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Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF
The angiotensin receptor/neprilysin inhibitor Sacubitril/Valsartan (Sac/Val) has been shown to be beneficial in patients suffering from heart failure with reduced ejection fraction (HFrEF). However, the impact of Sac/Val in patients presenting with heart failure with preserved ejection fraction (HFp...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036273/ https://www.ncbi.nlm.nih.gov/pubmed/33808232 http://dx.doi.org/10.3390/ijms22073570 |
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author | Schauer, Antje Adams, Volker Augstein, Antje Jannasch, Anett Draskowski, Runa Kirchhoff, Virginia Goto, Keita Mittag, Jeniffer Galli, Roberta Männel, Anita Barthel, Peggy Linke, Axel Winzer, Ephraim B. |
author_facet | Schauer, Antje Adams, Volker Augstein, Antje Jannasch, Anett Draskowski, Runa Kirchhoff, Virginia Goto, Keita Mittag, Jeniffer Galli, Roberta Männel, Anita Barthel, Peggy Linke, Axel Winzer, Ephraim B. |
author_sort | Schauer, Antje |
collection | PubMed |
description | The angiotensin receptor/neprilysin inhibitor Sacubitril/Valsartan (Sac/Val) has been shown to be beneficial in patients suffering from heart failure with reduced ejection fraction (HFrEF). However, the impact of Sac/Val in patients presenting with heart failure with preserved ejection fraction (HFpEF) is not yet clearly resolved. The present study aimed to reveal the influence of the drug on the functionality of the myocardium, the skeletal muscle, and the vasculature in a rat model of HFpEF. Female obese ZSF-1 rats received Sac/Val as a daily oral gavage for 12 weeks. Left ventricle (LV) function was assessed every four weeks using echocardiography. Prior to organ removal, invasive hemodynamic measurements were performed in both ventricles. Vascular function of the carotid artery and skeletal muscle function were monitored. Sac/Val treatment reduced E/é ratios, left ventricular end diastolic pressure (LVEDP) and myocardial stiffness as well as myocardial fibrosis and heart weight compared to the obese control group. Sac/Val slightly improved endothelial function in the carotid artery but had no impact on skeletal muscle function. Our results demonstrate striking effects of Sac/Val on the myocardial structure and function in a rat model of HFpEF. While vasodilation was slightly improved, functionality of the skeletal muscle remained unaffected. |
format | Online Article Text |
id | pubmed-8036273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80362732021-04-12 Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF Schauer, Antje Adams, Volker Augstein, Antje Jannasch, Anett Draskowski, Runa Kirchhoff, Virginia Goto, Keita Mittag, Jeniffer Galli, Roberta Männel, Anita Barthel, Peggy Linke, Axel Winzer, Ephraim B. Int J Mol Sci Article The angiotensin receptor/neprilysin inhibitor Sacubitril/Valsartan (Sac/Val) has been shown to be beneficial in patients suffering from heart failure with reduced ejection fraction (HFrEF). However, the impact of Sac/Val in patients presenting with heart failure with preserved ejection fraction (HFpEF) is not yet clearly resolved. The present study aimed to reveal the influence of the drug on the functionality of the myocardium, the skeletal muscle, and the vasculature in a rat model of HFpEF. Female obese ZSF-1 rats received Sac/Val as a daily oral gavage for 12 weeks. Left ventricle (LV) function was assessed every four weeks using echocardiography. Prior to organ removal, invasive hemodynamic measurements were performed in both ventricles. Vascular function of the carotid artery and skeletal muscle function were monitored. Sac/Val treatment reduced E/é ratios, left ventricular end diastolic pressure (LVEDP) and myocardial stiffness as well as myocardial fibrosis and heart weight compared to the obese control group. Sac/Val slightly improved endothelial function in the carotid artery but had no impact on skeletal muscle function. Our results demonstrate striking effects of Sac/Val on the myocardial structure and function in a rat model of HFpEF. While vasodilation was slightly improved, functionality of the skeletal muscle remained unaffected. MDPI 2021-03-30 /pmc/articles/PMC8036273/ /pubmed/33808232 http://dx.doi.org/10.3390/ijms22073570 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Schauer, Antje Adams, Volker Augstein, Antje Jannasch, Anett Draskowski, Runa Kirchhoff, Virginia Goto, Keita Mittag, Jeniffer Galli, Roberta Männel, Anita Barthel, Peggy Linke, Axel Winzer, Ephraim B. Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF |
title | Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF |
title_full | Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF |
title_fullStr | Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF |
title_full_unstemmed | Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF |
title_short | Sacubitril/Valsartan Improves Diastolic Function But Not Skeletal Muscle Function in a Rat Model of HFpEF |
title_sort | sacubitril/valsartan improves diastolic function but not skeletal muscle function in a rat model of hfpef |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036273/ https://www.ncbi.nlm.nih.gov/pubmed/33808232 http://dx.doi.org/10.3390/ijms22073570 |
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