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Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice

BACKGOUND: A variety of in vivo and in vitro studies to assess the genotoxicity of titanium dioxide nanoparticles (TiO(2) NPs) have been reported, but the results are inconsistent. Recently, we reported that TiO(2) NPs exhibit no genotoxic effects in the liver and erythrocytes during a relatively br...

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Autores principales: Suzuki, Tetsuya, Miura, Nobuhiko, Hojo, Rieko, Yanagiba, Yukie, Suda, Megumi, Hasegawa, Tatsuya, Miyagawa, Muneyuki, Wang, Rui-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011542/
https://www.ncbi.nlm.nih.gov/pubmed/32071618
http://dx.doi.org/10.1186/s41021-020-0146-3
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author Suzuki, Tetsuya
Miura, Nobuhiko
Hojo, Rieko
Yanagiba, Yukie
Suda, Megumi
Hasegawa, Tatsuya
Miyagawa, Muneyuki
Wang, Rui-Sheng
author_facet Suzuki, Tetsuya
Miura, Nobuhiko
Hojo, Rieko
Yanagiba, Yukie
Suda, Megumi
Hasegawa, Tatsuya
Miyagawa, Muneyuki
Wang, Rui-Sheng
author_sort Suzuki, Tetsuya
collection PubMed
description BACKGOUND: A variety of in vivo and in vitro studies to assess the genotoxicity of titanium dioxide nanoparticles (TiO(2) NPs) have been reported, but the results are inconsistent. Recently, we reported that TiO(2) 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(2) NP accumulation in tissues. In this study, we investigated the long-term mutagenic effects of TiO(2) NPs and the localization of residual TiO(2) NPs in mouse liver after multiple intravenous injections. RESULTS: Male gpt delta C57BL/6 J mice were administered with various doses of TiO(2) NPs weekly for 4 consecutive weeks. The long-term mutagenic effects on the liver were analyzed using gpt 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(2) NPs in the liver using transmission electron microscopy. Although TiO(2) NPs were found in the liver cells, the gpt and Spi(−) mutation frequencies in the liver were not significantly increased by the TiO(2) NP administration. CONCLUSIONS: These results clearly show that TiO(2) NPs have no mutagenic effects on the liver, even though the particles remain in the liver long-term.
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spelling pubmed-70115422020-02-18 Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice Suzuki, Tetsuya Miura, Nobuhiko Hojo, Rieko Yanagiba, Yukie Suda, Megumi Hasegawa, Tatsuya Miyagawa, Muneyuki Wang, Rui-Sheng Genes Environ Research BACKGOUND: A variety of in vivo and in vitro studies to assess the genotoxicity of titanium dioxide nanoparticles (TiO(2) NPs) have been reported, but the results are inconsistent. Recently, we reported that TiO(2) 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(2) NP accumulation in tissues. In this study, we investigated the long-term mutagenic effects of TiO(2) NPs and the localization of residual TiO(2) NPs in mouse liver after multiple intravenous injections. RESULTS: Male gpt delta C57BL/6 J mice were administered with various doses of TiO(2) NPs weekly for 4 consecutive weeks. The long-term mutagenic effects on the liver were analyzed using gpt 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(2) NPs in the liver using transmission electron microscopy. Although TiO(2) NPs were found in the liver cells, the gpt and Spi(−) mutation frequencies in the liver were not significantly increased by the TiO(2) NP administration. CONCLUSIONS: These results clearly show that TiO(2) NPs have no mutagenic effects on the liver, even though the particles remain in the liver long-term. BioMed Central 2020-02-10 /pmc/articles/PMC7011542/ /pubmed/32071618 http://dx.doi.org/10.1186/s41021-020-0146-3 Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Suzuki, Tetsuya
Miura, Nobuhiko
Hojo, Rieko
Yanagiba, Yukie
Suda, Megumi
Hasegawa, Tatsuya
Miyagawa, Muneyuki
Wang, Rui-Sheng
Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
title Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
title_full Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
title_fullStr Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
title_full_unstemmed Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
title_short Genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
title_sort genotoxicity assessment of titanium dioxide nanoparticle accumulation of 90 days in the liver of gpt delta transgenic mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011542/
https://www.ncbi.nlm.nih.gov/pubmed/32071618
http://dx.doi.org/10.1186/s41021-020-0146-3
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