Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/1365
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dc.contributor.authorLinnane, Anthony-
dc.contributor.authorZhang, Chunfang-
dc.contributor.authorYarovaya, Natalia-
dc.contributor.authorKopsidas, George-
dc.contributor.authorKovalenko, Sergey-
dc.contributor.authorPapakostopoulos, Penny-
dc.contributor.authorEastwood, Hayden-
dc.contributor.authorRichardson, Martin-
dc.contributor.otherGraves, Stephen-
dc.date.accessioned2018-06-01T03:08:46Z-
dc.date.available2018-06-01T03:08:46Z-
dc.date.issued2002-04-
dc.identifier.citationAnn N Y Acad Sci. 2002 Apr; 959: 396-411en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttp://hdl.handle.net/11434/1365-
dc.description.abstractIn this paper, we review two parts of our recent work on human skeletal muscle. The first part mainly describes changes occurring during aging, whereas the second part discusses the functions of coenzyme Q10 (CoQ10), particularly in relation to the aging process. During the lifetime of an individual, mtDNA undergoes a variety of mutation events and rearrangements. These mutations and their consequent bioenergenic decline, together with nuclear DNA damage, contribute to the reduced function of cells and organs, especially in postmitotic tissues. In skeletal muscle, this functional decline can be observed by means of changes with age in fiber type profile and the reduction in the number and size of the muscle fibers. In addition to the functions of coenzyme Q10 as an electron carrier in the respiratory chain and as an antioxidant, CoQ10 has been shown to regulate global gene expression in skeletal muscle. We hypothesize that this regulation is achieved via superoxide formation with H2O2 as a second messenger to the nucleus.en_US
dc.publisherNew York Academy of Sciencesen_US
dc.subjectAgingen_US
dc.subjectPhysiologyen_US
dc.subjectCoenzymesen_US
dc.subjectCytoprotectionen_US
dc.subjectDNA, Mitochondrialen_US
dc.subjectMetabolismen_US
dc.subjectElectron Transport Complex IVen_US
dc.subjectGene Expression Regulationen_US
dc.subjectMuscle, Skeletalen_US
dc.subjectCytologyen_US
dc.subjectEnzymologyen_US
dc.subjectOligonucleotide Array Sequence Analysisen_US
dc.subjectSuccinate Dehydrogenaseen_US
dc.subjectUbiquinoneen_US
dc.subjectAnalogs & Derivativesen_US
dc.subjectCentre for Molecular Biology and Medicine, Epworth Medical Centre, Richmond, Victoria, Australia.en_US
dc.titleHuman aging and global function of coenzyme Q10.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1111/j.1749-6632.2002.tb02110.xen_US
dc.identifier.journaltitleAnnals of the New York Academy of Sciencesen_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/11976213en_US
dc.description.affiliatesRoyal Melbourne Hospital, Orthopaedic Department, Gratten Street, Parkville, Victoria 3052, Australiaen_US
dc.type.studyortrialReviewen_US
dc.type.contenttypeTexten_US
Appears in Collections:Pre-Clinical

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