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dc.contributor.authorLappalainen, Zekine
dc.date.accessioned2019-10-16T12:01:34Z
dc.date.available2019-10-16T12:01:34Z
dc.date.issued2011en_US
dc.identifier.issn1543-8627
dc.identifier.urihttps://doi.org/10.1080/15438627.2011.536068
dc.identifier.urihttps://hdl.handle.net/20.500.12462/7305
dc.description.abstractThe sirtuin family of proteins consists of seven members in mammals (SirT1-T7). Sirtuins share NAD dependency for their enzymatic activity, but some show NAD-dependent deacetylase activity, others exhibit ADP ribosyltransferase activity or both. Sirtuins have gained considerable attention due to their impact as physiological targets for treating diseases associated with aging. Sirtuins interact with metabolic pathways and may serve as entry points for drugs. This review discusses the biology of sirtuins and their potential as mediators of caloric restriction and pharmacological targets. Reduced insulin sensitivity, mitochondrial dysfunction, and others are consequences of aging or secondary to physical inactivity. Moreover, understanding human energy metabolism through sirtuins may provide a novel approach to exercise physiology. Quercetin, a natural polyphenolic flavonoid that has been widely investigated for its other health benefits, may act as an inducer of SirT1. The benefits of quercetin for exercise performance may have implications for athletes and extended to disease prevention.en_US
dc.language.isoengen_US
dc.publisherRoutledge Journalsen_US
dc.relation.isversionof10.1080/15438627.2011.536068en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectSirtuinsen_US
dc.subjectMetabolismen_US
dc.subjectExerciseen_US
dc.subjectPerformanceen_US
dc.subjectLifespanen_US
dc.titleSirtuins: a family of proteins with ımplications for human performance and exercise physiologyen_US
dc.typeotheren_US
dc.relation.journalResearch in Sports Medicineen_US
dc.contributor.departmentBeden Eğitimi ve Spor Yüksekokuluen_US
dc.identifier.volume19en_US
dc.identifier.issue1en_US
dc.identifier.startpage53en_US
dc.identifier.endpage65en_US
dc.relation.publicationcategoryDiğeren_US


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