Characterization of a natural model of adult mice with different rate of aging

dc.contributor.authorFélix, Judith
dc.contributor.authorDíaz del Cerro, Estefanía
dc.contributor.authorGarrido Garrío, Antonio
dc.contributor.authorFuente, Mónica de la
dc.date.accessioned2024-09-21T11:07:14Z
dc.date.available2024-09-21T11:07:14Z
dc.date.issued2024
dc.description.abstractAging is a heterogeneous process, so individuals of the same age may be aging at a different rate. A natural model of premature aging in mice have been proposed based on the poor response to the T-maze. Those that take longer to cross the intersection are known as Prematurely Aging Mice (PAM), while those that show an exceptional response are known as Exceptional non-PAM (E-NPAM), being the rest non-PAM (NPAM). Although many aspects of PAM and E-NPAM have been described, some aspects of their brain aging have not been studied. Similarly, it is known that PAM, NPAM and E-NPAM show a different rate of aging and longevity, but the differences between these three groups in behavior, immune function and oxidative-inflammatory state are unknown. The present study aims to deepen the study of brain aging in PAM and E-NPAM, and to study the differences in behavior, immunity, and oxidative-inflammatory state of peritoneal leukocytes between PAM, NPAM and E-NPAM. Results show deteriorated brains in PAM. Moreover, NPAM show an oxidative state similar to E-NPAM, an anxiety similar to PAM, and an intermediate immunity and lifespan between PAM and E-NPAM. In conclusion, immune function seems to be more associated with the longevity achieved.spa
dc.description.filiationUEMspa
dc.description.impact5.3 Q2 JCR 2023spa
dc.description.impact1.577 Q1 SJR 2023spa
dc.description.impactNo data IDR 2023spa
dc.description.sponsorshipThis research was funded by the Research Group UCM ( 910379 ).spa
dc.identifier.citationFélix, J., Díaz Del Cerro, E., Garrido, A., & Fuente, M. (2024). Characterization of a natural model of adult mice with different rate of aging. Mechanisms of Ageing and Development, 222, 111991. https://doi.org/10.1016/j.mad.2024.111991spa
dc.identifier.doi10.1016/j.mad.2024.111991
dc.identifier.issn0047-6374
dc.identifier.issn1872-6216
dc.identifier.urihttp://hdl.handle.net/11268/13062
dc.language.isoengspa
dc.peerreviewedSispa
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0047637424000915spa
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.otherPremature aging, Brain, Behavior, Immune function, Redox state, Longevityspa
dc.subject.sdgGoal 3: Ensure healthy lives and promote well-being for all at all ages
dc.subject.unescoEnvejecimientospa
dc.subject.unescoCerebrospa
dc.subject.unescoInmunologíaspa
dc.titleCharacterization of a natural model of adult mice with different rate of agingspa
dc.typejournal articlespa
dspace.entity.typePublication

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