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Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics

Iron Oxide Nanoparticles (IONPs) present unique properties making them one of the most used NPs in the biomedical field. Nevertheless, for many years, growing production and use of IONPs are associated with risks that can affect human and the environment. Thus, it is essential to study the effects o...

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Autores principales: Askri, Dalel, Cunin, Valérie, Ouni, Souhir, Béal, David, Rachidi, Walid, Sakly, Mohsen, Amara, Salem, Lehmann, Sylvia G., Sève, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829235/
https://www.ncbi.nlm.nih.gov/pubmed/31635106
http://dx.doi.org/10.3390/ijms20205186
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author Askri, Dalel
Cunin, Valérie
Ouni, Souhir
Béal, David
Rachidi, Walid
Sakly, Mohsen
Amara, Salem
Lehmann, Sylvia G.
Sève, Michel
author_facet Askri, Dalel
Cunin, Valérie
Ouni, Souhir
Béal, David
Rachidi, Walid
Sakly, Mohsen
Amara, Salem
Lehmann, Sylvia G.
Sève, Michel
author_sort Askri, Dalel
collection PubMed
description Iron Oxide Nanoparticles (IONPs) present unique properties making them one of the most used NPs in the biomedical field. Nevertheless, for many years, growing production and use of IONPs are associated with risks that can affect human and the environment. Thus, it is essential to study the effects of these nanoparticles to better understand their mechanism of action and the molecular perturbations induced in the organism. In the present study, we investigated the toxicological effects of IONPs (γ-Fe(2)O(3)) on liver, lung and brain proteomes in Wistar rats. Exposed rats received IONP solution during 7 consecutive days by intranasal instillation at a dose of 10 mg/kg body weight. An iTRAQ-based quantitative proteomics was used to study proteomic variations at the level of the three organs. Using this proteomic approach, we identified 1565; 1135 and 1161 proteins respectively in the brain, liver and lung. Amon them, we quantified 1541; 1125 and 1128 proteins respectively in the brain, liver and lung. Several proteins were dysregulated comparing treated samples to controls, particularly, proteins involved in cytoskeleton remodeling, cellular metabolism, immune system stimulation, inflammation process, response to oxidative stress, angiogenesis, and neurodegenerative diseases.
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spelling pubmed-68292352019-11-18 Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics Askri, Dalel Cunin, Valérie Ouni, Souhir Béal, David Rachidi, Walid Sakly, Mohsen Amara, Salem Lehmann, Sylvia G. Sève, Michel Int J Mol Sci Article Iron Oxide Nanoparticles (IONPs) present unique properties making them one of the most used NPs in the biomedical field. Nevertheless, for many years, growing production and use of IONPs are associated with risks that can affect human and the environment. Thus, it is essential to study the effects of these nanoparticles to better understand their mechanism of action and the molecular perturbations induced in the organism. In the present study, we investigated the toxicological effects of IONPs (γ-Fe(2)O(3)) on liver, lung and brain proteomes in Wistar rats. Exposed rats received IONP solution during 7 consecutive days by intranasal instillation at a dose of 10 mg/kg body weight. An iTRAQ-based quantitative proteomics was used to study proteomic variations at the level of the three organs. Using this proteomic approach, we identified 1565; 1135 and 1161 proteins respectively in the brain, liver and lung. Amon them, we quantified 1541; 1125 and 1128 proteins respectively in the brain, liver and lung. Several proteins were dysregulated comparing treated samples to controls, particularly, proteins involved in cytoskeleton remodeling, cellular metabolism, immune system stimulation, inflammation process, response to oxidative stress, angiogenesis, and neurodegenerative diseases. MDPI 2019-10-19 /pmc/articles/PMC6829235/ /pubmed/31635106 http://dx.doi.org/10.3390/ijms20205186 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Askri, Dalel
Cunin, Valérie
Ouni, Souhir
Béal, David
Rachidi, Walid
Sakly, Mohsen
Amara, Salem
Lehmann, Sylvia G.
Sève, Michel
Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics
title Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics
title_full Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics
title_fullStr Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics
title_full_unstemmed Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics
title_short Effects of Iron Oxide Nanoparticles (γ-Fe(2)O(3)) on Liver, Lung and Brain Proteomes following Sub-Acute Intranasal Exposure: A New Toxicological Assessment in Rat Model Using iTRAQ-Based Quantitative Proteomics
title_sort effects of iron oxide nanoparticles (γ-fe(2)o(3)) on liver, lung and brain proteomes following sub-acute intranasal exposure: a new toxicological assessment in rat model using itraq-based quantitative proteomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829235/
https://www.ncbi.nlm.nih.gov/pubmed/31635106
http://dx.doi.org/10.3390/ijms20205186
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