Evidence map›Paper›PMID 41238986›Full record

ArticleBiogerontology2025

Sex differences in behavior, immune function, and redox state throughout life, and their effect on the longevity of Swiss mice.

Judith Félix, Antonio Garrido, Mónica De la Fuente

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Article in Biogerontology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Judith FélixDepartment of Genetics, Physiology and Microbiology. School of Biology, Complutense University of Madrid, 28040, Madrid, Spain.ORCID 0000-0003-3319-7623
Antonio GarridoInstitute of Investigation Hospital 12 de Octubre (i+12), Hospital 12 de Octubre, 28041, Madrid, Spain. antonio.garrido@universidadeuropea.es.ORCID 0000-0003-3026-3330
Mónica De la FuenteDepartment of Genetics, Physiology and Microbiology. School of Biology, Complutense University of Madrid, 28040, Madrid, Spain.ORCID 0000-0002-5969-097X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homeostatic systems (nervous, immune, and endocrine) are crucial for maintaining health throughout life and, consequently, relevant for the rate of aging and the longevity achieved. In many species, male and female mammals show different lifespans, attributed to distinct redox states, but it is scarcely known whether sex differences in the functioning of these systems are involved. This study investigated, in an integrative view, sex differences in the nervous and immune systems of Swiss strain mice by analyzing behavior, immune function, and redox biomarkers across aging, to determine whether possible sex differences in homeostatic systems affect longevity. A longitudinal study was conducted on 20 female and male Swiss mice. At their young (2 mon), adult (7 mon), and old (18 mon) ages, subjects were subjected to a battery of behavioral tests, and peritoneal leukocytes were extracted to assess immune function and redox biomarkers. The natural deaths of animals were recorded for a longevity study. Our results indicate that sexual differences begin at a young age, and several are maintained until old age. Females, in general, show better behavior, immune function, and redox biomarkers, contributing to their higher longevity compared to males. The enhanced longevity in females may be attributable, in part, to the preservation of robust immune competence, with emphasis on innate immune functions and lower oxidative stress. The integration of behavioral and immunological profiles, together with redox biomarkers, underscores the critical importance of incorporating both sex as a biological variable in the design of aging-related research.

Indexed as

AgingBehavior, AnimalImmune SystemLongevitySex CharacteristicsAge FactorsAnimalsBiomarkersFemaleImmunity, InnateMaleMiceOxidation-ReductionOxidative StressSex FactorsBiomarkersAgingBehaviorImmunologyLongevityRedox stateSex differences

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.