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Model combustion-generated particulate matter containing persistent free radicals redox cycle to produce reactive oxygen species

机译:对包含持久性自由基氧化还原循环的燃烧产生的颗粒物质进行建模,以产生活性氧

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摘要

Particulate matter (PM) is emitted during thermal decomposition of waste. During this process, aromatic compounds chemisorb to the surface of metal-oxide-containing PM, forming a surface-stabilized environmentally persistent free radical (EPFR). We hypothesized that EPFR-containing PM redox cycle to produce ROS and that this redox cycle is maintained in biological environments. To test our hypothesis, we incubated model EPFRs with the fluorescent probe dihydrorhodamine (DHR). Marked increases in DHR fluorescence were observed. Using a more specific assay, hydroxyl radicals ( ?OH) were also detected, and their level was further increased by cotreatment with thiols or ascorbic acid (AA), known components of epithelial lining fluid. Next, we incubated our model EPFR in bronchoalveolar lavage fluid (BALF) or serum. Detection of EPFRs and ?OH verified that PM generate ROS in biological fluids. Moreover, incubation of pulmonary epithelial cells with EPFR-containing PM increased ?OH levels compared to those in PM lacking EPFRs. Finally, measurements of oxidant injury in neonatal rats exposed to EPFRs by inhalation suggested that EPFRs induce an oxidant injury within the lung lining fluid and that the lung responds by increasing antioxidant levels. In summary, our EPFR-containing PM redox cycle to produce ROS, and these ROS are maintained in biological fluids and environments. Moreover, these ROS may modulate toxic responses of PM in biological tissues such as the lung.
机译:废物热分解过程中会排放出颗粒物(PM)。在此过程中,芳香族化合物化学吸附到含金属氧化物的PM表面,形成表面稳定的环境持久性自由基(EPFR)。我们假设含EPFR的PM氧化还原循环产生ROS,并且该氧化还原循环在生物环境中得以维持。为了检验我们的假设,我们将模型EPFR与荧光探针二氢罗丹明(DHR)孵育。观察到DHR荧光明显增加。使用更具体的分析方法,还可以检测到羟基自由基(?OH),并通过与硫醇或抗坏血酸(AA)(上皮内衬液的已知成分)共同处理进一步提高了羟基自由基的水平。接下来,我们将模型EPFR在支气管肺泡灌洗液(BALF)或血清中孵育。对EPFR和OH的检测证实了PM在生物流体中产生ROS。此外,与缺乏EPFR的PM相比,用含EPFR的PM孵育肺上皮细胞可增加ΔOH水平。最后,对通过吸入暴露于EPFR的新生大鼠的氧化损伤的测量结果表明,EPFR在肺内衬液中引起氧化损伤,并且肺通过增加抗氧化剂水平做出反应。总之,我们的含EPFR的PM氧化还原循环会产生ROS,并且这些ROS保持在生物体液和环境中。此外,这些ROS可能会调节生物组织(如肺)中PM的毒性反应。

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