• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

衰老会停止吗?

Does aging stop?

作者信息

Shahrestani Parvin, Mueller Laurence D, Rose Michael R

机构信息

Department of Ecology and Evolutionary Biology, University of California, Irvine, California 92697-2525, USA.

出版信息

Curr Aging Sci. 2009 Mar;2(1):3-11. doi: 10.2174/1874609810902010003.

DOI:10.2174/1874609810902010003
PMID:20021395
Abstract

Human mortality data show stabilization in mortality rates at very late ages. But human mortality data are difficult to interpret because they are affected by changing medical practices and other historically variable causes of death. However, in the 1990s, data from a variety of labs showed that the mortality rates of medflies, fruit flies, wasps, yeasts, and nematodes also stabilize at very late ages. These reproducible "mortality-rate plateaus" forced biologists to develop theories for their existence. There are two main theories of this kind. "Lifelong heterogeneity" theories suppose that highly robust subcohorts are more abundant at later ages because less robust subcohorts have mostly died off. On this type of theory, aging does not stop; aging continues inexorably in all individuals. In contrast, in evolutionary theories for mortality-rate plateaus, based on the eventual plateaus in Hamilton's Forces of Natural Selection at late ages, aging does indeed stop. A variety of experiments have cast doubt on lifelong heterogeneity theories as explanations of mortality-rate plateaus. A few experiments have corroborated the Hamiltonian theory. This has the important corollary that it appears to be possible for aging to stop, at sufficiently late ages, at least among some populations. The implications of this result for aging research are profound. Most importantly, it suggests the possibility that the physiology of adults undergoing aging may be substantially different from the physiology of life after aging.

摘要

人类死亡率数据显示,在高龄阶段死亡率趋于稳定。但人类死亡率数据难以解读,因为它们受到医疗实践变化及其他历史上可变的死亡原因影响。然而,在20世纪90年代,来自多个实验室的数据表明,地中海果蝇、果蝇、黄蜂、酵母和线虫的死亡率在高龄阶段也会稳定下来。这些可重复的“死亡率平台期”促使生物学家为其存在提出理论。这类理论主要有两种。“终生异质性”理论认为,高度强健的亚群体在晚年更为丰富,因为较弱健的亚群体大多已经死亡。在这类理论中,衰老不会停止;衰老在所有个体中无情地持续。相比之下,在死亡率平台期的进化理论中,基于汉密尔顿自然选择力在晚年最终达到平台期,衰老确实会停止。一系列实验对将终生异质性理论作为死亡率平台期的解释提出了质疑。一些实验证实了哈密顿理论。这有一个重要的推论,即至少在某些群体中,衰老在足够晚的年龄似乎有可能停止。这一结果对衰老研究的影响意义深远。最重要的是,它表明正在衰老的成年人的生理学可能与衰老后的生命生理学有很大不同。

相似文献

1
Does aging stop?衰老会停止吗?
Curr Aging Sci. 2009 Mar;2(1):3-11. doi: 10.2174/1874609810902010003.
2
A revolution for aging research.衰老研究的一场革命。
Biogerontology. 2006 Aug;7(4):269-77. doi: 10.1007/s10522-006-9001-6. Epub 2006 Apr 13.
3
Late life: a new frontier for physiology.晚年:生理学的新前沿。
Physiol Biochem Zool. 2005 Nov-Dec;78(6):869-78. doi: 10.1086/498179. Epub 2005 Oct 13.
4
Hamilton's forces of natural selection after forty years.四十年后的汉密尔顿自然选择力量
Evolution. 2007 Jun;61(6):1265-76. doi: 10.1111/j.1558-5646.2007.00120.x.
5
Why ageing stops: heterogeneity explains late-life mortality deceleration in nematodes.衰老为何停止:异质性解释线虫晚年死亡率减缓。
Biol Lett. 2013 Oct 2;9(5):20130217. doi: 10.1098/rsbl.2013.0217. Print 2013 Oct 23.
6
Ageing and immortality.衰老与不朽
Philos Trans R Soc Lond B Biol Sci. 2000 Nov 29;355(1403):1657-62. doi: 10.1098/rstb.2000.0728.
7
Mortality plateaus and directionality theory.死亡率平稳期与方向性理论。
Proc Biol Sci. 2001 Oct 7;268(1480):2029-37. doi: 10.1098/rspb.2001.1739.
8
The evolution of late life.晚年的演变。
Ageing Res Rev. 2006 Feb;5(1):14-32. doi: 10.1016/j.arr.2005.06.003. Epub 2005 Aug 8.
9
Aging in the context of cohort evolution and mortality selection.从队列演变和死亡率选择的角度看衰老。
Demography. 2014 Aug;51(4):1295-317. doi: 10.1007/s13524-014-0306-9.
10
Lifelong heterogeneity in fecundity is insufficient to explain late-life fecundity plateaus in Drosophila melanogaster.生育力的终身异质性不足以解释黑腹果蝇晚年生育力的平稳状态。
Exp Gerontol. 2005 Aug-Sep;40(8-9):660-70. doi: 10.1016/j.exger.2005.06.006.

引用本文的文献

1
The African killifish: A short-lived vertebrate model to study the biology of sarcopenia and longevity.非洲食蚊鱼:一种寿命较短的脊椎动物模型,可用于研究肌肉减少症和长寿的生物学。
Aging Cell. 2024 Jan;23(1):e13862. doi: 10.1111/acel.13862. Epub 2023 May 14.
2
Herbal supplement extends life span under some environmental conditions and boosts stress resistance.草药补充剂在某些环境条件下可延长寿命并增强抗应激能力。
PLoS One. 2015 Apr 16;10(4):e0119068. doi: 10.1371/journal.pone.0119068. eCollection 2015.
3
Worker senescence and the sociobiology of aging in ants.
工蚁衰老与蚂蚁衰老的社会生物学
Behav Ecol Sociobiol. 2014 Dec;68(12):1901-1919. doi: 10.1007/s00265-014-1826-4.
4
What is Aging?什么是衰老?
Front Genet. 2012 Jul 20;3:134. doi: 10.3389/fgene.2012.00134. eCollection 2012.
5
Nicotinamide, NAD(P)(H), and Methyl-Group Homeostasis Evolved and Became a Determinant of Ageing Diseases: Hypotheses and Lessons from Pellagra.烟酰胺、NAD(P)(H)与甲基基团稳态的演变及其成为衰老相关疾病的决定因素:来自糙皮病的假说与启示
Curr Gerontol Geriatr Res. 2012;2012:302875. doi: 10.1155/2012/302875. Epub 2012 Mar 21.
6
Paradoxical physiological transitions from aging to late life in Drosophila.果蝇从衰老到老年的矛盾性生理转变。
Rejuvenation Res. 2012 Feb;15(1):49-58. doi: 10.1089/rej.2011.1201. Epub 2012 Jan 10.
7
Mitochondrial changes in ageing Caenorhabditis elegans--what do we learn from superoxide dismutase knockouts?衰老的秀丽隐杆线虫中线粒体的变化——超氧化物歧化酶敲除能告诉我们什么?
PLoS One. 2011;6(5):e19444. doi: 10.1371/journal.pone.0019444. Epub 2011 May 18.
8
Biology of the Mi-2/NuRD Complex in SLAC (Stemness, Longevity/Ageing, and Cancer).SLAC(干性、长寿/衰老和癌症)中Mi-2/NuRD复合物的生物学特性
Gene Regul Syst Bio. 2011 Feb 27;5:1-26. doi: 10.4137/GRSB.S6510.