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Acute toxicity and genotoxicity of silver nanoparticle in rats
OBJECTIVE: The potential risk of a nanoparticle as a medical application has raised wide concerns, and this study aims to investigate silver nanoparticle (AgNP)-induced acute toxicities, genotoxicities, target organs and the underlying mechanisms. METHODS: Sprague-Dawley rats were randomly divided i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617228/ https://www.ncbi.nlm.nih.gov/pubmed/28953974 http://dx.doi.org/10.1371/journal.pone.0185554 |
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author | Wen, Hairuo Dan, Mo Yang, Ying Lyu, Jianjun Shao, Anliang Cheng, Xiang Chen, Liang Xu, Liming |
author_facet | Wen, Hairuo Dan, Mo Yang, Ying Lyu, Jianjun Shao, Anliang Cheng, Xiang Chen, Liang Xu, Liming |
author_sort | Wen, Hairuo |
collection | PubMed |
description | OBJECTIVE: The potential risk of a nanoparticle as a medical application has raised wide concerns, and this study aims to investigate silver nanoparticle (AgNP)-induced acute toxicities, genotoxicities, target organs and the underlying mechanisms. METHODS: Sprague-Dawley rats were randomly divided into 4 groups (n = 4 each group), and AgNP (containing Ag nanoparticles and released Ag(+), 5 mg/kg), Ag(+) (released from the same dose of AgNP, 0.0003 mg/kg), 5% sucrose solution (vechicle control) and cyclophophamide (positive control, 40 mg/kg) were administrated intravenously for 24 h respectively. Clinical signs and body weight of rats were recorded, and the tissues were subsequently collected for biochemical examination, Ag(+) distribution detection, histopathological examination and genotoxicity assays. RESULTS: The rank of Ag detected in organs from highest to lowest is lung>spleen>liver>kidney>thymus>heart. Administration of AgNP induced a marked increase of ALT, BUN, TBil and Cre. Histopathological examination results showed that AgNP induced more extensive organ damages in liver, kidneys, thymus, and spleen. Bone marrow micronucleus assay found no statistical significance among groups (p > 0.05), but the number of aberration cells and multiple aberration cells were predominately increased from rats dosed with Ag(+) and AgNP (p < 0.01), and more polyploidy cells were generated in the AgNP group (4.3%) compared with control. CONCLUSION: Our results indicated that the AgNP accumulated in the immune system organs, and mild irritation was observed in the thymus and spleen of animals treated with AgNP, but not with Ag(+). The liver and kidneys could be the most affected organs by an acute i.v. dose of AgNP, and significantly increased chromosome breakage and polyploidy cell rates also implied the potential genotoxicity of AgNP. However, particle-specific toxicities and potential carcinogenic effect remain to be further confirmed in a chronic toxicity study. |
format | Online Article Text |
id | pubmed-5617228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56172282017-10-09 Acute toxicity and genotoxicity of silver nanoparticle in rats Wen, Hairuo Dan, Mo Yang, Ying Lyu, Jianjun Shao, Anliang Cheng, Xiang Chen, Liang Xu, Liming PLoS One Research Article OBJECTIVE: The potential risk of a nanoparticle as a medical application has raised wide concerns, and this study aims to investigate silver nanoparticle (AgNP)-induced acute toxicities, genotoxicities, target organs and the underlying mechanisms. METHODS: Sprague-Dawley rats were randomly divided into 4 groups (n = 4 each group), and AgNP (containing Ag nanoparticles and released Ag(+), 5 mg/kg), Ag(+) (released from the same dose of AgNP, 0.0003 mg/kg), 5% sucrose solution (vechicle control) and cyclophophamide (positive control, 40 mg/kg) were administrated intravenously for 24 h respectively. Clinical signs and body weight of rats were recorded, and the tissues were subsequently collected for biochemical examination, Ag(+) distribution detection, histopathological examination and genotoxicity assays. RESULTS: The rank of Ag detected in organs from highest to lowest is lung>spleen>liver>kidney>thymus>heart. Administration of AgNP induced a marked increase of ALT, BUN, TBil and Cre. Histopathological examination results showed that AgNP induced more extensive organ damages in liver, kidneys, thymus, and spleen. Bone marrow micronucleus assay found no statistical significance among groups (p > 0.05), but the number of aberration cells and multiple aberration cells were predominately increased from rats dosed with Ag(+) and AgNP (p < 0.01), and more polyploidy cells were generated in the AgNP group (4.3%) compared with control. CONCLUSION: Our results indicated that the AgNP accumulated in the immune system organs, and mild irritation was observed in the thymus and spleen of animals treated with AgNP, but not with Ag(+). The liver and kidneys could be the most affected organs by an acute i.v. dose of AgNP, and significantly increased chromosome breakage and polyploidy cell rates also implied the potential genotoxicity of AgNP. However, particle-specific toxicities and potential carcinogenic effect remain to be further confirmed in a chronic toxicity study. Public Library of Science 2017-09-27 /pmc/articles/PMC5617228/ /pubmed/28953974 http://dx.doi.org/10.1371/journal.pone.0185554 Text en © 2017 Wen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wen, Hairuo Dan, Mo Yang, Ying Lyu, Jianjun Shao, Anliang Cheng, Xiang Chen, Liang Xu, Liming Acute toxicity and genotoxicity of silver nanoparticle in rats |
title | Acute toxicity and genotoxicity of silver nanoparticle in rats |
title_full | Acute toxicity and genotoxicity of silver nanoparticle in rats |
title_fullStr | Acute toxicity and genotoxicity of silver nanoparticle in rats |
title_full_unstemmed | Acute toxicity and genotoxicity of silver nanoparticle in rats |
title_short | Acute toxicity and genotoxicity of silver nanoparticle in rats |
title_sort | acute toxicity and genotoxicity of silver nanoparticle in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617228/ https://www.ncbi.nlm.nih.gov/pubmed/28953974 http://dx.doi.org/10.1371/journal.pone.0185554 |
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