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Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats

INTRODUCTION: The root of Plumbago zeylanica Linn. is used in traditional medicine for the treatment of chronic inflammatory diseases and various disorders. The toxicity of this plant has not yet been extensively evaluated. AIM: To evaluate and compare the toxicity of P. zeylanica root petroleum eth...

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Autores principales: Kumar, Dushyant, Patil, Paragouda A., Roy, Subarna, Kholkute, Sanjiv D., Hegde, Harsha V., Nair, Vinod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895762/
https://www.ncbi.nlm.nih.gov/pubmed/27313422
http://dx.doi.org/10.4103/0974-8520.182750
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author Kumar, Dushyant
Patil, Paragouda A.
Roy, Subarna
Kholkute, Sanjiv D.
Hegde, Harsha V.
Nair, Vinod
author_facet Kumar, Dushyant
Patil, Paragouda A.
Roy, Subarna
Kholkute, Sanjiv D.
Hegde, Harsha V.
Nair, Vinod
author_sort Kumar, Dushyant
collection PubMed
description INTRODUCTION: The root of Plumbago zeylanica Linn. is used in traditional medicine for the treatment of chronic inflammatory diseases and various disorders. The toxicity of this plant has not yet been extensively evaluated. AIM: To evaluate and compare the toxicity of P. zeylanica root petroleum ether (PZPE), acetone (PZAC), and the hydroalcoholic (PZHY) extracts. MATERIALS AND METHODS: The acute and sub-acute toxicities of extracts were evaluated according to OECD guidelines 425 and 407, respectively in female rats. RESULTS: PZPE was more toxic than PZAC and PZHA, based on LD50 values of 93.45, 928.4, and 928.4 mg/kg, respectively. This potency difference directly correlates with the plumbagin content of extracts. With regard to sub-acute toxicity, a significant increase in organ weights (liver, adrenal glands, and/or heart) was observed in PZPE and PZAC treated groups. All extracts produced a significant increase in serum aspartate aminotransferase and urea, and PZAC produced a significant increase in serum creatinine as compared to control. A decrease in hematocrit was observed in the highest dose PZPE group, and a decrease in leukocytes was observed in all PZAC groups. Hepatic and renal changes were observed in all extract treated groups. CONCLUSION: The findings of our study, thus demonstrate that liver and kidney are the primary organs being adversely affected following sub-acute administration of P. zeylanica root extract in rats.
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spelling pubmed-48957622016-06-16 Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats Kumar, Dushyant Patil, Paragouda A. Roy, Subarna Kholkute, Sanjiv D. Hegde, Harsha V. Nair, Vinod Ayu Pharmacological Study INTRODUCTION: The root of Plumbago zeylanica Linn. is used in traditional medicine for the treatment of chronic inflammatory diseases and various disorders. The toxicity of this plant has not yet been extensively evaluated. AIM: To evaluate and compare the toxicity of P. zeylanica root petroleum ether (PZPE), acetone (PZAC), and the hydroalcoholic (PZHY) extracts. MATERIALS AND METHODS: The acute and sub-acute toxicities of extracts were evaluated according to OECD guidelines 425 and 407, respectively in female rats. RESULTS: PZPE was more toxic than PZAC and PZHA, based on LD50 values of 93.45, 928.4, and 928.4 mg/kg, respectively. This potency difference directly correlates with the plumbagin content of extracts. With regard to sub-acute toxicity, a significant increase in organ weights (liver, adrenal glands, and/or heart) was observed in PZPE and PZAC treated groups. All extracts produced a significant increase in serum aspartate aminotransferase and urea, and PZAC produced a significant increase in serum creatinine as compared to control. A decrease in hematocrit was observed in the highest dose PZPE group, and a decrease in leukocytes was observed in all PZAC groups. Hepatic and renal changes were observed in all extract treated groups. CONCLUSION: The findings of our study, thus demonstrate that liver and kidney are the primary organs being adversely affected following sub-acute administration of P. zeylanica root extract in rats. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4895762/ /pubmed/27313422 http://dx.doi.org/10.4103/0974-8520.182750 Text en Copyright: © AYU (An International Quarterly Journal of Research in Ayurveda) 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Pharmacological Study
Kumar, Dushyant
Patil, Paragouda A.
Roy, Subarna
Kholkute, Sanjiv D.
Hegde, Harsha V.
Nair, Vinod
Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats
title Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats
title_full Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats
title_fullStr Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats
title_full_unstemmed Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats
title_short Comparative toxicity profiles of Plumbago zeylanica L. root petroleum ether, acetone and hydroalcoholic extracts in Wistar rats
title_sort comparative toxicity profiles of plumbago zeylanica l. root petroleum ether, acetone and hydroalcoholic extracts in wistar rats
topic Pharmacological Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895762/
https://www.ncbi.nlm.nih.gov/pubmed/27313422
http://dx.doi.org/10.4103/0974-8520.182750
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