和细胞外空间产生ROS而导致慢性炎症和细胞变性的风险增加。在这项研究中,我们重点研究了在多种浓度下用HyFnC60对二氧化硅纳米颗粒的氧化损伤对人支气管上皮细胞(HBEpCs)的DNA保护的可能性。方法:用50 mg / ml纳米SiO2处理培养的细胞。 HBEpCs DNA链断裂通过彗星分析获得。用DCFH-DA荧光分光光度法测量细胞内ROS的产生。在用二氧化硅处理之前,将HyFnC60添加到细胞培养基中。培养基中HyFnC60的计算浓度为1×10-7М)。二氧化硅的纳米颗粒(SiO 1×10-11М)。二氧化硅的纳米粒子(SiO,1×10-14М)。二氧化硅的纳米粒子(SiO和1×10-17М)。通过在纯水中分别对HyFnC60储液进行10倍和100倍系列稀释来制备纳米二氧化硅(SiO。HyFnC60溶液),并通过Studentst检验对统计结果进行评估,并使用Statistica?软件进行方差分析。讨论:我们发现在用1×10-7М预处理细胞的情况下。二氧化硅的纳米颗粒(SiO和1×10-17М)。二氧化硅的纳米颗粒(加入二氧化硅DNA之前的SiO HyFnC60减少了。根据DCFH-DA荧光显微镜观察,如果将HyFnC60添加到1×10-7М的浓度,则ROS显着降低)。二氧化硅的纳米颗粒(仅SiO。在同时用二氧化硅和HyFnC60处理细胞的情况下,当HyFnC60浓度为1×10-17М时,细胞损伤会减少)。二氧化硅(SiO。)纳米颗粒。该数据证明DNA被二氧化硅纳米颗粒诱导的ROS破坏。此外,该数据证实HyFnC60在低浓度下可作为氧化还原和自由基过程的调节剂。

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