RRC ID 43718
Author Kato T, Totsuka Y, Ishino K, Matsumoto Y, Tada Y, Nakae D, Goto S, Masuda S, Ogo S, Kawanishi M, Yagi T, Matsuda T, Watanabe M, Wakabayashi K.
Title Genotoxicity of multi-walled carbon nanotubes in both in vitro and in vivo assay systems.
Journal Nanotoxicology
Abstract The genotoxic effects of multi-walled carbon nanotubes (MWCNTs) were examined by using in vitro and in vivo assays. MWCNTs significantly induced micronuclei in A549 cells and enhanced the frequency of sister chromatid exchange (SCE) in CHO AA8 cells. When ICR mice were intratracheally instilled with a single dose (0.05 or 0.2 mg/animal) of MWCNTs, DNA damage of the lungs, analysed by comet assay, increased in a dose-dependent manner. Moreover, DNA oxidative damage, indicated by 8-oxo-7,8-dihydro-2'-deoxyguanosine and heptanone etheno-deoxyribonucleosides, occurred in the lungs of MWCNT-exposed mice. The gpt mutation frequencies significantly increased in the lungs of MWCNT-treated gpt delta transgenic mice. Transversions were predominant, and G:C to C:G was clearly increased by MWCNTs. Moreover, many regions immunohistochemically stained for inducible NO synthase and nitrotyrosine were observed in the lungs of MWCNT-exposed mice. Overall, MWCNTs were shown to be genotoxic both in in vitro and in vivo tests; the mechanisms probably involve oxidative stress and inflammatory responses.
Volume 7(4)
Pages 452-61
Published 2013-6-1
DOI 10.3109/17435390.2012.674571
PMID 22397533
MeSH Animals CHO Cells Cricetinae Cricetulus DNA Adducts Dose-Response Relationship, Drug Lipid Peroxidation Lung / drug effects Lung / pathology Male Mice Mice, Inbred ICR Micronucleus Tests Mutation / drug effects Nanotubes, Carbon / chemistry Nanotubes, Carbon / toxicity* Oxidation-Reduction Sister Chromatid Exchange / drug effects
IF 4.925
Times Cited 63
WOS Category TOXICOLOGY NANOSCIENCE & NANOTECHNOLOGY
Resource
Human and Animal Cells A549