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Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model
Consumption of flavonoid-rich nutraceuticals has been associated with a reduction in coronary events. The present study analyzed the effects of cocoa flavonols on myocardial injury following acute coronary ischemia-reperfusion (I/R). A commercially available cocoa extract was identified by chromatog...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070606/ https://www.ncbi.nlm.nih.gov/pubmed/32085604 http://dx.doi.org/10.3390/antiox9020167 |
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author | Ahmed, Sajeela Ahmed, Naseer Rungatscher, Alessio Linardi, Daniele Kulsoom, Bibi Innamorati, Giulio Meo, Sultan Ayoub Gebrie, Mebratu Alebachew Mani, Romel Merigo, Flavia Guzzo, Flavia Faggian, Giuseppe |
author_facet | Ahmed, Sajeela Ahmed, Naseer Rungatscher, Alessio Linardi, Daniele Kulsoom, Bibi Innamorati, Giulio Meo, Sultan Ayoub Gebrie, Mebratu Alebachew Mani, Romel Merigo, Flavia Guzzo, Flavia Faggian, Giuseppe |
author_sort | Ahmed, Sajeela |
collection | PubMed |
description | Consumption of flavonoid-rich nutraceuticals has been associated with a reduction in coronary events. The present study analyzed the effects of cocoa flavonols on myocardial injury following acute coronary ischemia-reperfusion (I/R). A commercially available cocoa extract was identified by chromatographic mass spectrometry. Nineteen different phenolic compounds were identified and 250 mg of flavan-3-ols (procyanidin) were isolated in 1 g of extract. Oral administration of cocoa extract in incremental doses from 5 mg/kg up to 25 mg/kg daily for 15 days in Sprague Dawley rats (n = 30) produced a corresponding increase of blood serum polyphenols and become constant after 15 mg/kg. Consequently, the selected dose (15 mg/kg) of cocoa extract was administered orally daily for 15 days in a treated group (n = 10) and an untreated group served as control (n = 10). Both groups underwent surgical occlusion of the left anterior descending coronary artery and reperfusion. Cocoa extract treatment significantly reversed membrane peroxidation, nitro-oxidative stress, and decreased inflammatory markers (IL-6 and NF-kB) caused by myocardial I/R injury and enhanced activation of both p-Akt and p-Erk1/2. Daily administration of cocoa extract in rats is protective against myocardial I/R injury and attenuate nitro-oxidative stress, inflammation, and mitigates myocardial apoptosis. |
format | Online Article Text |
id | pubmed-7070606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70706062020-03-19 Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model Ahmed, Sajeela Ahmed, Naseer Rungatscher, Alessio Linardi, Daniele Kulsoom, Bibi Innamorati, Giulio Meo, Sultan Ayoub Gebrie, Mebratu Alebachew Mani, Romel Merigo, Flavia Guzzo, Flavia Faggian, Giuseppe Antioxidants (Basel) Article Consumption of flavonoid-rich nutraceuticals has been associated with a reduction in coronary events. The present study analyzed the effects of cocoa flavonols on myocardial injury following acute coronary ischemia-reperfusion (I/R). A commercially available cocoa extract was identified by chromatographic mass spectrometry. Nineteen different phenolic compounds were identified and 250 mg of flavan-3-ols (procyanidin) were isolated in 1 g of extract. Oral administration of cocoa extract in incremental doses from 5 mg/kg up to 25 mg/kg daily for 15 days in Sprague Dawley rats (n = 30) produced a corresponding increase of blood serum polyphenols and become constant after 15 mg/kg. Consequently, the selected dose (15 mg/kg) of cocoa extract was administered orally daily for 15 days in a treated group (n = 10) and an untreated group served as control (n = 10). Both groups underwent surgical occlusion of the left anterior descending coronary artery and reperfusion. Cocoa extract treatment significantly reversed membrane peroxidation, nitro-oxidative stress, and decreased inflammatory markers (IL-6 and NF-kB) caused by myocardial I/R injury and enhanced activation of both p-Akt and p-Erk1/2. Daily administration of cocoa extract in rats is protective against myocardial I/R injury and attenuate nitro-oxidative stress, inflammation, and mitigates myocardial apoptosis. MDPI 2020-02-18 /pmc/articles/PMC7070606/ /pubmed/32085604 http://dx.doi.org/10.3390/antiox9020167 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ahmed, Sajeela Ahmed, Naseer Rungatscher, Alessio Linardi, Daniele Kulsoom, Bibi Innamorati, Giulio Meo, Sultan Ayoub Gebrie, Mebratu Alebachew Mani, Romel Merigo, Flavia Guzzo, Flavia Faggian, Giuseppe Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model |
title | Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model |
title_full | Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model |
title_fullStr | Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model |
title_full_unstemmed | Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model |
title_short | Cocoa Flavonoids Reduce Inflammation and Oxidative Stress in a Myocardial Ischemia-Reperfusion Experimental Model |
title_sort | cocoa flavonoids reduce inflammation and oxidative stress in a myocardial ischemia-reperfusion experimental model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070606/ https://www.ncbi.nlm.nih.gov/pubmed/32085604 http://dx.doi.org/10.3390/antiox9020167 |
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