Show simple item record

dc.contributor.authorWall, BT
dc.contributor.authorDirks, ML
dc.contributor.authorSnijders, T
dc.contributor.authorStephens, FB
dc.contributor.authorSenden, JMG
dc.contributor.authorVerscheijden, M-L
dc.contributor.authorvan Loon, LJC
dc.date.accessioned2017-04-03T14:55:32Z
dc.date.issued2015-01
dc.description.abstractAging is generally accompanied by a progressive loss of skeletal muscle mass and impairments in metabolic function. Even a few days of muscle disuse (such as that occurring during injury or illness) leads to considerable loss of muscle mass and strength. It has been speculated that short, successive periods of muscle disuse throughout the lifespan may be largely responsible for the age-related loss of muscle mass. However, it remains unknown whether such short periods of disuse also induce impairments in metabolic function within skeletal muscle. Here, we investigated the effects of a five day period of muscle disuse on intramyocellular triacylglycerol (IMTG) content, muscle oxidative capacity, and the expression of key genes that regulate oxidative metabolism in healthy young and elderly men. Muscle biopsies were collected from healthy, young (n=12; 23±1y) and elderly (n=12; 70±1y) men prior to and immediately after a five day period of one-legged knee immobilization by way of a full leg cast. At baseline, elderly men had a greater IMTG content when compared with the young (56.2±5.1 and 34.8±7.3μmol·g(-1), respectively; P<0.05) with no changes in either group following immobilization (53.4±5.0 and 35.7±5.0μmol·g(-1), respectively; P>0.05). In line, five days of disuse did not lower citrate synthase, β-HAD or cytochrome C oxidase activity in skeletal muscle tissue. Pyruvate dehydrogenase activity increased following immobilization in the older subjects only, from 0.39±0.06 to 0.55 0.05μmol·g(-1)·min(-1) (71±33%; P<0.01). The skeletal muscle mRNA expression of PGC1α and citrate synthase both declined following immobilization in both the young and elderly subjects. We conclude that five days of muscle disuse does not increase intramuscular lipid deposition or reduce the maximal activity of key mitochondrial enzymes within the skeletal muscle of young or older men.en_GB
dc.identifier.citationVol. 61, pp. 76 - 83en_GB
dc.identifier.doi10.1016/j.exger.2014.11.019
dc.identifier.otherS0531-5565(14)00345-3
dc.identifier.urihttp://hdl.handle.net/10871/26942
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/25457674en_GB
dc.subjectAgingen_GB
dc.subjectDisuseen_GB
dc.subjectImmobilizationen_GB
dc.subjectLipidsen_GB
dc.subjectOxidative capacityen_GB
dc.subjectSarcopeniaen_GB
dc.subjectSkeletal muscleen_GB
dc.subjectAdulten_GB
dc.subjectAgeden_GB
dc.subjectAgingen_GB
dc.subjectBody Compositionen_GB
dc.subjectCitrate (si)-Synthaseen_GB
dc.subjectHumansen_GB
dc.subjectInsulin Resistanceen_GB
dc.subjectLipid Metabolismen_GB
dc.subjectMaleen_GB
dc.subjectMitochondria, Muscleen_GB
dc.subjectMuscle Strengthen_GB
dc.subjectMuscle, Skeletalen_GB
dc.subjectMuscular Atrophyen_GB
dc.subjectPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaen_GB
dc.subjectPyruvate Dehydrogenase Complexen_GB
dc.subjectRNA, Messengeren_GB
dc.subjectTranscription Factorsen_GB
dc.subjectTriglyceridesen_GB
dc.titleShort-term muscle disuse atrophy is not associated with increased intramuscular lipid deposition or a decline in the maximal activity of key mitochondrial enzymes in young and older malesen_GB
dc.typeArticleen_GB
dc.date.available2017-04-03T14:55:32Z
dc.identifier.issn0531-5565
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the author accepted manuscript. The final version is available from the publisher via the DOI in this record.en_GB
dc.identifier.journalExperimental Gerontologyen_GB
dc.identifier.pmid25457674


Files in this item

This item appears in the following Collection(s)

Show simple item record