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Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats

AIM: The aim of this study is to evaluate the hepatoprotective effect of rutin (RTN) in comparison to silymarin (SLM) against acetaminophen (APAP)-induced hepatotoxicity in rats. MATERIALS AND METHODS: Male Wistar albino rats (n=24) of 3 months age were equally divided into four groups. Group 1 serv...

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Autores principales: Reddy, M. Kasi, Reddy, A. Gopala, Kumar, B. Kala, Madhuri, D., Boobalan, G., Reddy, M. Anudeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Veterinary World 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301182/
https://www.ncbi.nlm.nih.gov/pubmed/28246450
http://dx.doi.org/10.14202/vetworld.2017.74-80
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author Reddy, M. Kasi
Reddy, A. Gopala
Kumar, B. Kala
Madhuri, D.
Boobalan, G.
Reddy, M. Anudeep
author_facet Reddy, M. Kasi
Reddy, A. Gopala
Kumar, B. Kala
Madhuri, D.
Boobalan, G.
Reddy, M. Anudeep
author_sort Reddy, M. Kasi
collection PubMed
description AIM: The aim of this study is to evaluate the hepatoprotective effect of rutin (RTN) in comparison to silymarin (SLM) against acetaminophen (APAP)-induced hepatotoxicity in rats. MATERIALS AND METHODS: Male Wistar albino rats (n=24) of 3 months age were equally divided into four groups. Group 1 served as normal control. Hepatotoxicity was induced in the remaining three groups with administration of 500 mg/kg po APAP from day 1-3. Groups 2, 3, and 4 were subsequently administered orally with distilled water, 25 mg/kg of SLM, and 20 mg/kg of RTN, respectively, for 11 days. The mean body weights and biomarkers of hepatotoxicity were estimated on day 0, 4 (confirmation of toxicity), and 15 (at the end of treatment). Hematological parameters were evaluated on day 4 and 15. Antioxidant profile and adenosine triphosphatases (ATPases) were assessed at the end of the experiment. Liver tissues were subjected to histopathology and transmission electron microscopy after the sacrifice on day 15. RESULTS: Antioxidant profile, ATPases, and hematological and sero-biochemical parameters were significantly altered, and histopathological changes were noticed in the liver of toxic control group. These changes were reversed in groups 3 and 4 that were administered with SLM and RTN, respectively. CONCLUSION: The results of the present investigation enunciated that SLM has potent hepatoprotective activity though the RTN was found superior in restoring the pathological alterations in paracetamol-induced hepatotoxicity in Wistar albino rats.
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spelling pubmed-53011822017-02-28 Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats Reddy, M. Kasi Reddy, A. Gopala Kumar, B. Kala Madhuri, D. Boobalan, G. Reddy, M. Anudeep Vet World Research Article AIM: The aim of this study is to evaluate the hepatoprotective effect of rutin (RTN) in comparison to silymarin (SLM) against acetaminophen (APAP)-induced hepatotoxicity in rats. MATERIALS AND METHODS: Male Wistar albino rats (n=24) of 3 months age were equally divided into four groups. Group 1 served as normal control. Hepatotoxicity was induced in the remaining three groups with administration of 500 mg/kg po APAP from day 1-3. Groups 2, 3, and 4 were subsequently administered orally with distilled water, 25 mg/kg of SLM, and 20 mg/kg of RTN, respectively, for 11 days. The mean body weights and biomarkers of hepatotoxicity were estimated on day 0, 4 (confirmation of toxicity), and 15 (at the end of treatment). Hematological parameters were evaluated on day 4 and 15. Antioxidant profile and adenosine triphosphatases (ATPases) were assessed at the end of the experiment. Liver tissues were subjected to histopathology and transmission electron microscopy after the sacrifice on day 15. RESULTS: Antioxidant profile, ATPases, and hematological and sero-biochemical parameters were significantly altered, and histopathological changes were noticed in the liver of toxic control group. These changes were reversed in groups 3 and 4 that were administered with SLM and RTN, respectively. CONCLUSION: The results of the present investigation enunciated that SLM has potent hepatoprotective activity though the RTN was found superior in restoring the pathological alterations in paracetamol-induced hepatotoxicity in Wistar albino rats. Veterinary World 2017-01 2017-01-19 /pmc/articles/PMC5301182/ /pubmed/28246450 http://dx.doi.org/10.14202/vetworld.2017.74-80 Text en Copyright: © Reddy, et al. http://creativecommons.org/licenses/by/4.0 Open Access. This 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
Reddy, M. Kasi
Reddy, A. Gopala
Kumar, B. Kala
Madhuri, D.
Boobalan, G.
Reddy, M. Anudeep
Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
title Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
title_full Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
title_fullStr Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
title_full_unstemmed Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
title_short Protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
title_sort protective effect of rutin in comparison to silymarin against induced hepatotoxicity in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301182/
https://www.ncbi.nlm.nih.gov/pubmed/28246450
http://dx.doi.org/10.14202/vetworld.2017.74-80
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