Department of Oto-Rhino-Laryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University of Wuerzburg, Germany.
Toxicol Appl Pharmacol. 2010 Jun 1;245(2):219-25. doi: 10.1016/j.taap.2010.03.003. Epub 2010 Mar 7.
Cytotoxicity and genotoxicity of nitrogen dioxide (NO(2)) as part of urban exhaust pollution are widely discussed as potential hazards to human health. This study focuses on toxic effects of NO(2) in realistic environmental concentrations with respect to the current limit values in a human target tissue of volatile xenobiotics, the epithelium of the upper aerodigestive tract. Nasal epithelial cells of 10 patients were cultured as an air-liquid interface and exposed to 0.01 ppm NO(2), 0.1 ppm NO(2), 1 ppm NO(2), 10 ppm NO(2) and synthetic air for half an hour. After exposure, genotoxicity was evaluated by the alkaline single-cell microgel electrophoresis (Comet) assay and by induction of micronuclei in the micronucleus test. Depression of proliferation and cytotoxic effects were determined using the micronucleus assay and trypan blue exclusion assay, respectively. The experiments revealed genotoxic effects by DNA fragmentation starting at 0.01 ppm NO(2) in the Comet assay, but no micronucleus inductions, no changes in proliferation, no signs of necrosis or apoptosis in the micronucleus assay, nor did the trypan blue exclusion assay show any changes in viability. The present data reveal a possible genotoxicity of NO(2) in urban concentrations in a screening test. However, permanent DNA damage as indicated by the induction of micronuclei was not observed. Further research should elucidate the effects of prolonged exposure.
二氧化氮(NO2)作为城市废气污染的一部分,其细胞毒性和遗传毒性被广泛认为是对人类健康的潜在危害。本研究关注的是在当前挥发性外来物质的人体靶组织(上呼吸道的上皮)的限值内,NO2在实际环境浓度下的毒性作用。将 10 名患者的鼻腔上皮细胞培养为气液界面,并将其暴露于 0.01ppm、0.1ppm、1ppm、10ppm 的 NO2和合成空气中半小时。暴露后,通过碱性单细胞微凝胶电泳(彗星)试验和微核试验评估遗传毒性,通过微核试验诱导微核。通过微核试验和台盼蓝排斥试验分别测定增殖抑制和细胞毒性作用。实验结果显示,在彗星试验中,从 0.01ppm 的 NO2开始就出现了 DNA 片段化的遗传毒性效应,但没有微核诱导,微核试验中增殖没有变化,也没有出现坏死或凋亡的迹象,台盼蓝排斥试验也没有显示出活力的变化。本研究数据揭示了在城市浓度下,NO2可能具有遗传毒性,但未观察到微核诱导所表明的永久性 DNA 损伤。进一步的研究应该阐明长期暴露的影响。