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Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology
Background. Heart development is a complex process, and abnormal development may result in congenital heart disease (CHD). Currently, studies on animal models mainly focus on cardiac morphology and the availability of hemodynamic data, especially of the right heart half, is limited. Here we aimed to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951091/ https://www.ncbi.nlm.nih.gov/pubmed/24707208 http://dx.doi.org/10.1155/2014/531324 |
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author | Hahurij, Nathan D. Calkoen, Emmeline E. Jongbloed, Monique R. M. Roest, Arno A. W. Gittenberger-de Groot, Adriana C. Poelmann, Robert E. De Ruiter, Marco C. van Munsteren, Conny J. Steendijk, Paul Blom, Nico A. |
author_facet | Hahurij, Nathan D. Calkoen, Emmeline E. Jongbloed, Monique R. M. Roest, Arno A. W. Gittenberger-de Groot, Adriana C. Poelmann, Robert E. De Ruiter, Marco C. van Munsteren, Conny J. Steendijk, Paul Blom, Nico A. |
author_sort | Hahurij, Nathan D. |
collection | PubMed |
description | Background. Heart development is a complex process, and abnormal development may result in congenital heart disease (CHD). Currently, studies on animal models mainly focus on cardiac morphology and the availability of hemodynamic data, especially of the right heart half, is limited. Here we aimed to assess the morphological and hemodynamic parameters of normal developing mouse embryos/fetuses by using a high-frequency ultrasound system. Methods. A timed breeding program was initiated with a WT mouse line (Swiss/129Sv background). All recordings were performed transabdominally, in isoflurane sedated pregnant mice, in hearts of sequential developmental stages: 12.5, 14.5, and 17.5 days after conception (n = 105). Results. Along development the heart rate increased significantly from 125 ± 9.5 to 219 ± 8.3 beats per minute. Reliable flow measurements could be performed across the developing mitral and tricuspid valves and outflow tract. M-mode measurements could be obtained of all cardiac compartments. An overall increase of cardiac systolic and diastolic function with embryonic/fetal development was observed. Conclusion. High-frequency echocardiography is a promising and useful imaging modality for structural and hemodynamic analysis of embryonic/fetal mouse hearts. |
format | Online Article Text |
id | pubmed-3951091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39510912014-04-06 Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology Hahurij, Nathan D. Calkoen, Emmeline E. Jongbloed, Monique R. M. Roest, Arno A. W. Gittenberger-de Groot, Adriana C. Poelmann, Robert E. De Ruiter, Marco C. van Munsteren, Conny J. Steendijk, Paul Blom, Nico A. ScientificWorldJournal Research Article Background. Heart development is a complex process, and abnormal development may result in congenital heart disease (CHD). Currently, studies on animal models mainly focus on cardiac morphology and the availability of hemodynamic data, especially of the right heart half, is limited. Here we aimed to assess the morphological and hemodynamic parameters of normal developing mouse embryos/fetuses by using a high-frequency ultrasound system. Methods. A timed breeding program was initiated with a WT mouse line (Swiss/129Sv background). All recordings were performed transabdominally, in isoflurane sedated pregnant mice, in hearts of sequential developmental stages: 12.5, 14.5, and 17.5 days after conception (n = 105). Results. Along development the heart rate increased significantly from 125 ± 9.5 to 219 ± 8.3 beats per minute. Reliable flow measurements could be performed across the developing mitral and tricuspid valves and outflow tract. M-mode measurements could be obtained of all cardiac compartments. An overall increase of cardiac systolic and diastolic function with embryonic/fetal development was observed. Conclusion. High-frequency echocardiography is a promising and useful imaging modality for structural and hemodynamic analysis of embryonic/fetal mouse hearts. Hindawi Publishing Corporation 2014-02-23 /pmc/articles/PMC3951091/ /pubmed/24707208 http://dx.doi.org/10.1155/2014/531324 Text en Copyright © 2014 Nathan D. Hahurij et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hahurij, Nathan D. Calkoen, Emmeline E. Jongbloed, Monique R. M. Roest, Arno A. W. Gittenberger-de Groot, Adriana C. Poelmann, Robert E. De Ruiter, Marco C. van Munsteren, Conny J. Steendijk, Paul Blom, Nico A. Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology |
title | Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology |
title_full | Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology |
title_fullStr | Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology |
title_full_unstemmed | Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology |
title_short | Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology |
title_sort | echocardiographic assessment of embryonic and fetal mouse heart development: a focus on haemodynamics and morphology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951091/ https://www.ncbi.nlm.nih.gov/pubmed/24707208 http://dx.doi.org/10.1155/2014/531324 |
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