Diaphragm myosin heavy chain composition shifts in aging chronically-undernourished Fischer 344 male rats
The effects of chronic undernutrition (UN) on respiratory muscle were investigated during UN producing a 50% decrease in body weight over a prolonged period (45 weeks) in Fischer 344 male rats. This model focused on progressive, aging-related changes in myosin heavy chain (MHC) profile over time, in...
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Veröffentlicht in: | Aging (Milan, Italy) Italy), 1998-04, Vol.10 (2), p.112-119 |
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description | The effects of chronic undernutrition (UN) on respiratory muscle were investigated during UN producing a 50% decrease in body weight over a prolonged period (45 weeks) in Fischer 344 male rats. This model focused on progressive, aging-related changes in myosin heavy chain (MHC) profile over time, in which the confounding effects of early development and late senescence were avoided. With aging toward late adulthood (68 weeks), MHC composition of control diaphragms was shifted, with decreased type I (slow) and IIA MHC, and increased type IIB and IIX (fast) MHC. UN produced a divergence of this profile, with an increase in type I and IIA MHC, and decreased type IIX MHC. UN diaphragms in vitro were more resistant to loss of active force with fatigue, during repetitive contractions. However, passive tension rose disproportionately during fatigue, suggesting increased fatigability. We conclude that the observed changes in diaphragm mechanical function are consistent with the UN-induced shifts in MHC composition; however, the elevated passive tension with fatigue suggests additional UN-induced changes in mechanical properties that are possibly detrimental to respiratory muscle function. The UN-dependent divergence in phenotype and mechanical properties may be amplified by aging-related shifts in muscle MHC composition over time, in the control group. |
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This model focused on progressive, aging-related changes in myosin heavy chain (MHC) profile over time, in which the confounding effects of early development and late senescence were avoided. With aging toward late adulthood (68 weeks), MHC composition of control diaphragms was shifted, with decreased type I (slow) and IIA MHC, and increased type IIB and IIX (fast) MHC. UN produced a divergence of this profile, with an increase in type I and IIA MHC, and decreased type IIX MHC. UN diaphragms in vitro were more resistant to loss of active force with fatigue, during repetitive contractions. However, passive tension rose disproportionately during fatigue, suggesting increased fatigability. We conclude that the observed changes in diaphragm mechanical function are consistent with the UN-induced shifts in MHC composition; however, the elevated passive tension with fatigue suggests additional UN-induced changes in mechanical properties that are possibly detrimental to respiratory muscle function. The UN-dependent divergence in phenotype and mechanical properties may be amplified by aging-related shifts in muscle MHC composition over time, in the control group.</description><identifier>ISSN: 0394-9532</identifier><identifier>ISSN: 1594-0667</identifier><identifier>EISSN: 1720-8319</identifier><identifier>DOI: 10.1007/BF03339645</identifier><identifier>PMID: 9666191</identifier><language>eng</language><publisher>Italy: Springer Nature B.V</publisher><subject>Aging ; Aging - metabolism ; Aging - physiology ; Animals ; Diaphragm - metabolism ; Diaphragm - pathology ; Diaphragm - physiopathology ; Food Deprivation ; Male ; Mechanical properties ; Muscle Contraction ; Muscle Fatigue ; Myosin Heavy Chains - chemistry ; Myosin Heavy Chains - isolation & purification ; Myosin Heavy Chains - metabolism ; Nutrition Disorders - metabolism ; Nutrition Disorders - pathology ; Nutrition Disorders - physiopathology ; Rats ; Rats, Inbred F344 ; Weight Loss</subject><ispartof>Aging (Milan, Italy), 1998-04, Vol.10 (2), p.112-119</ispartof><rights>Aging Clinical and Experimental Research is a copyright of Springer, (1998). