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Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction

BACKGROUND: Skeletal muscle (SkM) phenotypic switching is associated with exercise intolerance in heart failure with preserved ejection fraction (HFpEF). Patients with HFpEF have decreased type-1 oxidative fibers and mitochondrial dysfunction, indicative of impaired oxidative capacity. The SAUNA (SA...

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Autores principales: Saw, Eng Leng, Werner, Louis Dominic, Zamani, Payman, Chirinos, Julio A., Valero-Muñoz, María, Sam, Flora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753550/
https://www.ncbi.nlm.nih.gov/pubmed/36531739
http://dx.doi.org/10.3389/fcvm.2022.1016452
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author Saw, Eng Leng
Werner, Louis Dominic
Zamani, Payman
Chirinos, Julio A.
Valero-Muñoz, María
Sam, Flora
author_facet Saw, Eng Leng
Werner, Louis Dominic
Zamani, Payman
Chirinos, Julio A.
Valero-Muñoz, María
Sam, Flora
author_sort Saw, Eng Leng
collection PubMed
description BACKGROUND: Skeletal muscle (SkM) phenotypic switching is associated with exercise intolerance in heart failure with preserved ejection fraction (HFpEF). Patients with HFpEF have decreased type-1 oxidative fibers and mitochondrial dysfunction, indicative of impaired oxidative capacity. The SAUNA (SAlty drinking water/Unilateral Nephrectomy/Aldosterone) mice are commonly used in HFpEF pre-clinical studies and demonstrate cardiac, lung, kidney, and white adipose tissue impairments. However, the SkM (specifically the oxidative-predominant, soleus muscle) has not been described in this preclinical HFpEF model. We sought to characterize the soleus skeletal muscle in the HFpEF SAUNA mice and investigate its translational potential. METHODS: HFpEF was induced in mice by uninephrectomy, d-aldosterone or saline (Sham) infusion by osmotic pump implantation, and 1% NaCl drinking water was given for 4 weeks. Mice were euthanized, and the oxidative-predominant soleus muscle was collected. We examined fiber composition, fiber cross-sectional area, capillary density, and fibrosis. Molecular analyses were also performed. To investigate the clinical relevance of this model, the oxidative-predominant, vastus lateralis muscle from patients with HFpEF was biopsied and examined for molecular changes in mitochondrial oxidative phosphorylation, vasculature, fibrosis, and inflammation. RESULTS: Histological analyses demonstrated a reduction in the abundance of oxidative fibers, type-2A fiber atrophy, decreased capillary density, and increased fibrotic area in the soleus muscle of HFpEF mice compared to Sham. Expression of targets of interest such as a reduction in mitochondrial oxidative-phosphorylation genes, increased VEGF-α and an elevated inflammatory response was also seen. The histological and molecular changes in HFpEF mice are consistent and comparable with changes seen in the oxidative-predominant SkM of patients with HFpEF. CONCLUSION: The HFpEF SAUNA model recapitulates the SkM phenotypic switching seen in HFpEF patients. This model is suitable and relevant to study SkM phenotypic switching in HFpEF.
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spelling pubmed-97535502022-12-16 Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction Saw, Eng Leng Werner, Louis Dominic Zamani, Payman Chirinos, Julio A. Valero-Muñoz, María Sam, Flora Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Skeletal muscle (SkM) phenotypic switching is associated with exercise intolerance in heart failure with preserved ejection fraction (HFpEF). Patients with HFpEF have decreased type-1 oxidative fibers and mitochondrial dysfunction, indicative of impaired oxidative capacity. The SAUNA (SAlty drinking water/Unilateral Nephrectomy/Aldosterone) mice are commonly used in HFpEF pre-clinical studies and demonstrate cardiac, lung, kidney, and white adipose tissue impairments. However, the SkM (specifically the oxidative-predominant, soleus muscle) has not been described in this preclinical HFpEF model. We sought to characterize the soleus skeletal muscle in the HFpEF SAUNA mice and investigate its translational potential. METHODS: HFpEF was induced in mice by uninephrectomy, d-aldosterone or saline (Sham) infusion by osmotic pump implantation, and 1% NaCl drinking water was given for 4 weeks. Mice were euthanized, and the oxidative-predominant soleus muscle was collected. We examined fiber composition, fiber cross-sectional area, capillary density, and fibrosis. Molecular analyses were also performed. To investigate the clinical relevance of this model, the oxidative-predominant, vastus lateralis muscle from patients with HFpEF was biopsied and examined for molecular changes in mitochondrial oxidative phosphorylation, vasculature, fibrosis, and inflammation. RESULTS: Histological analyses demonstrated a reduction in the abundance of oxidative fibers, type-2A fiber atrophy, decreased capillary density, and increased fibrotic area in the soleus muscle of HFpEF mice compared to Sham. Expression of targets of interest such as a reduction in mitochondrial oxidative-phosphorylation genes, increased VEGF-α and an elevated inflammatory response was also seen. The histological and molecular changes in HFpEF mice are consistent and comparable with changes seen in the oxidative-predominant SkM of patients with HFpEF. CONCLUSION: The HFpEF SAUNA model recapitulates the SkM phenotypic switching seen in HFpEF patients. This model is suitable and relevant to study SkM phenotypic switching in HFpEF. Frontiers Media S.A. 2022-12-01 /pmc/articles/PMC9753550/ /pubmed/36531739 http://dx.doi.org/10.3389/fcvm.2022.1016452 Text en Copyright © 2022 Saw, Werner, Zamani, Chirinos, Valero-Muñoz and Sam. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Saw, Eng Leng
Werner, Louis Dominic
Zamani, Payman
Chirinos, Julio A.
Valero-Muñoz, María
Sam, Flora
Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
title Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
title_full Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
title_fullStr Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
title_full_unstemmed Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
title_short Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
title_sort skeletal muscle phenotypic switching in heart failure with preserved ejection fraction
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753550/
https://www.ncbi.nlm.nih.gov/pubmed/36531739
http://dx.doi.org/10.3389/fcvm.2022.1016452
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