期刊文献+

多壁碳纳米管致A549细胞毒性与氧化损伤的研究 被引量:3

In vitro cytotoxicity and oxidative damage effects of Multi-wall carbon nanotube on A549 cell
下载PDF
导出
摘要 目的探讨多壁碳纳米管(MWCNTs)对人Ⅱ型肺泡上皮细胞(AT-Ⅱ)A549细胞的体外细胞毒性和氧化损伤作用。方法用脱氧核糖核酸钠盐(deoxyribonucleic acid sodium salt,DNA钠盐)提高MWCNTs的分散度,设4个浓度组(2.5、10、25和100μg/ml)、DNA钠盐溶剂对照组和生理盐水对照组,染毒24h后,用MTT法观察细胞毒性,并根据染毒后总蛋白(TP)、乳酸脱氢酶(LDH)、一氧化氮(NO)、谷胱甘肽(GSH)、超氧化物歧化酶(SOD)和丙二醛(MDA)的变化情况分析MWCNTs的细胞毒性和氧化损伤作用。结果25、100μg/ml浓度组细胞存活率及细胞毒性和氧化损伤指标均有不同程度的改变,呈一定的暴露-反应关系;随着染毒剂量的升高,细胞和其上清液中TP、LDH、NO和MDA含量随之升高,而GSH和SOD含量随之降低,且呈一定的暴露-反应关系;且与细胞发生融解破碎,间隙加大等形态学改变情况相符。结论MWCNTs对A549细胞产生一定的毒性和氧化损伤作用,且随剂量的增大而增强。 Objective To study the in vitro cytotoxicity and oxidative damage effects of Multi-wall Carbon Nanotube on A549 cells. Methods The A549 cells were treated with different concentrations of MWCNTs (2.5,10,25,100μg/ml), slovent control and saline control for 24 h. MTr assays were applied for testing A549 cell activity in vitro, total protein (TP), lactate dehydrogenase( LDH), nitrogen monoxidum (NO), glutathione ( GSH ), superoxide dismutase ( SOD), and malondialdehyde (MDA) in supernate and intra-cellular were determined to evaluate the in vitro cytotoxicity and oxidative damage effects of NWCNTs on A459 cells. The morphology changes of A549 cells were also observed. Results In comparison with control, the viabilities of A549 cells were decreased significantly after exposure to MWCNTs. The level of TP,LDH ,NO and MDA in exposed groups were higher, while GSH and SOD level were lower than control with a significant dose-effect relationship, which accord to the morphology changs of A549 cells exposed to MWCNTs. Conclusion MWCNTs induces cytotoxity and oxidative stress on A549 cells. With the increases of the concentration of MWCNTs.
出处 《毒理学杂志》 CAS CSCD 北大核心 2008年第2期92-95,共4页 Journal of Toxicology
基金 上海市科学技术委员会国际合作项目(05520708)
关键词 双壁碳纳米 细胞毒性 氧化损伤 Multi-wall carbon nanotubes Cytotoxicity Oxidative stress
  • 相关文献

参考文献11

  • 1Iijima S. Helical microtubules of graphitic carbon. Nature, 1991,354 : 56-58.
  • 2Ebbesen TW, Lezec H J, Hiura H, et al. Electrical conductivity of individual carbon nanotubos. Nature, 1996,49 : 26-32.
  • 3Oberd~rster G, Ferin J, Lehnert BE. Correlation between particle size, in vivo particle persistence and lung injury. Environ Health Perspect, 1994, 102:173-179.
  • 4Shvedova AA, Castranova V, Kisin ER, et al. Exposure to carbon nanotube material: assessment of nanotube cytotoxicity using human keratinocyte cells. J Toxicol Environ Health A, 2003,66 : 1909-1926.
  • 5Calcabrini A, Meschini S, Marra M, et al. Fine environmental particulate engenders alterations in human lung epithelial A549 cells. Environ Res,2004, 95 : 82-91.
  • 6Nel A, Xia T, Madler L, et al. Toxic potential of materials at the nanolevel. Science, 2006,311 : 622-627.
  • 7Monteiro-Riviere NA, Nemanich RJ, lnman AO, et al. Multiwalled carbon nanotube interactions with human epidermal keratinocytes. Nano Lett, 2005,5 : 2448-2464.
  • 8Ding L, Stilwell J, Zhang T, et al. Molecular characterization of the cytotoxic mechanism of muhiwall carbon nanotubes and nano-onions on human skin fibroblast. Toxicol Lett, 2005,155 : 377-384.
  • 9Brune B, Zhou J, Von Knethen A. Nitric oxide oxidative stress and apoptosis. Kidney lnt Suppl, 2003,84:22-27.
  • 10袁勤生.超氧化物歧化酶的研究现状及应用前景[J].中国药学杂志,1991,26(8):456-459. 被引量:37

共引文献36

同被引文献38

  • 1贾光,郑玉新.充分认识纳米材料安全性研究的重要意义[J].中华预防医学杂志,2007,41(2):83-84. 被引量:10
  • 2邹小农.中国肺癌流行病学[J].中华肿瘤防治杂志,2007,14(12):881-883. 被引量:151
  • 3Takenaka S, Karg E, Roth C, et al. Pulmonary and systemic distribution of inhaled tdtrafine silver particles in rats. Environ Health Pempect, 2001, 109(S4) : 547 -551.
  • 4Oberdorster G, Ferin J, Lehnert BE. Correlation between particle size, in vivo particle persistence, and lung injury . Environ Health Perspect, 1994, 102 Suppl 5:173 -179.
  • 5Ferin J, Oberdorster G, Penney DP. Pulmonary retention oi uhrafine and fine particles in rats. Am J Reapir Cell Mol Biol, 1992, 6(5) : 535 -542.
  • 6Renwick LC, Brown D, Clouter A, et al. Increased inflammation and altered macrophage chemotactic responses caused by two uhrafine particle types. Occup Environ Med, 2004, 61 : 442 - 447.
  • 7Lain C W, James J, Tmccluskey R, et al. Pulmonary toxicity of single-wall carbon nanotubes in mice 7 and 90 days after intratracheal instillation. Toxicol Sci, 2004, 77 : 126 - 134.
  • 8Renwick L C, Brow N D, Clouter A, et al. Increased inflammation and altered macrophage chemotactic response caused by two ultrafine particle types. Occup Environ Med, 2004, 61, 442-447.
  • 9Edirto B, James BM, Brian AW, et al. Pulmonary responses of mice, rats and hamsters to subchronicnltion of ultrafine titanium dioxide particles. Toxicol Sei, 2004, 77 : 34 7 - 357.
  • 10Tan M H, Commens CA, Burnett L, et al. A pilot study on the percutaneous absorption of mlcrofine titanium dioxide from sunsereens. Aus J Dermatol, 1996, 37(4) : 185 - 187.

引证文献3

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部