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17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study

BACKGROUND: This study was undertaken to compare the in vitro effects of 17β-estradiol on human epicardial coronary arteries, resistance coronary arteries and on arterial vessels usually employed as grafts in surgical myocardial revascularization. METHODS: Coronary artery rings (descending coronary...

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Autores principales: Polvani, Gianluca, Barili, Fabio, Rossoni, Giuseppe, Dainese, Luca, Ossola, Manuela Wally, Topkara, Veli K, Grillo, Francesco, Penza, Eleonora, Tremoli, Elena, Biglioli, Paolo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770916/
https://www.ncbi.nlm.nih.gov/pubmed/17181858
http://dx.doi.org/10.1186/1749-8090-1-46
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author Polvani, Gianluca
Barili, Fabio
Rossoni, Giuseppe
Dainese, Luca
Ossola, Manuela Wally
Topkara, Veli K
Grillo, Francesco
Penza, Eleonora
Tremoli, Elena
Biglioli, Paolo
author_facet Polvani, Gianluca
Barili, Fabio
Rossoni, Giuseppe
Dainese, Luca
Ossola, Manuela Wally
Topkara, Veli K
Grillo, Francesco
Penza, Eleonora
Tremoli, Elena
Biglioli, Paolo
author_sort Polvani, Gianluca
collection PubMed
description BACKGROUND: This study was undertaken to compare the in vitro effects of 17β-estradiol on human epicardial coronary arteries, resistance coronary arteries and on arterial vessels usually employed as grafts in surgical myocardial revascularization. METHODS: Coronary artery rings (descending coronary artery, right coronary artery, circumflex coronary artery, first septal branch) and arterial graft rings (internal thoracic artery, gastro-epiploic artery) obtained from human heart donors with heart not suitable to cardiac transplantation were connected to force transducer for isometric force recording. Precontracted specimens with and without endothelium were exposed to increasing concentration of 17β-estradiol (3–30–300–3000 nmol/l) and to vehicle (0.1% v/v ethanol). We also evaluated the effects of 17β-estradiol on vessels before and 20 minutes after exposure to L-monomethyl-arginine and indomethacin. RESULTS: 17β-estradiol induced a significant relaxation in all precontracted vessels (mean maximum effect: 78,6% ± 8,5). This effect was not different among the different rings and was not related to the presence of endothelium. N-monomethyl-L-arginine and indomethacin did not modify 17β-estradiol relaxant effect. CONCLUSION: The vasodilator action of the 17β-estradiol is similar on coronary arteries, resistance coronary arteries and arterial vessels usually employed as grafts in myocardial revascularization.
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spelling pubmed-17709162007-01-17 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study Polvani, Gianluca Barili, Fabio Rossoni, Giuseppe Dainese, Luca Ossola, Manuela Wally Topkara, Veli K Grillo, Francesco Penza, Eleonora Tremoli, Elena Biglioli, Paolo J Cardiothorac Surg Research Article BACKGROUND: This study was undertaken to compare the in vitro effects of 17β-estradiol on human epicardial coronary arteries, resistance coronary arteries and on arterial vessels usually employed as grafts in surgical myocardial revascularization. METHODS: Coronary artery rings (descending coronary artery, right coronary artery, circumflex coronary artery, first septal branch) and arterial graft rings (internal thoracic artery, gastro-epiploic artery) obtained from human heart donors with heart not suitable to cardiac transplantation were connected to force transducer for isometric force recording. Precontracted specimens with and without endothelium were exposed to increasing concentration of 17β-estradiol (3–30–300–3000 nmol/l) and to vehicle (0.1% v/v ethanol). We also evaluated the effects of 17β-estradiol on vessels before and 20 minutes after exposure to L-monomethyl-arginine and indomethacin. RESULTS: 17β-estradiol induced a significant relaxation in all precontracted vessels (mean maximum effect: 78,6% ± 8,5). This effect was not different among the different rings and was not related to the presence of endothelium. N-monomethyl-L-arginine and indomethacin did not modify 17β-estradiol relaxant effect. CONCLUSION: The vasodilator action of the 17β-estradiol is similar on coronary arteries, resistance coronary arteries and arterial vessels usually employed as grafts in myocardial revascularization. BioMed Central 2006-12-20 /pmc/articles/PMC1770916/ /pubmed/17181858 http://dx.doi.org/10.1186/1749-8090-1-46 Text en Copyright © 2006 Polvani et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Polvani, Gianluca
Barili, Fabio
Rossoni, Giuseppe
Dainese, Luca
Ossola, Manuela Wally
Topkara, Veli K
Grillo, Francesco
Penza, Eleonora
Tremoli, Elena
Biglioli, Paolo
17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
title 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
title_full 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
title_fullStr 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
title_full_unstemmed 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
title_short 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
title_sort 17β-estradiol effects on human coronaries and grafts employed in myocardial revascularization: a preliminary study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770916/
https://www.ncbi.nlm.nih.gov/pubmed/17181858
http://dx.doi.org/10.1186/1749-8090-1-46
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