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Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats

Hepatitis is one of earlier, but serious, signs of liver damage. High doses of statins for a long time can induce hepatitis. This study aimed to evaluate and compare the therapeutic potential of thymoquinone (TQ) and bee pollen (BP) on fluvastatin (F)-induced hepatitis in rats. Rats were randomly di...

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Autores principales: Mohamed, Amro E., El-Magd, Mohammed A., El-Said, Karim S., El-Sharnouby, Mohamed, Tousson, Ehab M., Salama, Afrah F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333355/
https://www.ncbi.nlm.nih.gov/pubmed/34344946
http://dx.doi.org/10.1038/s41598-021-95342-7
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author Mohamed, Amro E.
El-Magd, Mohammed A.
El-Said, Karim S.
El-Sharnouby, Mohamed
Tousson, Ehab M.
Salama, Afrah F.
author_facet Mohamed, Amro E.
El-Magd, Mohammed A.
El-Said, Karim S.
El-Sharnouby, Mohamed
Tousson, Ehab M.
Salama, Afrah F.
author_sort Mohamed, Amro E.
collection PubMed
description Hepatitis is one of earlier, but serious, signs of liver damage. High doses of statins for a long time can induce hepatitis. This study aimed to evaluate and compare the therapeutic potential of thymoquinone (TQ) and bee pollen (BP) on fluvastatin (F)-induced hepatitis in rats. Rats were randomly divided into: group 1 (G1, control), G2 (F, hepatitis), G3 (F + TQ), G4 (F + BP), and G5 (F + TQ + BP). Single treatment with TQ or BP relieved fluvastatin-induced hepatitis, with best effect for the combined therapy. TQ and/or BP treatment significantly (1) reduced serum levels of alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma glutamyl transpeptidase, and total bilirubin, (2) decreased malondialdehyde levels and increased level of reduced glutathione, and activities of glutathione peroxidase and catalase in the liver, (3) improved liver histology with mild deposition of type I collagen, (4) increased mRNA levels of transforming growth factor beta 1, nuclear factor Kappa B, and cyclooxygenase 1 and 2, and (5) decreased tumor necrosis factor alpha and upregulated interleukin 10 protein in the liver. These data clearly highlight the ability of TQ and BP combined therapy to cause better ameliorative effects on fluvastatin-induced hepatitis than individual treatment by each alone.
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spelling pubmed-83333552021-08-05 Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats Mohamed, Amro E. El-Magd, Mohammed A. El-Said, Karim S. El-Sharnouby, Mohamed Tousson, Ehab M. Salama, Afrah F. Sci Rep Article Hepatitis is one of earlier, but serious, signs of liver damage. High doses of statins for a long time can induce hepatitis. This study aimed to evaluate and compare the therapeutic potential of thymoquinone (TQ) and bee pollen (BP) on fluvastatin (F)-induced hepatitis in rats. Rats were randomly divided into: group 1 (G1, control), G2 (F, hepatitis), G3 (F + TQ), G4 (F + BP), and G5 (F + TQ + BP). Single treatment with TQ or BP relieved fluvastatin-induced hepatitis, with best effect for the combined therapy. TQ and/or BP treatment significantly (1) reduced serum levels of alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma glutamyl transpeptidase, and total bilirubin, (2) decreased malondialdehyde levels and increased level of reduced glutathione, and activities of glutathione peroxidase and catalase in the liver, (3) improved liver histology with mild deposition of type I collagen, (4) increased mRNA levels of transforming growth factor beta 1, nuclear factor Kappa B, and cyclooxygenase 1 and 2, and (5) decreased tumor necrosis factor alpha and upregulated interleukin 10 protein in the liver. These data clearly highlight the ability of TQ and BP combined therapy to cause better ameliorative effects on fluvastatin-induced hepatitis than individual treatment by each alone. Nature Publishing Group UK 2021-08-03 /pmc/articles/PMC8333355/ /pubmed/34344946 http://dx.doi.org/10.1038/s41598-021-95342-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mohamed, Amro E.
El-Magd, Mohammed A.
El-Said, Karim S.
El-Sharnouby, Mohamed
Tousson, Ehab M.
Salama, Afrah F.
Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
title Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
title_full Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
title_fullStr Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
title_full_unstemmed Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
title_short Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
title_sort potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333355/
https://www.ncbi.nlm.nih.gov/pubmed/34344946
http://dx.doi.org/10.1038/s41598-021-95342-7
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