1-硝基芘和苯并[a]芘对人肺上皮A549细胞的联合细胞毒性  被引量:1

Combined effects of 1-nitropyrene and benzo(a)pyrene on cytotoxicity and DNA damage in human lung epithelial A549 cells

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作  者:尚羽[1] 周倩[1] 蒋玉婷[1] 

机构地区:[1]上海大学环境与化学工程学院环境污染与健康研究所,上海200444

出  处:《上海大学学报(自然科学版)》2016年第2期181-187,共7页Journal of Shanghai University:Natural Science Edition

基  金:国家自然科学基金资助项目(21107068;41561144007);上海大学长江学者和创新团队发展计划资助项目(IRT13078)

摘  要:1-硝基芘(1-nitropyrene,1-NP)是柴油车尾气中检测浓度最高的硝基多环芳烃.以1-NP为主体,人肺上皮A549细胞为研究对象,探讨了1-NP和苯并[a]芘(benzo(a)pyrene,B[a]p)的联合细胞毒性及其对DNA的损伤.联合染毒实验结果表明:当B[a]p和1-NP同时作用于A549细胞时,B[a]p能明显减弱由1-NP造成的细胞增殖抑制和细胞内活性氧簇(reactive oxygen species,ROS)水平升高,但对DNA的损伤与1-NP单独染毒组相近;利用B[a]p预染毒A549细胞24 h,能明显减弱由1-NP造成的细胞增殖抑制和ROS水平升高,但对DNA的损伤加剧.以上结果说明,1-NP和B[a]p联合作用可能是通过抑制ROS的生成来降低对细胞增殖的抑制,但所造成的对DNA损伤的加剧可能是通过其他的作用途径.Using human lung epithelial A549 cells, combined toxic effects of 1-nitropyrene (1-NP) and benzo(a)pyrene (B[a]p) were evaluated. The 1-NP caused a significantly concentration-dependent viability decrease, DNA damage and reactive oxygen species (ROS) generation. Compared with the groups treated with 1-NP alone, viability was significantly increased and ROS generation was significantly reduced in combined-treated groups with 1-NP and B[a]p. However, the DNA damage was significantly increased in the combined- treated groups compared with the groups treated with 1-NP alone. These results suggested that 1-NP may mediate the cytotoxic effects through ROS generation, and pretreatment, with B[a]p may inhibit ROS generation induced by 1-NP, and thereby reducing the cell death in A549 cells. However mechanisms of DNA damage deserves further investigations.

关 键 词:1-硝基芘 苯并[A]芘 大气颗粒物 DNA损伤 活性氧簇 

分 类 号:R994.6[医药卫生—毒理学]

 

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