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An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats

OBJECTIVE: The current work was aimed to evaluate the nephroprotective potential of Butea monosperma. MATERIALS AND METHODS: Butea monosperma was collected from local forest of Jabalpur and extracted with ethanol. Healthy adult male Wistar albino rats between 5 and 6 months of age and weighing about...

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Autores principales: Sonkar, Nisha, Ganeshpurkar, Aditya, Yadav, Priyanka, Dubey, Shagun, Bansal, Divya, Dubey, Nazneen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912793/
https://www.ncbi.nlm.nih.gov/pubmed/24550595
http://dx.doi.org/10.4103/0253-7613.125190
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author Sonkar, Nisha
Ganeshpurkar, Aditya
Yadav, Priyanka
Dubey, Shagun
Bansal, Divya
Dubey, Nazneen
author_facet Sonkar, Nisha
Ganeshpurkar, Aditya
Yadav, Priyanka
Dubey, Shagun
Bansal, Divya
Dubey, Nazneen
author_sort Sonkar, Nisha
collection PubMed
description OBJECTIVE: The current work was aimed to evaluate the nephroprotective potential of Butea monosperma. MATERIALS AND METHODS: Butea monosperma was collected from local forest of Jabalpur and extracted with ethanol. Healthy adult male Wistar albino rats between 5 and 6 months of age and weighing about 150-200 g were used for the study. Acute toxicity studies were performed to determine dose of extract. Nephrotoxicity was induced by gentamicin. Animals were divided in four groups in which first group served as positive control, second group as gentamicin treated toxic control; animals of group three and four were treated with Butea monosperma extract. Extract was administered to animals via oral route. Serum creatinine, serum urea, and blood urea nitrogen were estimated. Body weight was also determined. Histopathological studies were performed to access gross anatomical changes in animals. RESULTS: The extract of Butea monosperma was found to be rich in flavonoids, polyphenolics, and alkaloids. Urine creatinine, serum urea, and blood urea nitrogen were found to be significantly (P < 0.001) increased in rats treated with only gentamicin; whereas, treatment with the ethanolic extract of leaf of Butea monosperma reversed the effect of gentamicin indicating nephroprotective activity. CONCLUSION: The present study revealed that ethanolic extract of Butea monosperma is a good source of phytochemicals. The phytoconstituents flavonoids, phenolics, and alkaloids present in the extracts may be responsible for antioxidant activity. By the virtue of antioxidant activity, Butea monosperma demonstrated nephroprotective activity.
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spelling pubmed-39127932014-02-18 An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats Sonkar, Nisha Ganeshpurkar, Aditya Yadav, Priyanka Dubey, Shagun Bansal, Divya Dubey, Nazneen Indian J Pharmacol Short Communication OBJECTIVE: The current work was aimed to evaluate the nephroprotective potential of Butea monosperma. MATERIALS AND METHODS: Butea monosperma was collected from local forest of Jabalpur and extracted with ethanol. Healthy adult male Wistar albino rats between 5 and 6 months of age and weighing about 150-200 g were used for the study. Acute toxicity studies were performed to determine dose of extract. Nephrotoxicity was induced by gentamicin. Animals were divided in four groups in which first group served as positive control, second group as gentamicin treated toxic control; animals of group three and four were treated with Butea monosperma extract. Extract was administered to animals via oral route. Serum creatinine, serum urea, and blood urea nitrogen were estimated. Body weight was also determined. Histopathological studies were performed to access gross anatomical changes in animals. RESULTS: The extract of Butea monosperma was found to be rich in flavonoids, polyphenolics, and alkaloids. Urine creatinine, serum urea, and blood urea nitrogen were found to be significantly (P < 0.001) increased in rats treated with only gentamicin; whereas, treatment with the ethanolic extract of leaf of Butea monosperma reversed the effect of gentamicin indicating nephroprotective activity. CONCLUSION: The present study revealed that ethanolic extract of Butea monosperma is a good source of phytochemicals. The phytoconstituents flavonoids, phenolics, and alkaloids present in the extracts may be responsible for antioxidant activity. By the virtue of antioxidant activity, Butea monosperma demonstrated nephroprotective activity. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3912793/ /pubmed/24550595 http://dx.doi.org/10.4103/0253-7613.125190 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Sonkar, Nisha
Ganeshpurkar, Aditya
Yadav, Priyanka
Dubey, Shagun
Bansal, Divya
Dubey, Nazneen
An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats
title An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats
title_full An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats
title_fullStr An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats
title_full_unstemmed An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats
title_short An experimetal evaluation of nephroprotective potential of Butea monosperma extract in albino rats
title_sort experimetal evaluation of nephroprotective potential of butea monosperma extract in albino rats
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912793/
https://www.ncbi.nlm.nih.gov/pubmed/24550595
http://dx.doi.org/10.4103/0253-7613.125190
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