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Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats
Cardamom is a popular spice that has been commonly used in cuisines for flavor since ancient times. It has copious health benefits such as improving digestion, stimulating metabolism, and exhibits antioxidant and anti-inflammatory effects. The current study investigated the effect of cardamom on hem...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661898/ https://www.ncbi.nlm.nih.gov/pubmed/26593900 http://dx.doi.org/10.3390/ijms161126040 |
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author | Goyal, Sameer N. Sharma, Charu Mahajan, Umesh B. Patil, Chandragouda R. Agrawal, Yogeeta O. Kumari, Santosh Arya, Dharamvir Singh Ojha, Shreesh |
author_facet | Goyal, Sameer N. Sharma, Charu Mahajan, Umesh B. Patil, Chandragouda R. Agrawal, Yogeeta O. Kumari, Santosh Arya, Dharamvir Singh Ojha, Shreesh |
author_sort | Goyal, Sameer N. |
collection | PubMed |
description | Cardamom is a popular spice that has been commonly used in cuisines for flavor since ancient times. It has copious health benefits such as improving digestion, stimulating metabolism, and exhibits antioxidant and anti-inflammatory effects. The current study investigated the effect of cardamom on hemodynamic, biochemical, histopathological and ultrastructural changes in isoproterenol (ISO)-induced myocardial infarction. Wistar male albino rats were randomly divided and treated with extract of cardamom (100 and 200 mg/kg per oral) or normal saline for 30 days with concomitant administration of ISO (85 mg/kg, subcutaneous) on 29th and 30th days, at 24 h interval. ISO injections to rats caused cardiac dysfunction evidenced by declined arterial pressure indices, heart rate, contractility and relaxation along with increased preload. ISO also caused a significant decrease in endogenous antioxidants, superoxide dismutase, catalase, glutathione peroxidase, depletion of cardiomyocytes enzymes, creatine kinase-MB, lactate dehydrogenase and increase in lipid peroxidation. All these changes in cardiac and left ventricular function as well as endogenous antioxidants, lipid peroxidation and myocyte enzymes were ameliorated when the rats were pretreated with cardamom. Additionally, the protective effects were strengthened by improved histopathology and ultrastructural changes, which specifies the salvage of cardiomyocytes from the deleterious effects of ISO. The present study findings demonstrate that cardamom significantly protects the myocardium and exerts cardioprotective effects by free radical scavenging and antioxidant activities. |
format | Online Article Text |
id | pubmed-4661898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-46618982015-12-10 Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats Goyal, Sameer N. Sharma, Charu Mahajan, Umesh B. Patil, Chandragouda R. Agrawal, Yogeeta O. Kumari, Santosh Arya, Dharamvir Singh Ojha, Shreesh Int J Mol Sci Article Cardamom is a popular spice that has been commonly used in cuisines for flavor since ancient times. It has copious health benefits such as improving digestion, stimulating metabolism, and exhibits antioxidant and anti-inflammatory effects. The current study investigated the effect of cardamom on hemodynamic, biochemical, histopathological and ultrastructural changes in isoproterenol (ISO)-induced myocardial infarction. Wistar male albino rats were randomly divided and treated with extract of cardamom (100 and 200 mg/kg per oral) or normal saline for 30 days with concomitant administration of ISO (85 mg/kg, subcutaneous) on 29th and 30th days, at 24 h interval. ISO injections to rats caused cardiac dysfunction evidenced by declined arterial pressure indices, heart rate, contractility and relaxation along with increased preload. ISO also caused a significant decrease in endogenous antioxidants, superoxide dismutase, catalase, glutathione peroxidase, depletion of cardiomyocytes enzymes, creatine kinase-MB, lactate dehydrogenase and increase in lipid peroxidation. All these changes in cardiac and left ventricular function as well as endogenous antioxidants, lipid peroxidation and myocyte enzymes were ameliorated when the rats were pretreated with cardamom. Additionally, the protective effects were strengthened by improved histopathology and ultrastructural changes, which specifies the salvage of cardiomyocytes from the deleterious effects of ISO. The present study findings demonstrate that cardamom significantly protects the myocardium and exerts cardioprotective effects by free radical scavenging and antioxidant activities. MDPI 2015-11-17 /pmc/articles/PMC4661898/ /pubmed/26593900 http://dx.doi.org/10.3390/ijms161126040 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Goyal, Sameer N. Sharma, Charu Mahajan, Umesh B. Patil, Chandragouda R. Agrawal, Yogeeta O. Kumari, Santosh Arya, Dharamvir Singh Ojha, Shreesh Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats |
title | Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats |
title_full | Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats |
title_fullStr | Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats |
title_full_unstemmed | Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats |
title_short | Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats |
title_sort | protective effects of cardamom in isoproterenol-induced myocardial infarction in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661898/ https://www.ncbi.nlm.nih.gov/pubmed/26593900 http://dx.doi.org/10.3390/ijms161126040 |
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