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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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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 |
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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 |
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