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Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice
Pulmonary hypertension (PH) associated with left heart diseases is the most prevalent cause of PH. The scarcity of studies exploring the pathophysiology and therapies of group II PH resides in the lack of validated small animal models with non-invasive determination of the presence and severity of P...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778040/ https://www.ncbi.nlm.nih.gov/pubmed/29358732 http://dx.doi.org/10.1038/s41598-018-19625-2 |
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author | Dayeh, Nour R. Tardif, Jean-Claude Shi, Yanfen Tanguay, Mégane Ledoux, Jonathan Dupuis, Jocelyn |
author_facet | Dayeh, Nour R. Tardif, Jean-Claude Shi, Yanfen Tanguay, Mégane Ledoux, Jonathan Dupuis, Jocelyn |
author_sort | Dayeh, Nour R. |
collection | PubMed |
description | Pulmonary hypertension (PH) associated with left heart diseases is the most prevalent cause of PH. The scarcity of studies exploring the pathophysiology and therapies of group II PH resides in the lack of validated small animal models with non-invasive determination of the presence and severity of PH. Heart failure (HF) was induced in mice by coronary artery ligation. Mice developed PH as evidenced by an elevated right ventricular (RV) systolic pressure and RV hypertrophy. Detailed non-invasive echocardiographic analysis on the left and right ventricles showed impaired left ventricular (LV) systolic and diastolic function. In addition, RV hypertrophy was confirmed by echo and accompanied by impaired function as well as increased pulmonary resistance. Correlation analysis validated the use of the LV wall-motion score index (WMSI) at a threshold value of ≥2.0 as a powerful and reliable indicator for the presence of PH and RV dysfunction. Echocardiography is an accurate non-invasive technique to diagnose PH in a HF mouse model. Moreover, an echocardiographic parameter of infarct size and LV function, the LV WMSI, reliably correlates with the presence of PH, RV hypertrophy and RV dysfunction and could be used to improve efficiency and design of pre-clinical studies. |
format | Online Article Text |
id | pubmed-5778040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57780402018-01-31 Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice Dayeh, Nour R. Tardif, Jean-Claude Shi, Yanfen Tanguay, Mégane Ledoux, Jonathan Dupuis, Jocelyn Sci Rep Article Pulmonary hypertension (PH) associated with left heart diseases is the most prevalent cause of PH. The scarcity of studies exploring the pathophysiology and therapies of group II PH resides in the lack of validated small animal models with non-invasive determination of the presence and severity of PH. Heart failure (HF) was induced in mice by coronary artery ligation. Mice developed PH as evidenced by an elevated right ventricular (RV) systolic pressure and RV hypertrophy. Detailed non-invasive echocardiographic analysis on the left and right ventricles showed impaired left ventricular (LV) systolic and diastolic function. In addition, RV hypertrophy was confirmed by echo and accompanied by impaired function as well as increased pulmonary resistance. Correlation analysis validated the use of the LV wall-motion score index (WMSI) at a threshold value of ≥2.0 as a powerful and reliable indicator for the presence of PH and RV dysfunction. Echocardiography is an accurate non-invasive technique to diagnose PH in a HF mouse model. Moreover, an echocardiographic parameter of infarct size and LV function, the LV WMSI, reliably correlates with the presence of PH, RV hypertrophy and RV dysfunction and could be used to improve efficiency and design of pre-clinical studies. Nature Publishing Group UK 2018-01-22 /pmc/articles/PMC5778040/ /pubmed/29358732 http://dx.doi.org/10.1038/s41598-018-19625-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dayeh, Nour R. Tardif, Jean-Claude Shi, Yanfen Tanguay, Mégane Ledoux, Jonathan Dupuis, Jocelyn Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
title | Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
title_full | Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
title_fullStr | Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
title_full_unstemmed | Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
title_short | Echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
title_sort | echocardiographic validation of pulmonary hypertension due to heart failure with reduced ejection fraction in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778040/ https://www.ncbi.nlm.nih.gov/pubmed/29358732 http://dx.doi.org/10.1038/s41598-018-19625-2 |
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