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Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function
BACKGROUND: This experiment was performed to determine the effect of polyphenolic (-)-epigallocatechin (EGCG), the most abundant catechin of green tea, given at reperfusion period. METHODS: Isolated rat hearts were subjected to 30 min of regional ischemia and 2 h of reperfusion. Green tea extract (G...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Society of Anesthesiologists
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872859/ https://www.ncbi.nlm.nih.gov/pubmed/20498796 http://dx.doi.org/10.4097/kjae.2010.58.2.169 |
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author | Kim, Chan Jin Kim, Jin Mo Lee, Seung Ryong Jang, Young Ho Kim, June Hong Chun, Kook Jin |
author_facet | Kim, Chan Jin Kim, Jin Mo Lee, Seung Ryong Jang, Young Ho Kim, June Hong Chun, Kook Jin |
author_sort | Kim, Chan Jin |
collection | PubMed |
description | BACKGROUND: This experiment was performed to determine the effect of polyphenolic (-)-epigallocatechin (EGCG), the most abundant catechin of green tea, given at reperfusion period. METHODS: Isolated rat hearts were subjected to 30 min of regional ischemia and 2 h of reperfusion. Green tea extract (GT) was perfused with the following concentrations; 0, 0.5, and 1 µM (GT-O, GT-0.5, and GT-1, respectively). In a next experiment, hearts were assigned randomly to one of the following groups; Control, EGCG-1 (1 µM of EGCG), and EGCG-10 (10 µM of EGCG). GT and EGCG were perfused for a period of 5 min before and 30 min after reperfusion. For comparison of cardioprotection among groups, morphometric measurement was performed by 2,3,5-triphenyltetrazolium chloride staning. RESULTS: GT 1 µM (10.3 ± 2.1%, P < 0.05) significantly reduced infarct volume as a percentage of ischemic volume compared to untreated hearts (27.4 ± 1.1%). EGCG 10 µM (13.2 ± 4.0%) significantly reduced myocardial infarction compared to control hearts (27.2 ± 1.4%, P = 0.002). After 2 h of reperfusion, cardiodynamic variables, including left ventricular developed pressure, rate-pressure produce, +dP/dt(max), and -dP/dt(min) were significantly improved by 10 µM of EGCG compared to control hearts (P = 0.01, 0.016, 0.009, and 0.019, respectively). CONCLUSIONS: EGCG treatment at an early reperfusion period reduces myocardial infarction and improves cardiodynamics in isolated rat hearts. |
format | Text |
id | pubmed-2872859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Korean Society of Anesthesiologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-28728592010-05-24 Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function Kim, Chan Jin Kim, Jin Mo Lee, Seung Ryong Jang, Young Ho Kim, June Hong Chun, Kook Jin Korean J Anesthesiol Experimental Research Article BACKGROUND: This experiment was performed to determine the effect of polyphenolic (-)-epigallocatechin (EGCG), the most abundant catechin of green tea, given at reperfusion period. METHODS: Isolated rat hearts were subjected to 30 min of regional ischemia and 2 h of reperfusion. Green tea extract (GT) was perfused with the following concentrations; 0, 0.5, and 1 µM (GT-O, GT-0.5, and GT-1, respectively). In a next experiment, hearts were assigned randomly to one of the following groups; Control, EGCG-1 (1 µM of EGCG), and EGCG-10 (10 µM of EGCG). GT and EGCG were perfused for a period of 5 min before and 30 min after reperfusion. For comparison of cardioprotection among groups, morphometric measurement was performed by 2,3,5-triphenyltetrazolium chloride staning. RESULTS: GT 1 µM (10.3 ± 2.1%, P < 0.05) significantly reduced infarct volume as a percentage of ischemic volume compared to untreated hearts (27.4 ± 1.1%). EGCG 10 µM (13.2 ± 4.0%) significantly reduced myocardial infarction compared to control hearts (27.2 ± 1.4%, P = 0.002). After 2 h of reperfusion, cardiodynamic variables, including left ventricular developed pressure, rate-pressure produce, +dP/dt(max), and -dP/dt(min) were significantly improved by 10 µM of EGCG compared to control hearts (P = 0.01, 0.016, 0.009, and 0.019, respectively). CONCLUSIONS: EGCG treatment at an early reperfusion period reduces myocardial infarction and improves cardiodynamics in isolated rat hearts. The Korean Society of Anesthesiologists 2010-02 2010-02-28 /pmc/articles/PMC2872859/ /pubmed/20498796 http://dx.doi.org/10.4097/kjae.2010.58.2.169 Text en Copyright © The Korean Society of Anesthesiologists, 2010 http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Experimental Research Article Kim, Chan Jin Kim, Jin Mo Lee, Seung Ryong Jang, Young Ho Kim, June Hong Chun, Kook Jin Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
title | Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
title_full | Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
title_fullStr | Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
title_full_unstemmed | Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
title_short | Polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
title_sort | polyphenol (-)-epigallocatechin gallate targeting myocardial reperfusion limits infarct size and improves cardiac function |
topic | Experimental Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872859/ https://www.ncbi.nlm.nih.gov/pubmed/20498796 http://dx.doi.org/10.4097/kjae.2010.58.2.169 |
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