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An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract

BACKGROUND: Stress is a normal part of everyday life but chronic stress can lead to a variety of stress-related illnesses including hypertension, anxiety, and depression. In the present investigation, standardized leaf extract of Epipremnumaureum was evaluated for its anti-stress potential. MATERIAL...

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Autores principales: Das, Sreemoy Kanti, Sengupta, Pinaki, Mustapha, Mohd. Shahimi, Sarker, Md. Moklesur Rahman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508421/
https://www.ncbi.nlm.nih.gov/pubmed/28717330
http://dx.doi.org/10.4103/0975-7406.183227
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author Das, Sreemoy Kanti
Sengupta, Pinaki
Mustapha, Mohd. Shahimi
Sarker, Md. Moklesur Rahman
author_facet Das, Sreemoy Kanti
Sengupta, Pinaki
Mustapha, Mohd. Shahimi
Sarker, Md. Moklesur Rahman
author_sort Das, Sreemoy Kanti
collection PubMed
description BACKGROUND: Stress is a normal part of everyday life but chronic stress can lead to a variety of stress-related illnesses including hypertension, anxiety, and depression. In the present investigation, standardized leaf extract of Epipremnumaureum was evaluated for its anti-stress potential. MATERIALS AND METHODS: For the evaluation of anti-stress activity, groups of mice (n = 6) were subjected to forced swim stress and anoxic stress tolerance test in mice 1h after daily treatment of E.aureumextract. Diazepam (5 mg/kg) was taken as a reference standard. Urinary vanillylmandelic acid (VMA) and ascorbic acid were selected as noninvasive biomarkers to assess the anti-stress activity and plasma cortisol, blood ascorbic acid, and weight of adrenal were measured. The 24 h urinary excretion of VMA and ascorbic acid were determined by spectrophotometric methods in all groups under normal and stressed conditions. The hematological parameters (neutrophils, lymphocytes, and eosinophils) were also determined. RESULTS: Administration of E.aureumat doses of 400 and 600 mg/kg wasfound to be effective in inhibiting the stress induced urinary biochemical changes in a dose-dependent manner. Treatment with E. aureum extract prevents the rise in blood ascorbic acid and plasma cortisol. Moreover, the extract prevented the increase in weight of adrenal gland also significantly increased the anoxia stress tolerance time. Dose-dependent significant reduction in white blood cell count was observed in anoxic stress tolerance test as compared to stressed group. CONCLUSION: Hence, the present study provides scientific support for the positiveadaptogenic effect of E. aureum extract.
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spelling pubmed-55084212017-07-17 An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract Das, Sreemoy Kanti Sengupta, Pinaki Mustapha, Mohd. Shahimi Sarker, Md. Moklesur Rahman J Pharm Bioallied Sci Original Article BACKGROUND: Stress is a normal part of everyday life but chronic stress can lead to a variety of stress-related illnesses including hypertension, anxiety, and depression. In the present investigation, standardized leaf extract of Epipremnumaureum was evaluated for its anti-stress potential. MATERIALS AND METHODS: For the evaluation of anti-stress activity, groups of mice (n = 6) were subjected to forced swim stress and anoxic stress tolerance test in mice 1h after daily treatment of E.aureumextract. Diazepam (5 mg/kg) was taken as a reference standard. Urinary vanillylmandelic acid (VMA) and ascorbic acid were selected as noninvasive biomarkers to assess the anti-stress activity and plasma cortisol, blood ascorbic acid, and weight of adrenal were measured. The 24 h urinary excretion of VMA and ascorbic acid were determined by spectrophotometric methods in all groups under normal and stressed conditions. The hematological parameters (neutrophils, lymphocytes, and eosinophils) were also determined. RESULTS: Administration of E.aureumat doses of 400 and 600 mg/kg wasfound to be effective in inhibiting the stress induced urinary biochemical changes in a dose-dependent manner. Treatment with E. aureum extract prevents the rise in blood ascorbic acid and plasma cortisol. Moreover, the extract prevented the increase in weight of adrenal gland also significantly increased the anoxia stress tolerance time. Dose-dependent significant reduction in white blood cell count was observed in anoxic stress tolerance test as compared to stressed group. CONCLUSION: Hence, the present study provides scientific support for the positiveadaptogenic effect of E. aureum extract. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5508421/ /pubmed/28717330 http://dx.doi.org/10.4103/0975-7406.183227 Text en Copyright: © 2017 Journal of Pharmacy and Bioallied Sciences 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 Original Article
Das, Sreemoy Kanti
Sengupta, Pinaki
Mustapha, Mohd. Shahimi
Sarker, Md. Moklesur Rahman
An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract
title An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract
title_full An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract
title_fullStr An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract
title_full_unstemmed An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract
title_short An Experimental Evaluation of Adaptogenic Potential of Standardized Epipremnum Aureum Leaf Extract
title_sort experimental evaluation of adaptogenic potential of standardized epipremnum aureum leaf extract
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508421/
https://www.ncbi.nlm.nih.gov/pubmed/28717330
http://dx.doi.org/10.4103/0975-7406.183227
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