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c310t-2212e76a722e2a4811c31f2558edcb8b9ca2a728aa17ee23c78d6522c1cedd713</citedby><cites>FETCH-LOGICAL-c310t-2212e76a722e2a4811c31f2558edcb8b9ca2a728aa17ee23c78d6522c1cedd713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9666191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ameredes, B T</creatorcontrib><creatorcontrib>Rogers, R M</creatorcontrib><creatorcontrib>Donahoe, M P</creatorcontrib><creatorcontrib>Rosas, J F</creatorcontrib><creatorcontrib>Daood, M J</creatorcontrib><creatorcontrib>Watchko, J F</creatorcontrib><title>Diaphragm myosin heavy chain composition shifts in aging chronically-undernourished Fischer 344 male rats</title><title>Aging (Milan, Italy)</title><addtitle>Aging (Milano)</addtitle><description>The effects of chronic undernutrition (UN) on respiratory muscle were investigated during UN producing a 50% decrease in body weight over a prolonged period (45 weeks) in Fischer 344 male rats. This model focused on progressive, aging-related changes in myosin heavy chain (MHC) profile over time, in which the confounding effects of early development and late senescence were avoided. With aging toward late adulthood (68 weeks), MHC composition of control diaphragms was shifted, with decreased type I (slow) and IIA MHC, and increased type IIB and IIX (fast) MHC. UN produced a divergence of this profile, with an increase in type I and IIA MHC, and decreased type IIX MHC. UN diaphragms in vitro were more resistant to loss of active force with fatigue, during repetitive contractions. However, passive tension rose disproportionately during fatigue, suggesting increased fatigability. We conclude that the observed changes in diaphragm mechanical function are consistent with the UN-induced shifts in MHC composition; however, the elevated passive tension with fatigue suggests additional UN-induced changes in mechanical properties that are possibly detrimental to respiratory muscle function. The UN-dependent divergence in phenotype and mechanical properties may be amplified by aging-related shifts in muscle MHC composition over time, in the control group.</description><subject>Aging</subject><subject>Aging - metabolism</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Diaphragm - metabolism</subject><subject>Diaphragm - pathology</subject><subject>Diaphragm - physiopathology</subject><subject>Food Deprivation</subject><subject>Male</subject><subject>Mechanical properties</subject><subject>Muscle Contraction</subject><subject>Muscle Fatigue</subject><subject>Myosin Heavy Chains - chemistry</subject><subject>Myosin Heavy Chains - isolation & purification</subject><subject>Myosin Heavy Chains - metabolism</subject><subject>Nutrition Disorders - metabolism</subject><subject>Nutrition Disorders - pathology</subject><subject>Nutrition Disorders - physiopathology</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Weight Loss</subject><issn>0394-9532</issn><issn>1594-0667</issn><issn>1720-8319</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkc1LAzEQxYMotdRevAsBwYOwmkx2k81Rq1Wh4EXPS5qddlP2oya7wv73RiwKnmZ48-PxZoaQc85uOGPq9n7JhBBaptkRmXIFLMkF18dkyoROE50JOCXzEHaMMZ4qkSo5IRMtpeSaT4l7cGZfebNtaDN2wbW0QvM5UluZ2Nuu2Uexd11LQ-U2faBRNVvXbiPhu9ZZU9djMrQl-rYbvAsVlnTpgq3QU5GmtDE1Um_6cEZONqYOOD_UGXlfPr4tnpPV69PL4m6VWMFZnwBwQCWNAkAwac551DeQZTmWdp2vtTUQh7kxXCGCsCovZQZgucWyVFzMyNWP7953HwOGvmhiHKxr02I3hCKPhxASZAQv_4G7uEEbsxUg0lyD1Boidf1DWd-F4HFT7L1rjB8LzorvBxR_D4jwxcFyWDdY_qKHc4svwkd_0g</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>Ameredes, B T</creator><creator>Rogers, R M</creator><creator>Donahoe, M P</creator><creator>Rosas, J F</creator><creator>Daood, M J</creator><creator>Watchko, J F</creator><general>Springer Nature B.V</general><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>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>19980401</creationdate><title>Diaphragm myosin heavy chain composition shifts in aging chronically-undernourished Fischer 344 male rats</title><author>Ameredes, B T ; Rogers, R M ; Donahoe, M P ; Rosas, J F ; Daood, M J ; Watchko, J