Cargando…

An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques

BACKGROUND: Novel cardiovascular magnetic resonance (CMR) techniques and imaging biomarkers are often validated in small animal models or empirically in patients. Direct translation of small animal CMR protocols to humans is rarely possible, while validation in humans is often difficult, slow and oc...

Descripción completa

Detalles Bibliográficos
Autores principales: Schuster, Andreas, Grünwald, Inga, Chiribiri, Amedeo, Southworth, Richard, Ishida, Masaki, Hay, Gunnar, Neumann, Nicole, Morton, Geraint, Perera, Divaka, Schaeffter, Tobias, Nagel, Eike
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950014/
https://www.ncbi.nlm.nih.gov/pubmed/20849589
http://dx.doi.org/10.1186/1532-429X-12-53
_version_ 1782187613127442432
author Schuster, Andreas
Grünwald, Inga
Chiribiri, Amedeo
Southworth, Richard
Ishida, Masaki
Hay, Gunnar
Neumann, Nicole
Morton, Geraint
Perera, Divaka
Schaeffter, Tobias
Nagel, Eike
author_facet Schuster, Andreas
Grünwald, Inga
Chiribiri, Amedeo
Southworth, Richard
Ishida, Masaki
Hay, Gunnar
Neumann, Nicole
Morton, Geraint
Perera, Divaka
Schaeffter, Tobias
Nagel, Eike
author_sort Schuster, Andreas
collection PubMed
description BACKGROUND: Novel cardiovascular magnetic resonance (CMR) techniques and imaging biomarkers are often validated in small animal models or empirically in patients. Direct translation of small animal CMR protocols to humans is rarely possible, while validation in humans is often difficult, slow and occasionally not possible due to ethical considerations. The aim of this study is to overcome these limitations by introducing an MR-compatible, free beating, blood-perfused, isolated pig heart model for the development of novel CMR methodology. METHODS: 6 hearts were perfused outside of the MR environment to establish preparation stability. Coronary perfusion pressure (CPP), coronary blood flow (CBF), left ventricular pressure (LVP), arterial blood gas and electrolyte composition were monitored over 4 hours. Further hearts were perfused within 3T (n = 3) and 1.5T (n = 3) clinical MR scanners, and characterised using functional (CINE), perfusion and late gadolinium enhancement (LGE) imaging. Perfusion imaging was performed globally and selectively for the right (RCA) and left coronary artery (LCA). In one heart the RCA perfusion territory was determined and compared to infarct size after coronary occlusion. RESULTS: All physiological parameters measured remained stable and within normal ranges. The model proved amenable to CMR at both field strengths using typical clinical acquisitions. There was good agreement between the RCA perfusion territory measured by selective first pass perfusion and LGE after coronary occlusion (37% versus 36% of the LV respectively). CONCLUSIONS: This flexible model allows imaging of cardiac function in a controllable, beating, human-sized heart using clinical MR systems. It should aid further development, validation and clinical translation of novel CMR methodologies, and imaging sequences.
format Text
id pubmed-2950014
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-29500142010-10-06 An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques Schuster, Andreas Grünwald, Inga Chiribiri, Amedeo Southworth, Richard Ishida, Masaki Hay, Gunnar Neumann, Nicole Morton, Geraint Perera, Divaka Schaeffter, Tobias Nagel, Eike J Cardiovasc Magn Reson Technical Notes BACKGROUND: Novel cardiovascular magnetic resonance (CMR) techniques and imaging biomarkers are often validated in small animal models or empirically in patients. Direct translation of small animal CMR protocols to humans is rarely possible, while validation in humans is often difficult, slow and occasionally not possible due to ethical considerations. The aim of this study is to overcome these limitations by introducing an MR-compatible, free beating, blood-perfused, isolated pig heart model for the development of novel CMR methodology. METHODS: 6 hearts were perfused outside of the MR environment to establish preparation stability. Coronary perfusion pressure (CPP), coronary blood flow (CBF), left ventricular pressure (LVP), arterial blood gas and electrolyte composition were monitored over 4 hours. Further hearts were perfused within 3T (n = 3) and 1.5T (n = 3) clinical MR scanners, and characterised using functional (CINE), perfusion and late gadolinium enhancement (LGE) imaging. Perfusion imaging was performed globally and selectively for the right (RCA) and left coronary artery (LCA). In one heart the RCA perfusion territory was determined and compared to infarct size after coronary occlusion. RESULTS: All physiological parameters measured remained stable and within normal ranges. The model proved amenable to CMR at both field strengths using typical clinical acquisitions. There was good agreement between the RCA perfusion territory measured by selective first pass perfusion and LGE after coronary occlusion (37% versus 36% of the LV respectively). CONCLUSIONS: This flexible model allows imaging of cardiac function in a controllable, beating, human-sized heart using clinical MR systems. It should aid further development, validation and clinical translation of novel CMR methodologies, and imaging sequences. BioMed Central 2010-09-17 /pmc/articles/PMC2950014/ /pubmed/20849589 http://dx.doi.org/10.1186/1532-429X-12-53 Text en Copyright ©2010 Schuster 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 Technical Notes
Schuster, Andreas
Grünwald, Inga
Chiribiri, Amedeo
Southworth, Richard
Ishida, Masaki
Hay, Gunnar
Neumann, Nicole
Morton, Geraint
Perera, Divaka
Schaeffter, Tobias
Nagel, Eike
An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
title An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
title_full An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
title_fullStr An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
title_full_unstemmed An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
title_short An isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
title_sort isolated perfused pig heart model for the development, validation and translation of novel cardiovascular magnetic resonance techniques
topic Technical Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950014/
https://www.ncbi.nlm.nih.gov/pubmed/20849589
http://dx.doi.org/10.1186/1532-429X-12-53
work_keys_str_mv AT schusterandreas anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT grunwaldinga anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT chiribiriamedeo anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT southworthrichard anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT ishidamasaki anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT haygunnar anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT neumannnicole anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT mortongeraint anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT pereradivaka anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT schaefftertobias anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT nageleike anisolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT schusterandreas isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT grunwaldinga isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT chiribiriamedeo isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT southworthrichard isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT ishidamasaki isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT haygunnar isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT neumannnicole isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT mortongeraint isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT pereradivaka isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT schaefftertobias isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques
AT nageleike isolatedperfusedpigheartmodelforthedevelopmentvalidationandtranslationofnovelcardiovascularmagneticresonancetechniques