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Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2

The presented study was performed to verify whether rutin and/or quercetin can inhibit liver injury induced by doxorubicin (DXR) in male Wistar rats. In this study, male Wistar rats were treated via the oral route with rutin and quercetin (50 mg/kg) either alone or in combination every other day for...

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Autores principales: Ahmed, Osama M., Elkomy, Mohammed H., Fahim, Hanaa I., Ashour, Mohamed B., Naguib, Ibrahim A., Alghamdi, Badrah S., Mahmoud, Heba Uallah R., Ahmed, Noha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348941/
https://www.ncbi.nlm.nih.gov/pubmed/35936216
http://dx.doi.org/10.1155/2022/2710607
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author Ahmed, Osama M.
Elkomy, Mohammed H.
Fahim, Hanaa I.
Ashour, Mohamed B.
Naguib, Ibrahim A.
Alghamdi, Badrah S.
Mahmoud, Heba Uallah R.
Ahmed, Noha A.
author_facet Ahmed, Osama M.
Elkomy, Mohammed H.
Fahim, Hanaa I.
Ashour, Mohamed B.
Naguib, Ibrahim A.
Alghamdi, Badrah S.
Mahmoud, Heba Uallah R.
Ahmed, Noha A.
author_sort Ahmed, Osama M.
collection PubMed
description The presented study was performed to verify whether rutin and/or quercetin can inhibit liver injury induced by doxorubicin (DXR) in male Wistar rats. In this study, male Wistar rats were treated via the oral route with rutin and quercetin (50 mg/kg) either alone or in combination every other day for five weeks concomitant with receiving intraperitoneal DXR (2 mg/kg) two times a week for five successive weeks. Quercetin, rutin, and their combination significantly improved the deteriorated serum AST, ALT, and ALP activities and total bilirubin level, as well as albumin, AFP, and CA 19.9 levels in DXR-injected rats. Treatments of the DXR-injected group with quercetin and rutin prevented the elevation in liver lipid peroxidation and the reduction in superoxide dismutase, glutathione-S-transferase and glutathione peroxidase activities, and glutathione content. Treatments with quercetin and rutin significantly repressed the elevated expression of liver p53 and TNF-α and enhanced Nrf2 expression. Furthermore, the treatments significantly reduced DXR-induced liver histological changes. In conclusion, rutin and quercetin either alone or in combination may have potential preventive effects against DXR-induced hepatotoxicity through inhibiting oxidative stress, inflammation, and apoptosis as well as modulating the Nrf2 expression.
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spelling pubmed-93489412022-08-04 Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2 Ahmed, Osama M. Elkomy, Mohammed H. Fahim, Hanaa I. Ashour, Mohamed B. Naguib, Ibrahim A. Alghamdi, Badrah S. Mahmoud, Heba Uallah R. Ahmed, Noha A. Oxid Med Cell Longev Research Article The presented study was performed to verify whether rutin and/or quercetin can inhibit liver injury induced by doxorubicin (DXR) in male Wistar rats. In this study, male Wistar rats were treated via the oral route with rutin and quercetin (50 mg/kg) either alone or in combination every other day for five weeks concomitant with receiving intraperitoneal DXR (2 mg/kg) two times a week for five successive weeks. Quercetin, rutin, and their combination significantly improved the deteriorated serum AST, ALT, and ALP activities and total bilirubin level, as well as albumin, AFP, and CA 19.9 levels in DXR-injected rats. Treatments of the DXR-injected group with quercetin and rutin prevented the elevation in liver lipid peroxidation and the reduction in superoxide dismutase, glutathione-S-transferase and glutathione peroxidase activities, and glutathione content. Treatments with quercetin and rutin significantly repressed the elevated expression of liver p53 and TNF-α and enhanced Nrf2 expression. Furthermore, the treatments significantly reduced DXR-induced liver histological changes. In conclusion, rutin and quercetin either alone or in combination may have potential preventive effects against DXR-induced hepatotoxicity through inhibiting oxidative stress, inflammation, and apoptosis as well as modulating the Nrf2 expression. Hindawi 2022-07-27 /pmc/articles/PMC9348941/ /pubmed/35936216 http://dx.doi.org/10.1155/2022/2710607 Text en Copyright © 2022 Osama M. Ahmed et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ahmed, Osama M.
Elkomy, Mohammed H.
Fahim, Hanaa I.
Ashour, Mohamed B.
Naguib, Ibrahim A.
Alghamdi, Badrah S.
Mahmoud, Heba Uallah R.
Ahmed, Noha A.
Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2
title Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2
title_full Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2
title_fullStr Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2
title_full_unstemmed Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2
title_short Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2
title_sort rutin and quercetin counter doxorubicin-induced liver toxicity in wistar rats via their modulatory effects on inflammation, oxidative stress, apoptosis, and nrf2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348941/
https://www.ncbi.nlm.nih.gov/pubmed/35936216
http://dx.doi.org/10.1155/2022/2710607
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