Cargando…

Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice

Sex differences in aging and longevity have been widely observed, with females consistently outliving males across human populations. However, the mechanisms driving these disparities remain poorly understood. In this study, we explored the influence of post‐pubertal testicular effects on sex differ...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Nisi, Cheng, Catherine J., Gelfond, Jonathan, Strong, Randy, Diaz, Vivian, Nelson, James F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410013/
https://www.ncbi.nlm.nih.gov/pubmed/37221997
http://dx.doi.org/10.1111/acel.13891
_version_ 1785086365043523584
author Jiang, Nisi
Cheng, Catherine J.
Gelfond, Jonathan
Strong, Randy
Diaz, Vivian
Nelson, James F.
author_facet Jiang, Nisi
Cheng, Catherine J.
Gelfond, Jonathan
Strong, Randy
Diaz, Vivian
Nelson, James F.
author_sort Jiang, Nisi
collection PubMed
description Sex differences in aging and longevity have been widely observed, with females consistently outliving males across human populations. However, the mechanisms driving these disparities remain poorly understood. In this study, we explored the influence of post‐pubertal testicular effects on sex differences in aging by prepubertally castrating genetically heterogeneous (UM‐HET3) mice, a unique mouse model that emulates human sex differences in age‐related mortality. Prepubertal castration eliminated the longevity disparity between sexes by reducing the elevated early‐ to mid‐life mortality rate observed in males and extending their median lifespan to match that of females. Additionally, castration extended the duration of body weight growth and attenuated the inverse correlation between early‐age body weight and lifespan in males, aligning their growth trajectories with those of females. Our findings suggest that post‐pubertal testicular actions in genetically diverse mice are primarily responsible for sex differences in longevity as well as growth trajectories. These findings offer a foundation for further investigation into the fundamental mechanisms driving sex‐specific aging patterns and the development of potential pro‐longevity interventions.
format Online
Article
Text
id pubmed-10410013
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-104100132023-08-10 Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice Jiang, Nisi Cheng, Catherine J. Gelfond, Jonathan Strong, Randy Diaz, Vivian Nelson, James F. Aging Cell Short Communications Sex differences in aging and longevity have been widely observed, with females consistently outliving males across human populations. However, the mechanisms driving these disparities remain poorly understood. In this study, we explored the influence of post‐pubertal testicular effects on sex differences in aging by prepubertally castrating genetically heterogeneous (UM‐HET3) mice, a unique mouse model that emulates human sex differences in age‐related mortality. Prepubertal castration eliminated the longevity disparity between sexes by reducing the elevated early‐ to mid‐life mortality rate observed in males and extending their median lifespan to match that of females. Additionally, castration extended the duration of body weight growth and attenuated the inverse correlation between early‐age body weight and lifespan in males, aligning their growth trajectories with those of females. Our findings suggest that post‐pubertal testicular actions in genetically diverse mice are primarily responsible for sex differences in longevity as well as growth trajectories. These findings offer a foundation for further investigation into the fundamental mechanisms driving sex‐specific aging patterns and the development of potential pro‐longevity interventions. John Wiley and Sons Inc. 2023-05-23 /pmc/articles/PMC10410013/ /pubmed/37221997 http://dx.doi.org/10.1111/acel.13891 Text en © 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Jiang, Nisi
Cheng, Catherine J.
Gelfond, Jonathan
Strong, Randy
Diaz, Vivian
Nelson, James F.
Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
title Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
title_full Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
title_fullStr Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
title_full_unstemmed Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
title_short Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
title_sort prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410013/
https://www.ncbi.nlm.nih.gov/pubmed/37221997
http://dx.doi.org/10.1111/acel.13891
work_keys_str_mv AT jiangnisi prepubertalcastrationeliminatessexdifferencesinlifespanandgrowthtrajectoriesingeneticallyheterogeneousmice
AT chengcatherinej prepubertalcastrationeliminatessexdifferencesinlifespanandgrowthtrajectoriesingeneticallyheterogeneousmice
AT gelfondjonathan prepubertalcastrationeliminatessexdifferencesinlifespanandgrowthtrajectoriesingeneticallyheterogeneousmice
AT strongrandy prepubertalcastrationeliminatessexdifferencesinlifespanandgrowthtrajectoriesingeneticallyheterogeneousmice
AT diazvivian prepubertalcastrationeliminatessexdifferencesinlifespanandgrowthtrajectoriesingeneticallyheterogeneousmice
AT nelsonjamesf prepubertalcastrationeliminatessexdifferencesinlifespanandgrowthtrajectoriesingeneticallyheterogeneousmice