Characterization of a natural model of adult mice with different rate of aging
| dc.contributor.author | Félix, Judith | |
| dc.contributor.author | Díaz del Cerro, Estefanía | |
| dc.contributor.author | Garrido Garrío, Antonio | |
| dc.contributor.author | Fuente, Mónica de la | |
| dc.date.accessioned | 2024-09-21T11:07:14Z | |
| dc.date.available | 2024-09-21T11:07:14Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | Aging 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.filiation | UEM | spa |
| dc.description.impact | 5.3 Q2 JCR 2023 | spa |
| dc.description.impact | 1.577 Q1 SJR 2023 | spa |
| dc.description.impact | No data IDR 2023 | spa |
| dc.description.sponsorship | This research was funded by the Research Group UCM ( 910379 ). | spa |
| dc.identifier.citation | Félix, 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.2024.111991 | spa |
| dc.identifier.doi | 10.1016/j.mad.2024.111991 | |
| dc.identifier.issn | 0047-6374 | |
| dc.identifier.issn | 1872-6216 | |
| dc.identifier.uri | http://hdl.handle.net/11268/13062 | |
| dc.language.iso | eng | spa |
| dc.peerreviewed | Si | spa |
| dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0047637424000915 | spa |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.accessRights | open access | spa |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject.other | Premature aging, Brain, Behavior, Immune function, Redox state, Longevity | spa |
| dc.subject.sdg | Goal 3: Ensure healthy lives and promote well-being for all at all ages | |
| dc.subject.unesco | Envejecimiento | spa |
| dc.subject.unesco | Cerebro | spa |
| dc.subject.unesco | Inmunología | spa |
| dc.title | Characterization of a natural model of adult mice with different rate of aging | spa |
| dc.type | journal article | spa |
| dspace.entity.type | Publication |
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