The effect of ZnO nanoparticles on liver function in rats

Hua-Qiao Tang, Min Xu, Qian Rong, Ru-Wen Jin, Qi-Ji Liu, Ying-Lun Li Department of Pharmacy, Sichuan Agricultural University, Sichuan, Chengdu, People’s Republic of China Abstract: Zinc oxide (ZnO) is widely incorporated as a food additive in animal diets. In order to optimize the benefi...

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Autores principales: Tang HQ, Xu M, Rong Q, Jin RW, Liu QJ, Li YL
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Publicado: Dove Medical Press 2016
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spelling oai:doaj.org-article:495cdb8ecafa40738ab138955adad11f2021-12-02T00:45:57ZThe effect of ZnO nanoparticles on liver function in rats1178-2013https://doaj.org/article/495cdb8ecafa40738ab138955adad11f2016-08-01T00:00:00Zhttps://www.dovepress.com/the-effect-of-zno-nanoparticles-on-liver-function-in-rats-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Hua-Qiao Tang, Min Xu, Qian Rong, Ru-Wen Jin, Qi-Ji Liu, Ying-Lun Li Department of Pharmacy, Sichuan Agricultural University, Sichuan, Chengdu, People’s Republic of China Abstract: 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. Keywords: ZnO nanoparticles, liver injury, CYP450 enzymesTang HQXu MRong QJin RWLiu QJLi YLDove Medical PressarticleZnO nanoparticlesliver injuryCYP 450 enzymesMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 11, Pp 4275-4285 (2016)
institution DOAJ
collection DOAJ
language EN
topic ZnO nanoparticles
liver injury
CYP 450 enzymes
Medicine (General)
R5-920
spellingShingle ZnO nanoparticles
liver injury
CYP 450 enzymes
Medicine (General)
R5-920
Tang HQ
Xu M
Rong Q
Jin RW
Liu QJ
Li YL
The effect of ZnO nanoparticles on liver function in rats
description Hua-Qiao Tang, Min Xu, Qian Rong, Ru-Wen Jin, Qi-Ji Liu, Ying-Lun Li Department of Pharmacy, Sichuan Agricultural University, Sichuan, Chengdu, People’s Republic of China Abstract: 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. Keywords: ZnO nanoparticles, liver injury, CYP450 enzymes
format article
author Tang HQ
Xu M
Rong Q
Jin RW
Liu QJ
Li YL
author_facet Tang HQ
Xu M
Rong Q
Jin RW
Liu QJ
Li YL
author_sort Tang HQ
title The effect of ZnO nanoparticles on liver function in rats
title_short 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_sort effect of zno nanoparticles on liver function in rats
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/495cdb8ecafa40738ab138955adad11f
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