F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-2212e76a722e2a4811c31f2558edcb8b9ca2a728aa17ee23c78d6522c1cedd713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Aging</topic><topic>Aging - metabolism</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Diaphragm - metabolism</topic><topic>Diaphragm - pathology</topic><topic>Diaphragm - physiopathology</topic><topic>Food Deprivation</topic><topic>Male</topic><topic>Mechanical properties</topic><topic>Muscle Contraction</topic><topic>Muscle Fatigue</topic><topic>Myosin Heavy Chains - chemistry</topic><topic>Myosin Heavy Chains - isolation & purification</topic><topic>Myosin Heavy Chains - metabolism</topic><topic>Nutrition Disorders - metabolism</topic><topic>Nutrition Disorders - pathology</topic><topic>Nutrition Disorders - physiopathology</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Weight Loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ameredes, B T</creatorcontrib><creatorcontrib>Rogers, R M</creatorcontrib><creatorcontrib>Donahoe, M P</creatorcontrib><creatorcontrib>Rosas, J F</creatorcontrib><creatorcontrib>Daood, M J</creatorcontrib><creatorcontrib>Watchko, J F</creatorcontrib><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>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><jtitle>Aging (Milan, Italy)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ameredes, B T</au><au>Rogers, R M</au><au>Donahoe, M P</au><au>Rosas, J F</au><au>Daood, M J</au><au>Watchko, J F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diaphragm myosin heavy chain composition shifts in aging chronically-undernourished Fischer 344 male rats</atitle><jtitle>Aging (Milan, Italy)</jtitle><addtitle>Aging (Milano)</addtitle><date>1998-04-01</date><risdate>1998</risdate><volume>10</volume><issue>2</issue><spage>112</spage><epage>119</epage><pages>112-119</pages><issn>0394-9532</issn><issn>1594-0667</issn><eissn>1720-8319</eissn><abstract>The effects of chronic undernutrition (UN) on respiratory muscle were investigated during UN producing a 50% decrease in body weight over a prolonged period (45 weeks) in Fischer 344 male rats. This model focused on progressive, aging-related changes in myosin heavy chain (MHC) profile over time, in which the confounding effects of early development and late senescence were avoided. With aging toward late adulthood (68 weeks), MHC composition of control diaphragms was shifted, with decreased type I (slow) and IIA MHC, and increased type IIB and IIX (fast) MHC. UN produced a divergence of this profile, with an increase in type I and IIA MHC, and decreased type IIX MHC. UN diaphragms in vitro were more resistant to loss of active force with fatigue, during repetitive contractions. However, passive tension rose disproportionately during fatigue, suggesting increased fatigability. We conclude that the observed changes in diaphragm mechanical function are consistent with the UN-induced shifts in MHC composition; however, the elevated passive tension with fatigue suggests additional UN-induced changes in mechanical properties that are possibly detrimental to respiratory muscle function. The UN-dependent divergence in phenotype and mechanical properties may be amplified by aging-related shifts in muscle MHC composition over time, in the control group.</abstract><cop>Italy</cop><pub>Springer Nature B.V</pub><pmid>9666191</pmid><doi>10.1007/BF03339645</doi><tpages>8</tpages></addata></record> |
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subjects | Aging Aging - metabolism Aging - physiology Animals Diaphragm - metabolism Diaphragm - pathology Diaphragm - physiopathology Food Deprivation Male Mechanical properties Muscle Contraction Muscle Fatigue Myosin Heavy Chains - chemistry Myosin Heavy Chains - isolation & purification Myosin Heavy Chains - metabolism Nutrition Disorders - metabolism Nutrition Disorders - pathology Nutrition Disorders - physiopathology Rats Rats, Inbred F344 Weight Loss |
title | Diaphragm myosin heavy chain composition shifts in aging chronically-undernourished Fischer 344 male rats |
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