Sixty years old is the breakpoint of human frontal cortex aging

dc.contributor.authorCabré, Rosanna
dc.contributor.authorNaudi, Alba
dc.contributor.authorDomínguez González, Mayelín
dc.contributor.authorAyala, Victòria
dc.contributor.authorJove, Mariona
dc.contributor.authorMota-Martorell, Natalia
dc.contributor.authorPiñol Ripoll, Gerard
dc.contributor.authorGil-Villar, Maria Pilar
dc.contributor.authorRué, Montserrat
dc.contributor.authorPortero-Otin, Manuel
dc.contributor.authorFerrer, Isidro (Ferrer Abizanda)
dc.contributor.authorPamplona, Reinald
dc.date.accessioned2019-09-19T14:46:32Z
dc.date.available2019-09-19T14:46:32Z
dc.date.issued2017-02-01
dc.date.updated2019-09-19T14:46:32Z
dc.description.abstractHuman brain aging is the physiological process which underlies as cause of cognitive decline in the elderly and the main risk factor for neurodegenerative diseases such as Alzheimer's disease. Human neurons are functional throughout a healthy adult lifespan, yet the mechanisms that maintain function and protect against neurodegenerative processes during aging are unknown. Here we show that protein oxidative and glycoxidative damage significantly increases during human brain aging, with a breakpoint at 60 years old. This trajectory is coincident with a decrease in the content of the mitochondrial respiratory chain complex I to IV. We suggest that the deterioration in oxidative stress homeostasis during aging induces an adaptive response of stress resistance mechanisms based on the sustained expression of REST, and increased or decreased expression of Akt and mTOR, respectively, over the adult lifespan in order to preserve cell neural survival and function.
dc.format.extent9 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec690147
dc.identifier.issn0891-5849
dc.identifier.pmid27979658
dc.identifier.urihttps://hdl.handle.net/2445/140516
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.freeradbiomed.2016.12.010
dc.relation.ispartofFree Radical Biology and Medicine, 2017, vol. 103, p. 14-22
dc.relation.urihttps://doi.org/10.1016/j.freeradbiomed.2016.12.010
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject.classificationEnvelliment
dc.subject.classificationLòbul frontal
dc.subject.classificationMetabolisme
dc.subject.otherAging
dc.subject.otherFrontal lobe
dc.subject.otherMetabolism
dc.titleSixty years old is the breakpoint of human frontal cortex aging
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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