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Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats
INTRODUCTION: Resveratrol is a natural polyphenol present mainly in grapes. It has been shown to offer strong cardio protection in animal models due to its ability to correct lipid peroxidation and maintain antioxidants level. Atorvastatin, a HMG-CoA reductase inhibitor, lowers cholesterol level and...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517328/ https://www.ncbi.nlm.nih.gov/pubmed/26229360 http://dx.doi.org/10.4103/0975-7406.160037 |
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author | Chakraborty, Songjukta Pujani, Mukta Haque, Syed Ehtaishamul |
author_facet | Chakraborty, Songjukta Pujani, Mukta Haque, Syed Ehtaishamul |
author_sort | Chakraborty, Songjukta |
collection | PubMed |
description | INTRODUCTION: Resveratrol is a natural polyphenol present mainly in grapes. It has been shown to offer strong cardio protection in animal models due to its ability to correct lipid peroxidation and maintain antioxidants level. Atorvastatin, a HMG-CoA reductase inhibitor, lowers cholesterol level and is commonly prescribed to heart patients. Our aim in this study was to see the combination effect of these two drugs against Isoproterenol-induced cardiac hypertrophy in rats. MATERIALS AND METHODS: Wister Albino rats were treated with resveratrol (20 mg/kg/day, p.o), atorvastatin (20 mg/kg/day, p.o) and in combination (resveratrol [10 mg/kg/day, p.o] + atorvastatin [10 mg/kg/day, p.o]) for a period of 25 days and from 15(th) till 25(th) day Isoproterenol (5 mg/kg/day, s.c) was co-administered to rats to induce cardiac hypertrophy. RESULTS: A significant increase in creatine kinase, lactate dehydrogenase, aspartate transaminase and lipid peroxidation with the significant decrease in reduced glutathione, superoxide dismutase and catalase were observed in Isoproterenol treated rats. Resveratrol, atorvastatin and their combination significantly reversed the effect. The histopathological studies and myocardial infarct size evaluation also confirmed the protection. CONCLUSION: Comparing the data we came to this conclusion that atorvastatin although showed the protection along all the parameters, the extent of protection offered by resveratrol alone and in combination were more effective. Hence, it can be concluded that resveratrol, an herbal nutritional supplement, alone and in combination is better against cardiac hypertrophy. |
format | Online Article Text |
id | pubmed-4517328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45173282015-07-30 Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats Chakraborty, Songjukta Pujani, Mukta Haque, Syed Ehtaishamul J Pharm Bioallied Sci Original Article INTRODUCTION: Resveratrol is a natural polyphenol present mainly in grapes. It has been shown to offer strong cardio protection in animal models due to its ability to correct lipid peroxidation and maintain antioxidants level. Atorvastatin, a HMG-CoA reductase inhibitor, lowers cholesterol level and is commonly prescribed to heart patients. Our aim in this study was to see the combination effect of these two drugs against Isoproterenol-induced cardiac hypertrophy in rats. MATERIALS AND METHODS: Wister Albino rats were treated with resveratrol (20 mg/kg/day, p.o), atorvastatin (20 mg/kg/day, p.o) and in combination (resveratrol [10 mg/kg/day, p.o] + atorvastatin [10 mg/kg/day, p.o]) for a period of 25 days and from 15(th) till 25(th) day Isoproterenol (5 mg/kg/day, s.c) was co-administered to rats to induce cardiac hypertrophy. RESULTS: A significant increase in creatine kinase, lactate dehydrogenase, aspartate transaminase and lipid peroxidation with the significant decrease in reduced glutathione, superoxide dismutase and catalase were observed in Isoproterenol treated rats. Resveratrol, atorvastatin and their combination significantly reversed the effect. The histopathological studies and myocardial infarct size evaluation also confirmed the protection. CONCLUSION: Comparing the data we came to this conclusion that atorvastatin although showed the protection along all the parameters, the extent of protection offered by resveratrol alone and in combination were more effective. Hence, it can be concluded that resveratrol, an herbal nutritional supplement, alone and in combination is better against cardiac hypertrophy. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4517328/ /pubmed/26229360 http://dx.doi.org/10.4103/0975-7406.160037 Text en Copyright: © 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-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 Chakraborty, Songjukta Pujani, Mukta Haque, Syed Ehtaishamul Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
title | Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
title_full | Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
title_fullStr | Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
title_full_unstemmed | Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
title_short | Combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
title_sort | combinational effect of resveratrol and atorvastatin on isoproterenol-induced cardiac hypertrophy in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517328/ https://www.ncbi.nlm.nih.gov/pubmed/26229360 http://dx.doi.org/10.4103/0975-7406.160037 |
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