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Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts

BACKGROUND: Silver fir trunk extract (SFTE) is a complex mixture of antioxidative polyphenols (lignans and phenolic acids) from the trunks of silver fir trees (Abies alba, lignum). In our previous study, we have shown that SFTE exerts strong antioxidative and protective effects against atherogenic,...

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Autores principales: Drevenšek, Gorazd, Lunder, Mojca, Benković, Eva Tavčar, Štrukelj, Borut, Kreft, Samo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069298/
https://www.ncbi.nlm.nih.gov/pubmed/27756448
http://dx.doi.org/10.3402/fnr.v60.29623
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author Drevenšek, Gorazd
Lunder, Mojca
Benković, Eva Tavčar
Štrukelj, Borut
Kreft, Samo
author_facet Drevenšek, Gorazd
Lunder, Mojca
Benković, Eva Tavčar
Štrukelj, Borut
Kreft, Samo
author_sort Drevenšek, Gorazd
collection PubMed
description BACKGROUND: Silver fir trunk extract (SFTE) is a complex mixture of antioxidative polyphenols (lignans and phenolic acids) from the trunks of silver fir trees (Abies alba, lignum). In our previous study, we have shown that SFTE exerts strong antioxidative and protective effects against atherogenic, diet-induced arterial wall damage. OBJECTIVE: The aim of the present study was to test the potential protective effects of SFTE and its compounds, two phenolic acids (p-coumaric and protocatechuic acids) in ischemia–reperfusion injury of isolated rat hearts. DESIGN: Isolated hearts of Wistar rats aged 4–8 weeks were exposed to perfusion, ischemia, and reperfusion periods. The experiments were performed using the following five groups: control, SFTE (10 µg/L), SFTE (100 µg/L), protocatechuic acid, and p-coumaric. Aortas were isolated to measure vascular responses in the presence of N(ω)-Nitro-L-arginine. RESULTS: SFTE dose-dependently reduced ischemic-reperfusion heart damage, which was indicated as the decrease in the lactate dehydrogenase (LDH) release rate and arrhythmias duration by 80% and an increase in coronary flow rate during the reperfusion period. Two tested compounds (p-coumaric and protocatechuic acids) acted less cardioprotective, since they decreased the duration of arrhythmias only by 40 and 45%, respectively, and did not decrease LDH release rates during the reperfusion period. Only p-coumaric acid increased coronary flow rates, whereas protocatechuic acid did not. CONCLUSIONS: We conclude that the SFTE exerted the strongest cardioprotective effect, whereas its constituents (the p-coumaric and protocatechuic acids) were less effective in inducing cardioprotection.
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spelling pubmed-50692982016-11-08 Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts Drevenšek, Gorazd Lunder, Mojca Benković, Eva Tavčar Štrukelj, Borut Kreft, Samo Food Nutr Res Original Article BACKGROUND: Silver fir trunk extract (SFTE) is a complex mixture of antioxidative polyphenols (lignans and phenolic acids) from the trunks of silver fir trees (Abies alba, lignum). In our previous study, we have shown that SFTE exerts strong antioxidative and protective effects against atherogenic, diet-induced arterial wall damage. OBJECTIVE: The aim of the present study was to test the potential protective effects of SFTE and its compounds, two phenolic acids (p-coumaric and protocatechuic acids) in ischemia–reperfusion injury of isolated rat hearts. DESIGN: Isolated hearts of Wistar rats aged 4–8 weeks were exposed to perfusion, ischemia, and reperfusion periods. The experiments were performed using the following five groups: control, SFTE (10 µg/L), SFTE (100 µg/L), protocatechuic acid, and p-coumaric. Aortas were isolated to measure vascular responses in the presence of N(ω)-Nitro-L-arginine. RESULTS: SFTE dose-dependently reduced ischemic-reperfusion heart damage, which was indicated as the decrease in the lactate dehydrogenase (LDH) release rate and arrhythmias duration by 80% and an increase in coronary flow rate during the reperfusion period. Two tested compounds (p-coumaric and protocatechuic acids) acted less cardioprotective, since they decreased the duration of arrhythmias only by 40 and 45%, respectively, and did not decrease LDH release rates during the reperfusion period. Only p-coumaric acid increased coronary flow rates, whereas protocatechuic acid did not. CONCLUSIONS: We conclude that the SFTE exerted the strongest cardioprotective effect, whereas its constituents (the p-coumaric and protocatechuic acids) were less effective in inducing cardioprotection. Co-Action Publishing 2016-10-17 /pmc/articles/PMC5069298/ /pubmed/27756448 http://dx.doi.org/10.3402/fnr.v60.29623 Text en © 2016 Gorazd Drevenšek et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
spellingShingle Original Article
Drevenšek, Gorazd
Lunder, Mojca
Benković, Eva Tavčar
Štrukelj, Borut
Kreft, Samo
Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts
title Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts
title_full Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts
title_fullStr Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts
title_full_unstemmed Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts
title_short Cardioprotective effects of silver fir (Abies alba) extract in ischemic-reperfused isolated rat hearts
title_sort cardioprotective effects of silver fir (abies alba) extract in ischemic-reperfused isolated rat hearts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069298/
https://www.ncbi.nlm.nih.gov/pubmed/27756448
http://dx.doi.org/10.3402/fnr.v60.29623
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