A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection

Abstract To develop a reproducible and stable closed chest model of ischemic cardiogenic shock in sheep, with high survival rate and potential insight into human pathology. We established a protocol for multi-step myocardial alcoholisation of the left anterior descending coronary artery by percutane...

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Autores principales: Mario Rienzo, Julien Imbault, Younes El Boustani, Antoine Beurton, Carolina Carlos Sampedrano, Philippe Pasdois, Mathieu Pernot, Olivier Bernus, Michel Haïssaguerre, Thierry Couffinhal, Alexandre Ouattara
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Publicado: Nature Portfolio 2020
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spelling oai:doaj.org-article:a9ab62cd62b94e569590e9cc481308fc2021-12-02T16:26:21ZA total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection10.1038/s41598-020-68571-52045-2322https://doaj.org/article/a9ab62cd62b94e569590e9cc481308fc2020-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-68571-5https://doaj.org/toc/2045-2322Abstract To develop a reproducible and stable closed chest model of ischemic cardiogenic shock in sheep, with high survival rate and potential insight into human pathology. We established a protocol for multi-step myocardial alcoholisation of the left anterior descending coronary artery by percutaneous ethanol injection. A thorough hemodynamic assessment was obtained by invasive and non-invasive monitoring devices. Repeated blood samples were obtained to determine haemoglobin and alcohol concentration, electrolytes, blood gas parameters and cardiac troponin I. After sacrifice, tissue was excised for quantification of infarction and histology. Cardiogenic shock was characterized by a significant decrease in mean arterial pressure (− 33%), cardiac output (− 29%), dP/dt max (− 28%), carotid blood flow (− 22%), left ventricular fractional shortening (− 28%), and left ventricle end-systolic pressure–volume relationship (− 51%). Lactate and cardiac troponin I levels increased from 1.4 ± 0.2 to 4.9 ± 0.7 mmol/L (p = 0.001) and from 0.05 ± 0.02 to 14.74 ± 2.59 µg/L (p = 0.001), respectively. All haemodynamic changes were stable over a three-hour period with a 71% survival rate. The necrotic volume (n = 5) represented 24.0 ± 1.9% of total ventricular mass. No sham exhibited any variation under general anaesthesia. We described and characterized, for the first time, a stable, reproducible sheep model of cardiogenic shock obtained by percutaneous intracoronary ethanol administration.Mario RienzoJulien ImbaultYounes El BoustaniAntoine BeurtonCarolina Carlos SampedranoPhilippe PasdoisMathieu PernotOlivier BernusMichel HaïssaguerreThierry CouffinhalAlexandre OuattaraNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Mario Rienzo
Julien Imbault
Younes El Boustani
Antoine Beurton
Carolina Carlos Sampedrano
Philippe Pasdois
Mathieu Pernot
Olivier Bernus
Michel Haïssaguerre
Thierry Couffinhal
Alexandre Ouattara
A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
description Abstract To develop a reproducible and stable closed chest model of ischemic cardiogenic shock in sheep, with high survival rate and potential insight into human pathology. We established a protocol for multi-step myocardial alcoholisation of the left anterior descending coronary artery by percutaneous ethanol injection. A thorough hemodynamic assessment was obtained by invasive and non-invasive monitoring devices. Repeated blood samples were obtained to determine haemoglobin and alcohol concentration, electrolytes, blood gas parameters and cardiac troponin I. After sacrifice, tissue was excised for quantification of infarction and histology. Cardiogenic shock was characterized by a significant decrease in mean arterial pressure (− 33%), cardiac output (− 29%), dP/dt max (− 28%), carotid blood flow (− 22%), left ventricular fractional shortening (− 28%), and left ventricle end-systolic pressure–volume relationship (− 51%). Lactate and cardiac troponin I levels increased from 1.4 ± 0.2 to 4.9 ± 0.7 mmol/L (p = 0.001) and from 0.05 ± 0.02 to 14.74 ± 2.59 µg/L (p = 0.001), respectively. All haemodynamic changes were stable over a three-hour period with a 71% survival rate. The necrotic volume (n = 5) represented 24.0 ± 1.9% of total ventricular mass. No sham exhibited any variation under general anaesthesia. We described and characterized, for the first time, a stable, reproducible sheep model of cardiogenic shock obtained by percutaneous intracoronary ethanol administration.
format article
author Mario Rienzo
Julien Imbault
Younes El Boustani
Antoine Beurton
Carolina Carlos Sampedrano
Philippe Pasdois
Mathieu Pernot
Olivier Bernus
Michel Haïssaguerre
Thierry Couffinhal
Alexandre Ouattara
author_facet Mario Rienzo
Julien Imbault
Younes El Boustani
Antoine Beurton
Carolina Carlos Sampedrano
Philippe Pasdois
Mathieu Pernot
Olivier Bernus
Michel Haïssaguerre
Thierry Couffinhal
Alexandre Ouattara
author_sort Mario Rienzo
title A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
title_short A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
title_full A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
title_fullStr A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
title_full_unstemmed A total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
title_sort total closed chest sheep model of cardiogenic shock by percutaneous intracoronary ethanol injection
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/a9ab62cd62b94e569590e9cc481308fc
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