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The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice

BACKGROUND: Some herbal natural products play an important role in protecting organisms from the toxic effect of some xenobiotics. The present study was designed to evaluate the potential therapeutic effects of Ottelione A (OTTE) against carbon tetrachloride(CCl(4))-induced toxicity in mice. METHODS...

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Autores principales: Zahran, Rasha Fekry, EL-sayed, Lina Mahmoud, Hoye, Thomas Robert, Ayyad, Seif-Eldin Nasr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511377/
https://www.ncbi.nlm.nih.gov/pubmed/36729297
http://dx.doi.org/10.1007/s12010-023-04346-8
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author Zahran, Rasha Fekry
EL-sayed, Lina Mahmoud
Hoye, Thomas Robert
Ayyad, Seif-Eldin Nasr
author_facet Zahran, Rasha Fekry
EL-sayed, Lina Mahmoud
Hoye, Thomas Robert
Ayyad, Seif-Eldin Nasr
author_sort Zahran, Rasha Fekry
collection PubMed
description BACKGROUND: Some herbal natural products play an important role in protecting organisms from the toxic effect of some xenobiotics. The present study was designed to evaluate the potential therapeutic effects of Ottelione A (OTTE) against carbon tetrachloride(CCl(4))-induced toxicity in mice. METHODS: Adult male Swiss albino mice were divided into six groups: group I was used as a normal control received olive oil; group II received DMSO; group III received OTTE; group IV received CCl(4) in olive oil, (injected i.p) 3 times/week for 6 weeks; group V received the same CCl(4) regimen as group IV followed by OTTE injected for 15 days, and group VI first received OTTE injected for 15 days followed by the same CCl(4) regimen as group IV. Some biochemical and histological parameters were investigated. RESULTS: Our results showed that the administration of CCl(4) caused hepatotoxicity, as monitored by the significant increase in biochemical parameters concerning the olive oil group. Treatment with OTTE appeare d to be effective against hepatotoxic and liver changes induced by CCl(4), as evidenced by the improvement of the same parameters. CONCLUSION: Ottelione A (OTTE) has good antioxidant and therapeutic properties, which can help in preventing CCl(4)-induced hepatotoxicity in both pre-treatment and post-treatment modes. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-105113772023-09-22 The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice Zahran, Rasha Fekry EL-sayed, Lina Mahmoud Hoye, Thomas Robert Ayyad, Seif-Eldin Nasr Appl Biochem Biotechnol Original Article BACKGROUND: Some herbal natural products play an important role in protecting organisms from the toxic effect of some xenobiotics. The present study was designed to evaluate the potential therapeutic effects of Ottelione A (OTTE) against carbon tetrachloride(CCl(4))-induced toxicity in mice. METHODS: Adult male Swiss albino mice were divided into six groups: group I was used as a normal control received olive oil; group II received DMSO; group III received OTTE; group IV received CCl(4) in olive oil, (injected i.p) 3 times/week for 6 weeks; group V received the same CCl(4) regimen as group IV followed by OTTE injected for 15 days, and group VI first received OTTE injected for 15 days followed by the same CCl(4) regimen as group IV. Some biochemical and histological parameters were investigated. RESULTS: Our results showed that the administration of CCl(4) caused hepatotoxicity, as monitored by the significant increase in biochemical parameters concerning the olive oil group. Treatment with OTTE appeare d to be effective against hepatotoxic and liver changes induced by CCl(4), as evidenced by the improvement of the same parameters. CONCLUSION: Ottelione A (OTTE) has good antioxidant and therapeutic properties, which can help in preventing CCl(4)-induced hepatotoxicity in both pre-treatment and post-treatment modes. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2023-02-02 2023 /pmc/articles/PMC10511377/ /pubmed/36729297 http://dx.doi.org/10.1007/s12010-023-04346-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Article
Zahran, Rasha Fekry
EL-sayed, Lina Mahmoud
Hoye, Thomas Robert
Ayyad, Seif-Eldin Nasr
The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice
title The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice
title_full The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice
title_fullStr The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice
title_full_unstemmed The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice
title_short The Dual Therapeutic Potential of Ottelione A on Carbon Tetrachloride-induced Hepatic Toxicity in Mice
title_sort dual therapeutic potential of ottelione a on carbon tetrachloride-induced hepatic toxicity in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511377/
https://www.ncbi.nlm.nih.gov/pubmed/36729297
http://dx.doi.org/10.1007/s12010-023-04346-8
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