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The effect of ZnO nanoparticles on liver function in rats

Zinc oxide (ZnO) is widely incorporated as a food additive in animal diets. In order to optimize the beneficial effects of ZnO and minimize any resultant environmental pollution, ZnO nanoparticles are often used for delivery of the zinc. However, the possible toxic effects of ZnO nanoparticles, incl...

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Autores principales: Tang, Hua-Qiao, Xu, Min, Rong, Qian, Jin, Ru-Wen, Liu, Qi-Ji, Li, Ying-Lun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012617/
https://www.ncbi.nlm.nih.gov/pubmed/27621621
http://dx.doi.org/10.2147/IJN.S109031
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author Tang, Hua-Qiao
Xu, Min
Rong, Qian
Jin, Ru-Wen
Liu, Qi-Ji
Li, Ying-Lun
author_facet Tang, Hua-Qiao
Xu, Min
Rong, Qian
Jin, Ru-Wen
Liu, Qi-Ji
Li, Ying-Lun
author_sort Tang, Hua-Qiao
collection PubMed
description Zinc oxide (ZnO) is widely incorporated as a food additive in animal diets. In order to optimize the beneficial effects of ZnO and minimize any resultant environmental pollution, ZnO nanoparticles are often used for delivery of the zinc. However, the possible toxic effects of ZnO nanoparticles, including effects on cytochrome P450 (CYP450) enzymes, have not been evaluated. In this study, we investigated the effect of ZnO nanoparticles, in doses used in animal feeds, on CYP450 enzymes, liver and intestinal enzymes, liver and kidney histopathology, and hematologic indices in rats. We found that liver and kidney injury occurred when the concentrations of ZnO nanoparticles in feed were 300–600 mg/kg. Also, liver mRNA expression for constitutive androstane receptor was suppressed and mRNA expression for pregnane X receptor was induced when feed containing ZnO nanoparticles was given at a concentration of 600 mg/kg. Although the expression of mRNA for CYP 2C11 and 3A2 enzymes was induced by ZnO nanoparticles, the activities of CYP 2C11 and 3A2 were suppressed. While liver CYP 1A2 mRNA expression was suppressed, CYP 1A2 activity remained unchanged at all ZnO nanoparticle doses. Therefore, it has been concluded that ZnO nanoparticles, in the doses customarily added to animal feed, changed the indices of hematology and blood chemistry, altered the expression and activity of hepatic CYP enzymes, and induced pathological changes in liver and kidney tissues of rats. These findings suggest that greater attention needs to be paid to the toxic effects of ZnO nanoparticles in animal feed, with the possibility that the doses of ZnO should be reduced.
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spelling pubmed-50126172016-09-12 The effect of ZnO nanoparticles on liver function in rats Tang, Hua-Qiao Xu, Min Rong, Qian Jin, Ru-Wen Liu, Qi-Ji Li, Ying-Lun Int J Nanomedicine Original Research Zinc oxide (ZnO) is widely incorporated as a food additive in animal diets. In order to optimize the beneficial effects of ZnO and minimize any resultant environmental pollution, ZnO nanoparticles are often used for delivery of the zinc. However, the possible toxic effects of ZnO nanoparticles, including effects on cytochrome P450 (CYP450) enzymes, have not been evaluated. In this study, we investigated the effect of ZnO nanoparticles, in doses used in animal feeds, on CYP450 enzymes, liver and intestinal enzymes, liver and kidney histopathology, and hematologic indices in rats. We found that liver and kidney injury occurred when the concentrations of ZnO nanoparticles in feed were 300–600 mg/kg. Also, liver mRNA expression for constitutive androstane receptor was suppressed and mRNA expression for pregnane X receptor was induced when feed containing ZnO nanoparticles was given at a concentration of 600 mg/kg. Although the expression of mRNA for CYP 2C11 and 3A2 enzymes was induced by ZnO nanoparticles, the activities of CYP 2C11 and 3A2 were suppressed. While liver CYP 1A2 mRNA expression was suppressed, CYP 1A2 activity remained unchanged at all ZnO nanoparticle doses. Therefore, it has been concluded that ZnO nanoparticles, in the doses customarily added to animal feed, changed the indices of hematology and blood chemistry, altered the expression and activity of hepatic CYP enzymes, and induced pathological changes in liver and kidney tissues of rats. These findings suggest that greater attention needs to be paid to the toxic effects of ZnO nanoparticles in animal feed, with the possibility that the doses of ZnO should be reduced. Dove Medical Press 2016-08-31 /pmc/articles/PMC5012617/ /pubmed/27621621 http://dx.doi.org/10.2147/IJN.S109031 Text en © 2016 Tang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Tang, Hua-Qiao
Xu, Min
Rong, Qian
Jin, Ru-Wen
Liu, Qi-Ji
Li, Ying-Lun
The effect of ZnO nanoparticles on liver function in rats
title The effect of ZnO nanoparticles on liver function in rats
title_full The effect of ZnO nanoparticles on liver function in rats
title_fullStr The effect of ZnO nanoparticles on liver function in rats
title_full_unstemmed The effect of ZnO nanoparticles on liver function in rats
title_short The effect of ZnO nanoparticles on liver function in rats
title_sort effect of zno nanoparticles on liver function in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012617/
https://www.ncbi.nlm.nih.gov/pubmed/27621621
http://dx.doi.org/10.2147/IJN.S109031
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