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1
Prepubertal castration eliminates sex differences in lifespan and growth trajectories in genetically heterogeneous mice.青春期前去势消除了遗传异质性小鼠寿命和生长轨迹的性别差异。
Aging Cell. 2023 Aug;22(8):e13891. doi: 10.1111/acel.13891. Epub 2023 May 23.
2
The emerging role of extracellular vesicles in the testis.外泌体在睾丸中的新兴作用。
Hum Reprod. 2023 Mar 1;38(3):334-351. doi: 10.1093/humrep/dead015.
3
Sex- and age-dependent genetics of longevity in a heterogeneous mouse population.性别和年龄依赖性遗传与异质鼠群的长寿相关。
Science. 2022 Sep 30;377(6614):eabo3191. doi: 10.1126/science.abo3191.
4
Sex and gender: modifiers of health, disease, and medicine.性别与健康、疾病和医学。
Lancet. 2020 Aug 22;396(10250):565-582. doi: 10.1016/S0140-6736(20)31561-0.
5
Genetically heterogeneous mice exhibit a female survival advantage that is age- and site-specific: Results from a large multi-site study.基因异质性小鼠表现出一种雌性生存优势,这种优势具有年龄和部位特异性:一项大型多中心研究的结果。
Aging Cell. 2019 Jun;18(3):e12905. doi: 10.1111/acel.12905. Epub 2019 Feb 23.
6
NIA Interventions Testing Program: Investigating Putative Aging Intervention Agents in a Genetically Heterogeneous Mouse Model.美国国立衰老研究所干预测试项目:在基因异质性小鼠模型中研究假定的衰老干预剂。
EBioMedicine. 2017 Jul;21:3-4. doi: 10.1016/j.ebiom.2016.11.038. Epub 2016 Dec 2.
7
No Ground for Advocating that Korean Eunuchs Lived Longer than Intact Men.没有理由主张韩国太监比正常男性寿命更长。
Gerontology. 2015;62(1):69-70. doi: 10.1159/000435854. Epub 2015 Jun 30.
8
Adverse effects of androgen deprivation therapy and strategies to mitigate them.雄激素剥夺治疗的不良反应及其缓解策略。
Eur Urol. 2015 May;67(5):825-36. doi: 10.1016/j.eururo.2014.07.010. Epub 2014 Aug 2.
9
Nordihydroguaiaretic acid and aspirin increase lifespan of genetically heterogeneous male mice.去甲二氢愈创木酸和阿司匹林可延长基因异质雄性小鼠的寿命。
Aging Cell. 2008 Oct;7(5):641-50. doi: 10.1111/j.1474-9726.2008.00414.x.
10
Organizational and activational effects of sex steroids on brain and behavior: a reanalysis.性类固醇对大脑和行为的组织及激活作用:重新分析
Horm Behav. 1985 Dec;19(4):469-98. doi: 10.1016/0018-506x(85)90042-x.

去势降低雄性小鼠的死亡率并增加其适应力:下一步是什么?

Castration reduces mortality and increases resilience in male mice: what is next?

机构信息

The Sam and Ann Barshop Institute for Longevity and Aging Studies, UT Health San Antonio, San Antonio, TX, USA.

Department of Cellular and Integrative Physiology, UT Health San Antonio, San Antonio, TX, USA.

出版信息

Geroscience. 2024 Apr;46(2):2787-2790. doi: 10.1007/s11357-023-00973-5. Epub 2023 Oct 20.

DOI:10.1007/s11357-023-00973-5
PMID:37861928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10828236/
Abstract

This commentary concerns our recent report that prepubertal castration rescued the shorter lifespan of males, using the first mouse line that robustly shows the same shorter longevity with a similar age-variable mortality disadvantage as human males. This model provides a unique opportunity for research to uncover the basis for this clinically important sex difference in aging. Researchers can now identify the hormones involved, the duration of exposure required, and, most important, the cellular and molecular targets, with the ultimate goal of developing therapeutic interventions to enhance health and reduce mortality without castration-compromising reproductive function.

摘要

这篇评论是关于我们最近的一项报告,该报告指出,青春期前去势可以挽救雄性的寿命缩短,我们使用了第一条强有力地显示出与人类男性相似的寿命缩短和相似的年龄相关死亡率劣势的老鼠模型。该模型为研究提供了一个独特的机会,可以揭示这种临床上重要的性别差异在衰老中的基础。研究人员现在可以确定涉及的激素、所需的暴露时间,最重要的是,细胞和分子靶点,最终目标是开发治疗干预措施,在不损害生殖功能的情况下,增强健康并降低死亡率。