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Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice

INTRODUCTION: Silicon dioxide, produced as synthetic amorphous silica (SAS), is made of nanoparticles (NPs), either present as such or as agglomerates and aggregates, and is widely used in many types of food processes and products as an additive. To assess whether repeated, long-term exposure to SAS...

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Autores principales: Boudard, Delphine, Aureli, Federica, Laurent, Blandine, Sturm, Nathalie, Raggi, Andrea, Antier, Emilie, Lakhdar, Latifa, Marche, Patrice N., Cottier, Michèle, Cubadda, Francesco, Bencsik, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829198/
https://www.ncbi.nlm.nih.gov/pubmed/31701056
http://dx.doi.org/10.1016/j.ekir.2019.06.007
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author Boudard, Delphine
Aureli, Federica
Laurent, Blandine
Sturm, Nathalie
Raggi, Andrea
Antier, Emilie
Lakhdar, Latifa
Marche, Patrice N.
Cottier, Michèle
Cubadda, Francesco
Bencsik, Anna
author_facet Boudard, Delphine
Aureli, Federica
Laurent, Blandine
Sturm, Nathalie
Raggi, Andrea
Antier, Emilie
Lakhdar, Latifa
Marche, Patrice N.
Cottier, Michèle
Cubadda, Francesco
Bencsik, Anna
author_sort Boudard, Delphine
collection PubMed
description INTRODUCTION: Silicon dioxide, produced as synthetic amorphous silica (SAS), is made of nanoparticles (NPs), either present as such or as agglomerates and aggregates, and is widely used in many types of food processes and products as an additive. To assess whether repeated, long-term exposure to SAS NPs may result in adverse effects, mice were exposed for 18 months via drinking water to NM-200, one of the reference nanostructured silica used for applications related to food, at 4.8 mg NM-200/kg body weight per day, a dose relevant to the estimated dietary exposure to SAS in humans. METHODS: The experiment focused on the kidney and liver as target organs and was carried out in parallel using 3 mouse lines (wild type and transgenic) differing for the expression of α-synuclein, that is, murine and human mutated (A53T). Sensitive determination of silicon revealed higher contents in liver and kidneys of NM-200–exposed mice compared with unexposed aged-matched controls. RESULTS: Histological abnormalities, such as vacuolization of tubular epithelial cells, were detected in all kidneys, as well as inflammatory responses that were also detected in livers of exposed animals. Less frequent but more deleterious, amyloidosis lesions were observed in glomeruli, associated with perivascular amyloid accumulation in liver. CONCLUSION: These histological findings, in conjunction with the observation of detectable deposition of silica, highlight that chronic oral intake of SAS may pose a health risk to humans and need to be examined further.
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spelling pubmed-68291982019-11-07 Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice Boudard, Delphine Aureli, Federica Laurent, Blandine Sturm, Nathalie Raggi, Andrea Antier, Emilie Lakhdar, Latifa Marche, Patrice N. Cottier, Michèle Cubadda, Francesco Bencsik, Anna Kidney Int Rep Translational Research INTRODUCTION: Silicon dioxide, produced as synthetic amorphous silica (SAS), is made of nanoparticles (NPs), either present as such or as agglomerates and aggregates, and is widely used in many types of food processes and products as an additive. To assess whether repeated, long-term exposure to SAS NPs may result in adverse effects, mice were exposed for 18 months via drinking water to NM-200, one of the reference nanostructured silica used for applications related to food, at 4.8 mg NM-200/kg body weight per day, a dose relevant to the estimated dietary exposure to SAS in humans. METHODS: The experiment focused on the kidney and liver as target organs and was carried out in parallel using 3 mouse lines (wild type and transgenic) differing for the expression of α-synuclein, that is, murine and human mutated (A53T). Sensitive determination of silicon revealed higher contents in liver and kidneys of NM-200–exposed mice compared with unexposed aged-matched controls. RESULTS: Histological abnormalities, such as vacuolization of tubular epithelial cells, were detected in all kidneys, as well as inflammatory responses that were also detected in livers of exposed animals. Less frequent but more deleterious, amyloidosis lesions were observed in glomeruli, associated with perivascular amyloid accumulation in liver. CONCLUSION: These histological findings, in conjunction with the observation of detectable deposition of silica, highlight that chronic oral intake of SAS may pose a health risk to humans and need to be examined further. Elsevier 2019-06-22 /pmc/articles/PMC6829198/ /pubmed/31701056 http://dx.doi.org/10.1016/j.ekir.2019.06.007 Text en © 2019 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Translational Research
Boudard, Delphine
Aureli, Federica
Laurent, Blandine
Sturm, Nathalie
Raggi, Andrea
Antier, Emilie
Lakhdar, Latifa
Marche, Patrice N.
Cottier, Michèle
Cubadda, Francesco
Bencsik, Anna
Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice
title Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice
title_full Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice
title_fullStr Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice
title_full_unstemmed Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice
title_short Chronic Oral Exposure to Synthetic Amorphous Silica (NM-200) Results in Renal and Liver Lesions in Mice
title_sort chronic oral exposure to synthetic amorphous silica (nm-200) results in renal and liver lesions in mice
topic Translational Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829198/
https://www.ncbi.nlm.nih.gov/pubmed/31701056
http://dx.doi.org/10.1016/j.ekir.2019.06.007
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