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An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”

Coronary blood flow adapts to metabolic demand ("metabolic regulation") and remains relatively constant over a range of pressure changes ("autoregulation"). Coronary metabolic regulation and autoregulation are usually studied separately. We developed an intact animal experimental...

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Autores principales: Boudart, Céline, Su, Fuhong, Herpain, Antoine, Creteur, Jacques, Naeije, Robert, Brimioulle, Serge, Dewachter, Laurence, Van Obbergh, Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392130/
https://www.ncbi.nlm.nih.gov/pubmed/32729991
http://dx.doi.org/10.14814/phy2.14510
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author Boudart, Céline
Su, Fuhong
Herpain, Antoine
Creteur, Jacques
Naeije, Robert
Brimioulle, Serge
Dewachter, Laurence
Van Obbergh, Luc
author_facet Boudart, Céline
Su, Fuhong
Herpain, Antoine
Creteur, Jacques
Naeije, Robert
Brimioulle, Serge
Dewachter, Laurence
Van Obbergh, Luc
author_sort Boudart, Céline
collection PubMed
description Coronary blood flow adapts to metabolic demand ("metabolic regulation") and remains relatively constant over a range of pressure changes ("autoregulation"). Coronary metabolic regulation and autoregulation are usually studied separately. We developed an intact animal experimental model to explore both regulatory mechanisms of coronary blood flow. Coronary pressure and flow‐velocities were measured in four anesthetized and closed‐chest pigs using an intracoronary Doppler wire. Metabolic regulation was assessed by coronary flow reserve defined as the ratio between the maximally vasodilated and the basal flow, with hyperemia achieved using intracoronary administration of adenosine (90 µg) or bradykinin (10(–6) M) as endothelium‐independent and ‐dependent vasodilators respectively. For both vasodilators, we found a healthy coronary flow reserve ≥ 3.0 at baseline, which was maintained at 2.9 ± 0.2 after a 6‐hr period. Autoregulation was assessed by the lower breakpoint of coronary pressure‐flow relationships, with gradual decrease in coronary pressure through the inflation of an intracoronary balloon. We found a lower limit of autoregulation between 42 and 55 mmHg, which was stable during a 6‐hr period. We conclude that this intact animal model is adequate for the study of pharmacological interventions on the coronary circulation in health and disease, and as such suitable for preclinical drug studies.
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spelling pubmed-73921302020-08-04 An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation” Boudart, Céline Su, Fuhong Herpain, Antoine Creteur, Jacques Naeije, Robert Brimioulle, Serge Dewachter, Laurence Van Obbergh, Luc Physiol Rep Original Articles Coronary blood flow adapts to metabolic demand ("metabolic regulation") and remains relatively constant over a range of pressure changes ("autoregulation"). Coronary metabolic regulation and autoregulation are usually studied separately. We developed an intact animal experimental model to explore both regulatory mechanisms of coronary blood flow. Coronary pressure and flow‐velocities were measured in four anesthetized and closed‐chest pigs using an intracoronary Doppler wire. Metabolic regulation was assessed by coronary flow reserve defined as the ratio between the maximally vasodilated and the basal flow, with hyperemia achieved using intracoronary administration of adenosine (90 µg) or bradykinin (10(–6) M) as endothelium‐independent and ‐dependent vasodilators respectively. For both vasodilators, we found a healthy coronary flow reserve ≥ 3.0 at baseline, which was maintained at 2.9 ± 0.2 after a 6‐hr period. Autoregulation was assessed by the lower breakpoint of coronary pressure‐flow relationships, with gradual decrease in coronary pressure through the inflation of an intracoronary balloon. We found a lower limit of autoregulation between 42 and 55 mmHg, which was stable during a 6‐hr period. We conclude that this intact animal model is adequate for the study of pharmacological interventions on the coronary circulation in health and disease, and as such suitable for preclinical drug studies. John Wiley and Sons Inc. 2020-07-30 /pmc/articles/PMC7392130/ /pubmed/32729991 http://dx.doi.org/10.14814/phy2.14510 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Boudart, Céline
Su, Fuhong
Herpain, Antoine
Creteur, Jacques
Naeije, Robert
Brimioulle, Serge
Dewachter, Laurence
Van Obbergh, Luc
An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”
title An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”
title_full An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”
title_fullStr An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”
title_full_unstemmed An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”
title_short An intact animal model for the assessment of coronary blood flow regulation “Coronary blood flow regulation”
title_sort intact animal model for the assessment of coronary blood flow regulation “coronary blood flow regulation”
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392130/
https://www.ncbi.nlm.nih.gov/pubmed/32729991
http://dx.doi.org/10.14814/phy2.14510
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