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Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna

Arjuna Ksheera Paka (AKP), a traditional Ayurvedic formulation of Terminalia arjuna (T. arjuna) bark powder is used for its cardioprotective effects. However, its anti-inflammatory efficacy remained unexplored. In the present study, AKP was prepared in cow milk (as per standard Ayurvedic procedure)...

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Autores principales: Dube, Nivedita, Nimgulkar, Chetan, Bharatraj, Dinesh Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634724/
https://www.ncbi.nlm.nih.gov/pubmed/29034188
http://dx.doi.org/10.1016/j.jtcme.2016.11.006
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author Dube, Nivedita
Nimgulkar, Chetan
Bharatraj, Dinesh Kumar
author_facet Dube, Nivedita
Nimgulkar, Chetan
Bharatraj, Dinesh Kumar
author_sort Dube, Nivedita
collection PubMed
description Arjuna Ksheera Paka (AKP), a traditional Ayurvedic formulation of Terminalia arjuna (T. arjuna) bark powder is used for its cardioprotective effects. However, its anti-inflammatory efficacy remained unexplored. In the present study, AKP was prepared in cow milk (as per standard Ayurvedic procedure) and compared with standard hydroalcoholic extract (HA) of T. arjuna. The extracts were analyzed for gross phytoconstituents levels, and their antioxidant activity was assayed by DPPH free radical scavenging activity and inhibition of lipid peroxidation. The in vivo anti-inflammatory activity of AKP and HA was studied in carrageenan-induced hind paw biphasic edema in C57BL/6 mice (at 200, 400 and 800 mg/kg BW). The percentage extraction yield of AKP was two folds higher than HA implying that the phytoconstituents in AKP were diluted by a factor of 0.5. The total polyphenol content of HA was (3.8 times) higher than AKP and the antioxidant activity of HA was also higher compared to AKP. Both the extracts, however, showed significant (p < 0.05) anti-inflammatory activity in reducing paw edema in mice. The efficacy of HA was more than AKP at early phase of inflammation, whereas, in the late phase of inflammation AKP was more efficacious and equipotent to HA. Thus, regardless of low in vitro antioxidant activity, AKP exhibited potential in vivo anti-inflammatory activity. The higher efficacy of AKP could be due to the presence of milk solids. These milk solids may act as adjuvants to T. arjuna's phytoconstituents, contributing to their sustained bioavailability, leading to higher in vivo anti-inflammatory efficacy at lower drug concentrations.
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spelling pubmed-56347242017-10-13 Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna Dube, Nivedita Nimgulkar, Chetan Bharatraj, Dinesh Kumar J Tradit Complement Med Original Article Arjuna Ksheera Paka (AKP), a traditional Ayurvedic formulation of Terminalia arjuna (T. arjuna) bark powder is used for its cardioprotective effects. However, its anti-inflammatory efficacy remained unexplored. In the present study, AKP was prepared in cow milk (as per standard Ayurvedic procedure) and compared with standard hydroalcoholic extract (HA) of T. arjuna. The extracts were analyzed for gross phytoconstituents levels, and their antioxidant activity was assayed by DPPH free radical scavenging activity and inhibition of lipid peroxidation. The in vivo anti-inflammatory activity of AKP and HA was studied in carrageenan-induced hind paw biphasic edema in C57BL/6 mice (at 200, 400 and 800 mg/kg BW). The percentage extraction yield of AKP was two folds higher than HA implying that the phytoconstituents in AKP were diluted by a factor of 0.5. The total polyphenol content of HA was (3.8 times) higher than AKP and the antioxidant activity of HA was also higher compared to AKP. Both the extracts, however, showed significant (p < 0.05) anti-inflammatory activity in reducing paw edema in mice. The efficacy of HA was more than AKP at early phase of inflammation, whereas, in the late phase of inflammation AKP was more efficacious and equipotent to HA. Thus, regardless of low in vitro antioxidant activity, AKP exhibited potential in vivo anti-inflammatory activity. The higher efficacy of AKP could be due to the presence of milk solids. These milk solids may act as adjuvants to T. arjuna's phytoconstituents, contributing to their sustained bioavailability, leading to higher in vivo anti-inflammatory efficacy at lower drug concentrations. Elsevier 2016-12-29 /pmc/articles/PMC5634724/ /pubmed/29034188 http://dx.doi.org/10.1016/j.jtcme.2016.11.006 Text en © 2017 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Dube, Nivedita
Nimgulkar, Chetan
Bharatraj, Dinesh Kumar
Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna
title Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna
title_full Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna
title_fullStr Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna
title_full_unstemmed Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna
title_short Validation of therapeutic anti-inflammatory potential of Arjuna Ksheera Paka – A traditional Ayurvedic formulation of Terminalia arjuna
title_sort validation of therapeutic anti-inflammatory potential of arjuna ksheera paka – a traditional ayurvedic formulation of terminalia arjuna
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634724/
https://www.ncbi.nlm.nih.gov/pubmed/29034188
http://dx.doi.org/10.1016/j.jtcme.2016.11.006
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