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Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model

OBJECTIVE: Obesity plays a central role in the insulin resistance syndrome, which is associated with hyperinsulinemia, hypertension, hyperlipidemia, type 2 diabetes mellitus, and an increased risk of atherosclerotic cardiovascular disease. The present study was done to assess the effect of Gymnema s...

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Autores principales: Kumar, Vinay, Bhandari, Uma, Tripathi, Chakra Dhar, Khanna, Geetika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480794/
https://www.ncbi.nlm.nih.gov/pubmed/23112423
http://dx.doi.org/10.4103/0253-7613.100387
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author Kumar, Vinay
Bhandari, Uma
Tripathi, Chakra Dhar
Khanna, Geetika
author_facet Kumar, Vinay
Bhandari, Uma
Tripathi, Chakra Dhar
Khanna, Geetika
author_sort Kumar, Vinay
collection PubMed
description OBJECTIVE: Obesity plays a central role in the insulin resistance syndrome, which is associated with hyperinsulinemia, hypertension, hyperlipidemia, type 2 diabetes mellitus, and an increased risk of atherosclerotic cardiovascular disease. The present study was done to assess the effect of Gymnema sylvestre extract (GSE) in the high fat diet (HFD)-induced cellular obesity and cardiac damage in Wistar rats. MATERIALS AND METHODS: Adult male Wistar rats (150–200 g body weight) were used in this study. HFD was used to induce obesity. Body mass index, hemodynamic parameters, serum leptin, insulin, glucose, lipids, apolipoprotein levels, myocardial apoptosis, and antioxidant enzymes were assessed. Organ and visceral fat pad weights and histopathological studies were also carried out. RESULTS: Oral feeding of HFD (20 g/day) for a period of 28 days resulted in a significant increase in body mass index, organ weights, visceral fat pad weight, cardiac caspase-3, cardiac DNA laddering (indicating apoptotic inter-nucleosomal DNA fragment), and lipid peroxide levels of cardiac tissues of rats. Further, mean arterial blood pressure, heart rate, serum leptin, insulin, LDH, LDL-C, total cholesterol, triglycerides, and apolipoprotein-B levels were enhanced significantly, whereas serum HDL-C, apoliporotein-A1 levels, and cardiac Na(+) K(+) ATPase, antioxidant enzymes levels were significantly decreased. Furthermore, treatment with standardized ethanolic GSE (200 m/kg/p.o.) for a period of 28 days resulted in significant reversal of above mentioned changes in the obese Wistar rats. CONCLUSION: The present study has demonstrated the significant antiobesity potential of GSE in murine model of obesity.
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spelling pubmed-34807942012-10-30 Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model Kumar, Vinay Bhandari, Uma Tripathi, Chakra Dhar Khanna, Geetika Indian J Pharmacol Research Article OBJECTIVE: Obesity plays a central role in the insulin resistance syndrome, which is associated with hyperinsulinemia, hypertension, hyperlipidemia, type 2 diabetes mellitus, and an increased risk of atherosclerotic cardiovascular disease. The present study was done to assess the effect of Gymnema sylvestre extract (GSE) in the high fat diet (HFD)-induced cellular obesity and cardiac damage in Wistar rats. MATERIALS AND METHODS: Adult male Wistar rats (150–200 g body weight) were used in this study. HFD was used to induce obesity. Body mass index, hemodynamic parameters, serum leptin, insulin, glucose, lipids, apolipoprotein levels, myocardial apoptosis, and antioxidant enzymes were assessed. Organ and visceral fat pad weights and histopathological studies were also carried out. RESULTS: Oral feeding of HFD (20 g/day) for a period of 28 days resulted in a significant increase in body mass index, organ weights, visceral fat pad weight, cardiac caspase-3, cardiac DNA laddering (indicating apoptotic inter-nucleosomal DNA fragment), and lipid peroxide levels of cardiac tissues of rats. Further, mean arterial blood pressure, heart rate, serum leptin, insulin, LDH, LDL-C, total cholesterol, triglycerides, and apolipoprotein-B levels were enhanced significantly, whereas serum HDL-C, apoliporotein-A1 levels, and cardiac Na(+) K(+) ATPase, antioxidant enzymes levels were significantly decreased. Furthermore, treatment with standardized ethanolic GSE (200 m/kg/p.o.) for a period of 28 days resulted in significant reversal of above mentioned changes in the obese Wistar rats. CONCLUSION: The present study has demonstrated the significant antiobesity potential of GSE in murine model of obesity. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3480794/ /pubmed/23112423 http://dx.doi.org/10.4103/0253-7613.100387 Text en Copyright: © Indian Journal of Pharmacology 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 Research Article
Kumar, Vinay
Bhandari, Uma
Tripathi, Chakra Dhar
Khanna, Geetika
Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model
title Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model
title_full Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model
title_fullStr Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model
title_full_unstemmed Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model
title_short Evaluation of antiobesity and cardioprotective effect of Gymnema sylvestre extract in murine model
title_sort evaluation of antiobesity and cardioprotective effect of gymnema sylvestre extract in murine model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480794/
https://www.ncbi.nlm.nih.gov/pubmed/23112423
http://dx.doi.org/10.4103/0253-7613.100387
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