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Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction
Cardioprotective potential of anthocyanin rich red cabbage extract (ARCE) was assessed in H(2)O(2) treated rat neonatal cardiomyoblasts (H9c2 cells) and isoproterenol (ISO) induced rodent model of myocardial infarction. H(2)O(2) treated H9c2 cells recorded cytotoxicity (48–50%) and apoptosis (57.3%)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538674/ https://www.ncbi.nlm.nih.gov/pubmed/28763488 http://dx.doi.org/10.1371/journal.pone.0182137 |
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author | Jana, Sarmita Patel, Dipak Patel, Shweta Upadhyay, Kapil Thadani, Jaymesh Mandal, Rahul Das, Santasabuj Devkar, Ranjitsinh |
author_facet | Jana, Sarmita Patel, Dipak Patel, Shweta Upadhyay, Kapil Thadani, Jaymesh Mandal, Rahul Das, Santasabuj Devkar, Ranjitsinh |
author_sort | Jana, Sarmita |
collection | PubMed |
description | Cardioprotective potential of anthocyanin rich red cabbage extract (ARCE) was assessed in H(2)O(2) treated rat neonatal cardiomyoblasts (H9c2 cells) and isoproterenol (ISO) induced rodent model of myocardial infarction. H(2)O(2) treated H9c2 cells recorded cytotoxicity (48–50%) and apoptosis (57.3%), the same were reduced in presence of ARCE (7–10% & 12.3% respectively). Rats pretreated with ARCE for 30 days followed by ISO treatment recorded favourable heart: body weight ratio as compared to ISO treated group. Also, the mRNA levels of enzymatic antioxidants (sod and catalase) and apoptotic genes (bax and bcl-2) in ARCE+ISO treated group were similar to the control group suggesting that ARCE pretreatment prevents ISO induced depletion of enzymatic antioxidants and apoptosis. Histoarchitecture of ventricular tissue of ISO treated group was marked by infracted areas (10%) and derangement of myocardium whereas, ARCE+ISO treated group (4.5%) recorded results comparable to control (0%). ARCE+ISO treated group accounted for upregulation of caveolin-3 and SERCA2a expression as compared to the ISO treated group implying towards ARCE mediated reduction in membrane damage and calcium imbalance. Molecular docking scores and LigPlot analysis of cyanidin-3-glucoside (-8.7 Kcal/mol) and delphinidin-3-glucoside (-8.5 Kcal/mol) showed stable hydrophobic and electrostatic interactions with β(1) adrenergic receptor. Overall this study elucidates the mechanism of ARCE mediated prevention of experimentally induced myocardial damage. |
format | Online Article Text |
id | pubmed-5538674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55386742017-08-07 Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction Jana, Sarmita Patel, Dipak Patel, Shweta Upadhyay, Kapil Thadani, Jaymesh Mandal, Rahul Das, Santasabuj Devkar, Ranjitsinh PLoS One Research Article Cardioprotective potential of anthocyanin rich red cabbage extract (ARCE) was assessed in H(2)O(2) treated rat neonatal cardiomyoblasts (H9c2 cells) and isoproterenol (ISO) induced rodent model of myocardial infarction. H(2)O(2) treated H9c2 cells recorded cytotoxicity (48–50%) and apoptosis (57.3%), the same were reduced in presence of ARCE (7–10% & 12.3% respectively). Rats pretreated with ARCE for 30 days followed by ISO treatment recorded favourable heart: body weight ratio as compared to ISO treated group. Also, the mRNA levels of enzymatic antioxidants (sod and catalase) and apoptotic genes (bax and bcl-2) in ARCE+ISO treated group were similar to the control group suggesting that ARCE pretreatment prevents ISO induced depletion of enzymatic antioxidants and apoptosis. Histoarchitecture of ventricular tissue of ISO treated group was marked by infracted areas (10%) and derangement of myocardium whereas, ARCE+ISO treated group (4.5%) recorded results comparable to control (0%). ARCE+ISO treated group accounted for upregulation of caveolin-3 and SERCA2a expression as compared to the ISO treated group implying towards ARCE mediated reduction in membrane damage and calcium imbalance. Molecular docking scores and LigPlot analysis of cyanidin-3-glucoside (-8.7 Kcal/mol) and delphinidin-3-glucoside (-8.5 Kcal/mol) showed stable hydrophobic and electrostatic interactions with β(1) adrenergic receptor. Overall this study elucidates the mechanism of ARCE mediated prevention of experimentally induced myocardial damage. Public Library of Science 2017-08-01 /pmc/articles/PMC5538674/ /pubmed/28763488 http://dx.doi.org/10.1371/journal.pone.0182137 Text en © 2017 Jana et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jana, Sarmita Patel, Dipak Patel, Shweta Upadhyay, Kapil Thadani, Jaymesh Mandal, Rahul Das, Santasabuj Devkar, Ranjitsinh Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction |
title | Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction |
title_full | Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction |
title_fullStr | Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction |
title_full_unstemmed | Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction |
title_short | Anthocyanin rich extract of Brassica oleracea L. alleviates experimentally induced myocardial infarction |
title_sort | anthocyanin rich extract of brassica oleracea l. alleviates experimentally induced myocardial infarction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538674/ https://www.ncbi.nlm.nih.gov/pubmed/28763488 http://dx.doi.org/10.1371/journal.pone.0182137 |
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