High‐fat diet affects skeletal muscle mitochondria comparable to pressure overload‐induced heart failure
In heart failure, high‐fat diet (HFD) may exert beneficial effects on cardiac mitochondria and contractility. Skeletal muscle mitochondrial dysfunction in heart failure is associated with myopathy. However, it is not clear if HFD affects skeletal muscle mitochondria in heart failure as well. To indu...
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description | In heart failure, high‐fat diet (HFD) may exert beneficial effects on cardiac mitochondria and contractility. Skeletal muscle mitochondrial dysfunction in heart failure is associated with myopathy. However, it is not clear if HFD affects skeletal muscle mitochondria in heart failure as well. To induce heart failure, we used pressure overload (PO) in rats fed normal chow or HFD. Interfibrillar mitochondria (IFM) and subsarcolemmal mitochondria (SSM) from gastrocnemius were isolated and functionally characterized. With PO heart failure, maximal respiratory capacity was impaired in IFM but increased in SSM of gastrocnemius. Unexpectedly, HFD affected mitochondria comparably to PO. In combination, PO and HFD showed additive effects on mitochondrial subpopulations which were reflected by isolated complex activities. While PO impaired diastolic as well as systolic cardiac function and increased glucose tolerance, HFD did not affect cardiac function but decreased glucose tolerance. We conclude that HFD and PO heart failure have comparable effects leading to more severe impairment of IFM. Glucose tolerance seems not causally related to skeletal muscle mitochondrial dysfunction. The additive effects of HFD and PO may suggest accelerated skeletal muscle mitochondrial dysfunction when heart failure is accompanied with a diet containing high fat. |
doi_str_mv | 10.1111/jcmm.15325 |
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Skeletal muscle mitochondrial dysfunction in heart failure is associated with myopathy. However, it is not clear if HFD affects skeletal muscle mitochondria in heart failure as well. To induce heart failure, we used pressure overload (PO) in rats fed normal chow or HFD. Interfibrillar mitochondria (IFM) and subsarcolemmal mitochondria (SSM) from gastrocnemius were isolated and functionally characterized. With PO heart failure, maximal respiratory capacity was impaired in IFM but increased in SSM of gastrocnemius. Unexpectedly, HFD affected mitochondria comparably to PO. In combination, PO and HFD showed additive effects on mitochondrial subpopulations which were reflected by isolated complex activities. While PO impaired diastolic as well as systolic cardiac function and increased glucose tolerance, HFD did not affect cardiac function but decreased glucose tolerance. We conclude that HFD and PO heart failure have comparable effects leading to more severe impairment of IFM. Glucose tolerance seems not causally related to skeletal muscle mitochondrial dysfunction. The additive effects of HFD and PO may suggest accelerated skeletal muscle mitochondrial dysfunction when heart failure is accompanied with a diet containing high fat.</description><identifier>ISSN: 1582-1838</identifier><identifier>EISSN: 1582-4934</identifier><identifier>DOI: 10.1111/jcmm.15325</identifier><identifier>PMID: 32363733</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adenosine diphosphate ; Adenosine Diphosphate - metabolism ; Adenosine triphosphate ; Age ; Animal care ; Animals ; Body Weight ; Carbohydrates ; Cell Respiration ; Congestive heart failure ; Cytochrome ; Diet, High-Fat ; Electrocardiography ; Glucose ; Glucose tolerance ; Heart failure ; Heart Failure - diagnostic imaging ; Heart Failure - pathology ; High fat diet ; interfibrillar/subsarcolemmal mitochondria ; Laboratory animals ; Male ; Mitochondria ; Mitochondria, Muscle - pathology ; Muscle contraction ; Muscle, Skeletal - diagnostic imaging ; Muscle, Skeletal - pathology ; Musculoskeletal system ; Myopathy ; Original ; Oxygen Consumption ; Pressure ; pressure overload ; Proteins ; Rats, Sprague-Dawley ; Skeletal muscle ; Subpopulations ; Surgery ; Sutures</subject><ispartof>Journal of cellular and molecular medicine, 2020-06, Vol.24 (12), p.6741-6749</ispartof><rights>2020 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd</rights><rights>2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5145-a798d80811525ad849b932789fdb4826b9525311708d5b359f5fa3c6aee511d3</citedby><cites>FETCH-LOGICAL-c5145-a798d80811525ad849b932789fdb4826b9525311708d5b359f5fa3c6aee511d3</cites><orcidid>0000-0002-1401-4679 ; 