Suzuki Tetsuya, Miura Nobuhiko, Hojo Rieko, Yanagiba Yukie, Suda Megumi, Hasegawa Tatsuya, Miyagawa Muneyuki, Wang Rui-Sheng
1Division of Industrial Toxicology and Health Effects Research, National Institute of Occupational Safety and Health, 6-21-1 Nagao, Tama-ku, Kawasaki, Kanagawa 214-8585 Japan.
2Present address: Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553 Japan.
Genes Environ. 2020 Feb 10;42:7. doi: 10.1186/s41021-020-0146-3. eCollection 2020.
A variety of in vivo and in vitro studies to assess the genotoxicity of titanium dioxide nanoparticles (TiO NPs) have been reported, but the results are inconsistent. Recently, we reported that TiO NPs exhibit no genotoxic effects in the liver and erythrocytes during a relatively brief period following intravenous injection into mice. However, there is no information about long-term genotoxicity due to TiO NP accumulation in tissues. In this study, we investigated the long-term mutagenic effects of TiO NPs and the localization of residual TiO NPs in mouse liver after multiple intravenous injections.
Male delta C57BL/6 J mice were administered with various doses of TiO NPs weekly for 4 consecutive weeks. The long-term mutagenic effects on the liver were analyzed using and Spi mutation assays 90 days after the final injection. We also quantified the amount of titanium in the liver using inductively coupled plasma mass spectrometry and observed the localization of TiO NPs in the liver using transmission electron microscopy. Although TiO NPs were found in the liver cells, the and Spi mutation frequencies in the liver were not significantly increased by the TiO NP administration.
These results clearly show that TiO NPs have no mutagenic effects on the liver, even though the particles remain in the liver long-term.
已有多项体内和体外研究评估二氧化钛纳米颗粒(TiO NPs)的遗传毒性,但结果并不一致。最近,我们报道静脉注射到小鼠体内后,在相对较短的时间内,TiO NPs在肝脏和红细胞中未表现出遗传毒性作用。然而,关于由于TiO NPs在组织中积累导致的长期遗传毒性尚无相关信息。在本研究中,我们调查了多次静脉注射后TiO NPs的长期诱变作用以及残留TiO NPs在小鼠肝脏中的定位。
雄性δC57BL/6 J小鼠连续4周每周给予不同剂量的TiO NPs。在最后一次注射90天后,使用 和Spi突变试验分析对肝脏的长期诱变作用。我们还使用电感耦合等离子体质谱法对肝脏中的钛含量进行了定量,并使用透射电子显微镜观察了TiO NPs在肝脏中的定位。尽管在肝细胞中发现了TiO NPs,但给予TiO NPs后肝脏中的 和Spi突变频率并未显著增加。
这些结果清楚地表明,即使TiO NPs长期留存于肝脏中,它们对肝脏也没有诱变作用。