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Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress
BACKGROUND: Nanoparticles are widely utilized in many products such as cosmetics and sunscreens. The present study was undertaken to evaluate the effect of hesperidin (HSP) on nano zinc oxide particles (nZnO) induced oxidative stress in rat livers. METHODS: Rats were randomly divided into 4 groups o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195725/ https://www.ncbi.nlm.nih.gov/pubmed/30340509 http://dx.doi.org/10.1186/s40360-018-0256-8 |
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author | Ansar, Sabah Abudawood, Manal Alaraj, Amal S. A. Hamed, Sherifa S. |
author_facet | Ansar, Sabah Abudawood, Manal Alaraj, Amal S. A. Hamed, Sherifa S. |
author_sort | Ansar, Sabah |
collection | PubMed |
description | BACKGROUND: Nanoparticles are widely utilized in many products such as cosmetics and sunscreens. The present study was undertaken to evaluate the effect of hesperidin (HSP) on nano zinc oxide particles (nZnO) induced oxidative stress in rat livers. METHODS: Rats were randomly divided into 4 groups of 6 rats each and exposed to single administration of nZnO intraperitoneally (600 mg/kg bwt) and HSP (100 mg/kg bwt) by gavage. Group I served as the control; group II was given nZnO only; groups III received HSP only and group IV received nZnO 1 h after pretreatment with HSP for 7 days. RESULTS: Compared to the controls, nZnO administration enhanced alanine aminotransferase (AST) and aspartate aminotransferase (ALT) levels (p < 0.05) with reduction in the levels of glutathione (GSH), catalase (CAT), glutathione peroxidase (GPx), superoxide dismutase (SOD) and increase in levels of malondialdehyde (MDA) while HSP attenuated nZnO-induced hepatotoxicity for above mentioned parameters. CONCLUSIONS: The induced toxicity in the liver was corrected by pretreatment with HSP. The findings of this study suggest that HSP pretreatment can potentially be used to prevent nZnO-induced biochemical alterations toxicity. Further, protection by HSP on biochemical results was confirmed by histopathological changes. The present study suggests that HSP can protect against nZnO-induced oxidative damage in the rat livers. |
format | Online Article Text |
id | pubmed-6195725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61957252018-10-30 Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress Ansar, Sabah Abudawood, Manal Alaraj, Amal S. A. Hamed, Sherifa S. BMC Pharmacol Toxicol Research Article BACKGROUND: Nanoparticles are widely utilized in many products such as cosmetics and sunscreens. The present study was undertaken to evaluate the effect of hesperidin (HSP) on nano zinc oxide particles (nZnO) induced oxidative stress in rat livers. METHODS: Rats were randomly divided into 4 groups of 6 rats each and exposed to single administration of nZnO intraperitoneally (600 mg/kg bwt) and HSP (100 mg/kg bwt) by gavage. Group I served as the control; group II was given nZnO only; groups III received HSP only and group IV received nZnO 1 h after pretreatment with HSP for 7 days. RESULTS: Compared to the controls, nZnO administration enhanced alanine aminotransferase (AST) and aspartate aminotransferase (ALT) levels (p < 0.05) with reduction in the levels of glutathione (GSH), catalase (CAT), glutathione peroxidase (GPx), superoxide dismutase (SOD) and increase in levels of malondialdehyde (MDA) while HSP attenuated nZnO-induced hepatotoxicity for above mentioned parameters. CONCLUSIONS: The induced toxicity in the liver was corrected by pretreatment with HSP. The findings of this study suggest that HSP pretreatment can potentially be used to prevent nZnO-induced biochemical alterations toxicity. Further, protection by HSP on biochemical results was confirmed by histopathological changes. The present study suggests that HSP can protect against nZnO-induced oxidative damage in the rat livers. BioMed Central 2018-10-19 /pmc/articles/PMC6195725/ /pubmed/30340509 http://dx.doi.org/10.1186/s40360-018-0256-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ansar, Sabah Abudawood, Manal Alaraj, Amal S. A. Hamed, Sherifa S. Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
title | Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
title_full | Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
title_fullStr | Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
title_full_unstemmed | Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
title_short | Hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
title_sort | hesperidin alleviates zinc oxide nanoparticle induced hepatotoxicity and oxidative stress |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195725/ https://www.ncbi.nlm.nih.gov/pubmed/30340509 http://dx.doi.org/10.1186/s40360-018-0256-8 |
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