0000-0001-9698-4830</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299710/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299710/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,1414,11545,27907,27908,45557,45558,46035,46459,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32363733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heyne, Estelle</creatorcontrib><creatorcontrib>Schrepper, Andrea</creatorcontrib><creatorcontrib>Doenst, Torsten</creatorcontrib><creatorcontrib>Schenkl, Christina</creatorcontrib><creatorcontrib>Kreuzer, Katrin</creatorcontrib><creatorcontrib>Schwarzer, Michael</creatorcontrib><title>High‐fat diet affects skeletal muscle mitochondria comparable to pressure overload‐induced heart failure</title><title>Journal of cellular and molecular medicine</title><addtitle>J Cell Mol Med</addtitle><description>In heart failure, high‐fat diet (HFD) may exert beneficial effects on cardiac mitochondria and contractility. Skeletal muscle mitochondrial dysfunction in heart failure is associated with myopathy. However, it is not clear if HFD affects skeletal muscle mitochondria in heart failure as well. To induce heart failure, we used pressure overload (PO) in rats fed normal chow or HFD. Interfibrillar mitochondria (IFM) and subsarcolemmal mitochondria (SSM) from gastrocnemius were isolated and functionally characterized. With PO heart failure, maximal respiratory capacity was impaired in IFM but increased in SSM of gastrocnemius. Unexpectedly, HFD affected mitochondria comparably to PO. In combination, PO and HFD showed additive effects on mitochondrial subpopulations which were reflected by isolated complex activities. While PO impaired diastolic as well as systolic cardiac function and increased glucose tolerance, HFD did not affect cardiac function but decreased glucose tolerance. We conclude that HFD and PO heart failure have comparable effects leading to more severe impairment of IFM. Glucose tolerance seems not causally related to skeletal muscle mitochondrial dysfunction. The additive effects of HFD and PO may suggest accelerated skeletal muscle mitochondrial dysfunction when heart failure is accompanied with a diet containing high fat.</description><subject>Adenosine diphosphate</subject><subject>Adenosine Diphosphate - metabolism</subject><subject>Adenosine triphosphate</subject><subject>Age</subject><subject>Animal care</subject><subject>Animals</subject><subject>Body Weight</subject><subject>Carbohydrates</subject><subject>Cell Respiration</subject><subject>Congestive heart failure</subject><subject>Cytochrome</subject><subject>Diet, High-Fat</subject><subject>Electrocardiography</subject><subject>Glucose</subject><subject>Glucose tolerance</subject><subject>Heart failure</subject><subject>Heart Failure - diagnostic imaging</subject><subject>Heart Failure - pathology</subject><subject>High fat diet</subject><subject>interfibrillar/subsarcolemmal mitochondria</subject><subject>Laboratory animals</subject><subject>Male</subject><subject>Mitochondria</subject><subject>Mitochondria, Muscle - pathology</subject><subject>Muscle contraction</subject><subject>Muscle, Skeletal - diagnostic imaging</subject><subject>Muscle, Skeletal - pathology</subject><subject>Musculoskeletal system</subject><subject>Myopathy</subject><subject>Original</subject><subject>Oxygen Consumption</subject><subject>Pressure</subject><subject>pressure overload</subject><subject>Proteins</subject><subject>Rats, Sprague-Dawley</subject><subject>Skeletal muscle</subject><subject>Subpopulations</subject><subject>Surgery</subject><subject>Sutures</subject><issn>1582-1838</issn><issn>1582-4934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1uFDEQRlsIRH5gwwGQJTZRpAlddnva3iChERBQIjbZW267nPHgbg-2Oyi7HIEzchIcZoiABd6UVfX0VKWvaV5Aewb1vd6YcTwDzih_1BwCF3TRSdY93v9BMHHQHOW8aVu2BCafNgeMsiXrGTtswrm_Xv-4--50IdZjIdo5NCWT_AUDFh3IOGcTkIy-RLOOk01eExPHrU56qP0SyTZhznNCEm8whaht9fnJzgYtWaNOhTjtQwWeNU-cDhmf7-txc_X-3dXqfHHx-cPH1duLheHQ8YXupbCiFQCccm1FJwfJaC-ks0Mn6HKQtc8A-lZYPjAuHXeamaVG5ACWHTdvdtrtPIxoDU4l6aC2yY863aqovfp7Mvm1uo43qqdS9tBWwclekOLXGXNRo88GQ9ATxjkryqQA3vdSVvTVP-gmzmmq1ynaQVdlrWCVOt1RJsWcE7qHZaBV9xmq-wzVrwwr_PLP9R_Q36FVAHbANx_w9j8q9Wl1ebmT_gTAB6p6</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Heyne, Estelle</creator><creator>Schrepper, Andrea</creator><creator>Doenst, Torsten</creator><creator>Schenkl, Christina</creator><creator>Kreuzer, Katrin</creator><creator>Schwarzer, Michael</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1401-4679</orcidid><orcidid>https://orcid.org/0000-0001-9698-4830</orcidid></search><sort><creationdate>202006</creationdate><title>High‐fat diet affects skeletal muscle mitochondria comparable to pressure overload‐induced heart failure</title><author>Heyne, Estelle ; Schrepper, Andrea ; Doenst, Torsten ; Schenkl, Christina ; Kreuzer, Katrin ; Schwarzer, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5145-a798d80811525ad849b932789fdb4826b9525311708d5b359f5fa3c6aee511d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adenosine