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Mitochondrial ROS production, oxidative stress and aging within and between species: Evidences and recent advances on this aging effector

dc.contributor.authorGómez, José
dc.contributor.authorMota Martorell, Natalia
dc.contributor.authorJové, Mariona
dc.contributor.authorPamplona, Reinald
dc.contributor.authorBarja De Quiroga Losada, Gustavo
dc.date.accessioned2023-10-30T18:23:56Z
dc.date.available2023-10-30T18:23:56Z
dc.date.issued2023-02-27
dc.description.abstractMitochondria play a wide diversity of roles in cell physiology and have a key functional implication in cell bioenergetics and biology of free radicals. As the main cellular source of oxygen radicals, mitochondria have been postulated as the mediators of the cellular decline associated with the biological aging. Recent evidences have shown that mitochondrial free radical production is a highly regulated mechanism contributing to the biological determination of longevity which is species-specific. This mitochondrial free radical generation rate induces a diversity of adaptive responses and derived molecular damage to cell components, highlighting mitochondrial DNA damage, with biological consequences that influence the rate of aging of a given animal species. In this review, we explore the idea that mitochondria play a fundamental role in the determination of animal longevity. Once the basic mechanisms are discerned, molecular approaches to counter aging may be designed and developed to prevent or reverse functional decline, and to modify longevity.
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (MICIN)
dc.description.sponsorshipComunidad de Madrid
dc.description.sponsorshipGeneralitat de Catalunya
dc.description.statuspub
dc.identifier.doi10.1016/j.exger.2023.112134
dc.identifier.issn0531-5565
dc.identifier.officialurlhttps://www.sciencedirect.com/science/article/pii/S0531556523000554
dc.identifier.urihttps://hdl.handle.net/20.500.14352/88498
dc.journal.titleExperimental Gerontology
dc.language.isoeng
dc.page.final9
dc.page.initial1
dc.publisherElsevier
dc.relation.projectID(2021SGR00990)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu577.24
dc.subject.cdu576.3
dc.subject.keywordAnimal longevity
dc.subject.keywordComplex I
dc.subject.keywordDNA damage
dc.subject.keywordDNA fragments
dc.subject.keywordElectron transport chain
dc.subject.keywordNDUFV2 subunit
dc.subject.keywordFeS N1a iron-sulfur cluster
dc.subject.keywordAging rate
dc.subject.ucmBiología celular (Biología)
dc.subject.ucmBiología molecular (Biología)
dc.subject.ucmMicrobiología (Biología)
dc.subject.unesco2407.04 Citología
dc.subject.unesco2414 Microbiología
dc.subject.unesco2415 Biología Molecular
dc.titleMitochondrial ROS production, oxidative stress and aging within and between species: Evidences and recent advances on this aging effector
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number174
dspace.entity.typePublication
relation.isAuthorOfPublication832e5933-f640-4442-a205-5872edef1506
relation.isAuthorOfPublication.latestForDiscovery832e5933-f640-4442-a205-5872edef1506

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