<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Saw EL</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>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 &lt;i>SAUNA&lt;/i> (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, &lt;i>soleus&lt;/i> muscle) has not been described in this preclinical HFpEF model. We sought to characterize the &lt;i>soleus&lt;/i> skeletal muscle in the HFpEF &lt;i>SAUNA&lt;/i> mice and investigate its translational potential.&lt;h4>Methods&lt;/h4>HFpEF was indu</pubmed_abstract><journal>Frontiers in cardiovascular medicine</journal><pagination>1016452</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9753550</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction.</pubmed_title><pmcid>PMC9753550</pmcid><pubmed_authors>Valero-Munoz M</pubmed_authors><pubmed_authors>Saw EL</pubmed_authors><pubmed_authors>Werner LD</pubmed_authors><pubmed_authors>Zamani P</pubmed_authors><pubmed_authors>Sam F</pubmed_authors><pubmed_authors>Chirinos JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Skeletal muscle phenotypic switching in heart failure with preserved ejection fraction.</name><description>&lt;h4>Background&lt;/h4>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 &lt;i>SAUNA&lt;/i> (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, &lt;i>soleus&lt;/i> muscle) has not been described in this preclinical HFpEF model. We sought to characterize the &lt;i>soleus&lt;/i> skeletal muscle in the HFpEF &lt;i>SAUNA&lt;/i> mice and investigate its translational potential.&lt;h4>Methods&lt;/h4>HFpEF was indu</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-18T16:31:22.59Z</modification><creation>2025-04-07T03:44:28.427Z</creation></dates><accession>S-EPMC9753550</accession><cross_references><pubmed>36531739</pubmed><doi>10.3389/fcvm.2022.1016452</doi></cross_references></HashMap>