diphosphate</topic><topic>Adenosine Diphosphate - metabolism</topic><topic>Adenosine triphosphate</topic><topic>Age</topic><topic>Animal care</topic><topic>Animals</topic><topic>Body Weight</topic><topic>Carbohydrates</topic><topic>Cell Respiration</topic><topic>Congestive heart failure</topic><topic>Cytochrome</topic><topic>Diet, High-Fat</topic><topic>Electrocardiography</topic><topic>Glucose</topic><topic>Glucose tolerance</topic><topic>Heart failure</topic><topic>Heart Failure - diagnostic imaging</topic><topic>Heart Failure - pathology</topic><topic>High fat diet</topic><topic>interfibrillar/subsarcolemmal mitochondria</topic><topic>Laboratory animals</topic><topic>Male</topic><topic>Mitochondria</topic><topic>Mitochondria, Muscle - pathology</topic><topic>Muscle contraction</topic><topic>Muscle, Skeletal - diagnostic imaging</topic><topic>Muscle, Skeletal - pathology</topic><topic>Musculoskeletal system</topic><topic>Myopathy</topic><topic>Original</topic><topic>Oxygen Consumption</topic><topic>Pressure</topic><topic>pressure overload</topic><topic>Proteins</topic><topic>Rats, Sprague-Dawley</topic><topic>Skeletal muscle</topic><topic>Subpopulations</topic><topic>Surgery</topic><topic>Sutures</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heyne, Estelle</creatorcontrib><creatorcontrib>Schrepper, Andrea</creatorcontrib><creatorcontrib>Doenst, Torsten</creatorcontrib><creatorcontrib>Schenkl, Christina</creatorcontrib><creatorcontrib>Kreuzer, Katrin</creatorcontrib><creatorcontrib>Schwarzer, Michael</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cellular and molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heyne, Estelle</au><au>Schrepper, Andrea</au><au>Doenst, Torsten</au><au>Schenkl, Christina</au><au>Kreuzer, Katrin</au><au>Schwarzer, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High‐fat diet affects skeletal muscle mitochondria comparable to pressure overload‐induced heart failure</atitle><jtitle>Journal of cellular and molecular medicine</jtitle><addtitle>J Cell Mol Med</addtitle><date>2020-06</date><risdate>2020</risdate><volume>24</volume><issue>12</issue><spage>6741</spage><epage>6749</epage><pages>6741-6749</pages><issn>1582-1838</issn><eissn>1582-4934</eissn><abstract>In heart failure, high‐fat diet (HFD) may exert beneficial effects on cardiac mitochondria and contractility. Skeletal muscle mitochondrial dysfunction in heart failure is associated with myopathy. However, it is not clear if HFD affects skeletal muscle mitochondria in heart failure as well. To induce heart failure, we used pressure overload (PO) in rats fed normal chow or HFD. Interfibrillar mitochondria (IFM) and subsarcolemmal mitochondria (SSM) from gastrocnemius were isolated and functionally characterized. With PO heart failure, maximal respiratory capacity was impaired in IFM but increased in SSM of gastrocnemius. Unexpectedly, HFD affected mitochondria comparably to PO. In combination, PO and HFD showed additive effects on mitochondrial subpopulations which were reflected by isolated complex activities. While PO impaired diastolic as well as systolic cardiac function and increased glucose tolerance, HFD did not affect cardiac function but decreased glucose tolerance. We conclude that HFD and PO heart failure have comparable effects leading to more severe impairment of IFM. Glucose tolerance seems not causally related to skeletal muscle mitochondrial dysfunction. The additive effects of HFD and PO may suggest accelerated skeletal muscle mitochondrial dysfunction when heart failure is accompanied with a diet containing high fat.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>32363733</pmid><doi>10.1111/jcmm.15325</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1401-4679</orcidid><orcidid>https://orcid.org/0000-0001-9698-4830</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine diphosphate Adenosine Diphosphate - metabolism Adenosine triphosphate Age Animal care Animals Body Weight Carbohydrates Cell Respiration Congestive heart failure Cytochrome Diet, High-Fat Electrocardiography Glucose Glucose tolerance Heart failure Heart Failure - diagnostic imaging Heart Failure - pathology High fat diet interfibrillar/subsarcolemmal mitochondria Laboratory animals Male Mitochondria Mitochondria, Muscle - pathology Muscle contraction Muscle, Skeletal - diagnostic imaging Muscle, Skeletal - pathology Musculoskeletal system Myopathy Original Oxygen Consumption Pressure pressure overload Proteins Rats, Sprague-Dawley Skeletal muscle Subpopulations Surgery Sutures |
title | High‐fat diet affects skeletal muscle mitochondria comparable to pressure overload‐induced heart failure |
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