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EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS

Insight of evidence that some complications of diabetes mellitus due to hyperglycemia, we investigated the effect of T. arjuna bark extract on serum, liver and kidney marker enzymes in alloxan - induced diabetic rats. T. arjuna was administered orally at a doses of 250 and 500 mg/kg body weight for...

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Detalles Bibliográficos
Autores principales: Ragavan, B., Krishnakumari, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3330897/
https://www.ncbi.nlm.nih.gov/pubmed/22557182
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author Ragavan, B.
Krishnakumari, S.
author_facet Ragavan, B.
Krishnakumari, S.
author_sort Ragavan, B.
collection PubMed
description Insight of evidence that some complications of diabetes mellitus due to hyperglycemia, we investigated the effect of T. arjuna bark extract on serum, liver and kidney marker enzymes in alloxan - induced diabetic rats. T. arjuna was administered orally at a doses of 250 and 500 mg/kg body weight for 30 days, after which serum liver and kidney tissues were assayed for the degree of pathological changes by means of markers such as alkaline phosphatase (ALP), acid phosphatase (ACP), alanine amino transferase (ALT), aspartate amino transferase (AST) and lactate dehydrogenase (LDH) resulted in a significant reduction in serum and tissue of liver and kidney marker enzymes when compared with control rats T. arjuna at a dose of 500 mg/kg body weight exhibited higher efficacy.
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spelling pubmed-33308972012-04-27 EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS Ragavan, B. Krishnakumari, S. Anc Sci Life Original Article Insight of evidence that some complications of diabetes mellitus due to hyperglycemia, we investigated the effect of T. arjuna bark extract on serum, liver and kidney marker enzymes in alloxan - induced diabetic rats. T. arjuna was administered orally at a doses of 250 and 500 mg/kg body weight for 30 days, after which serum liver and kidney tissues were assayed for the degree of pathological changes by means of markers such as alkaline phosphatase (ALP), acid phosphatase (ACP), alanine amino transferase (ALT), aspartate amino transferase (AST) and lactate dehydrogenase (LDH) resulted in a significant reduction in serum and tissue of liver and kidney marker enzymes when compared with control rats T. arjuna at a dose of 500 mg/kg body weight exhibited higher efficacy. Medknow Publications & Media Pvt Ltd 2005 /pmc/articles/PMC3330897/ /pubmed/22557182 Text en Copyright: © Ancient Science of Life 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 Original Article
Ragavan, B.
Krishnakumari, S.
EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS
title EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS
title_full EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS
title_fullStr EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS
title_full_unstemmed EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS
title_short EFFECT OF TERMINALIA ARJUNA STEM BARK EXTRACT ON THE ACTIVITIES OF MARKER ENZYMES IN ALLOXAN INDUCED DIABETIC RATS
title_sort effect of terminalia arjuna stem bark extract on the activities of marker enzymes in alloxan induced diabetic rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3330897/
https://www.ncbi.nlm.nih.gov/pubmed/22557182
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