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关于寿命相关性中的因果联系以及分子水平上“生命数量”的可能存在。

On the causal connection in lifespan correlations and the possible existence of a 'number of life' at molecular level.

作者信息

Escala Andrés

机构信息

Departamento de Astronomía, Universidad de Chile, Casilla 36-D, Santiago, Chile.

出版信息

Sci Rep. 2024 Dec 30;14(1):31707. doi: 10.1038/s41598-024-82671-6.

DOI:10.1038/s41598-024-82671-6
PMID:39738314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11685859/
Abstract

Multiple physiological traits correlates with lifespan, being unclear both the causal connection among them and with the process of ageing. In this paper, we show that six traits (such as metabolic rate, mass, heart rate, etc) acting at the system level, are all related to lifespan thru the existence of an approximately constant number of respiration cycles in a lifespan ([Formula: see text]), therefore, we find that those relationships are not independently related to ageing. In addition, we study if the approximately constant [Formula: see text] is possibly linked with the end-of-lifespan somatic mutation burden, another number recently found to be approximately constant (Cagan, Nature 604:517-524, 2022). We find that the dataset of mammals studied is consistent with a direct proportionality between the somatic mutation rate and the respiration frequency, being a tentative link between both invariant numbers.

摘要

多种生理特征与寿命相关,它们之间的因果关系以及与衰老过程的关系都尚不清楚。在本文中,我们表明在系统水平上起作用的六个特征(如代谢率、体重、心率等),通过寿命中存在大致恒定数量的呼吸周期([公式:见正文])都与寿命相关,因此,我们发现这些关系并非独立于衰老相关。此外,我们研究了大致恒定的[公式:见正文]是否可能与寿命末期体细胞突变负担相关,体细胞突变负担是最近发现的另一个大致恒定的数值(卡根,《自然》604:517 - 524,2022)。我们发现所研究的哺乳动物数据集与体细胞突变率和呼吸频率之间的直接比例关系一致,这是这两个不变数值之间的一种初步联系。

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1
On the causal connection in lifespan correlations and the possible existence of a 'number of life' at molecular level.关于寿命相关性中的因果联系以及分子水平上“生命数量”的可能存在。
Sci Rep. 2024 Dec 30;14(1):31707. doi: 10.1038/s41598-024-82671-6.
2
The impact of the cardiovascular component and somatic mutations on ageing.心血管成分和体细胞突变对衰老的影响。
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本文引用的文献

1
The impact of the cardiovascular component and somatic mutations on ageing.心血管成分和体细胞突变对衰老的影响。
Aging Cell. 2023 Oct;22(10):e13957. doi: 10.1111/acel.13957. Epub 2023 Aug 22.
2
Naked Mole-Rats Demonstrate Profound Tolerance to Low Oxygen, High Carbon Dioxide, and Chemical Pain.裸鼹鼠对低氧、高二氧化碳和化学疼痛表现出极强的耐受性。
Animals (Basel). 2023 Feb 24;13(5):819. doi: 10.3390/ani13050819.
3
Somatic mutation rates scale with lifespan across mammals.哺乳动物的体细胞突变率与寿命成正比。
Nature. 2022 Apr;604(7906):517-524. doi: 10.1038/s41586-022-04618-z. Epub 2022 Apr 13.
4
Universal relation for life-span energy consumption in living organisms: Insights for the origin of aging.生物体寿命能量消耗的普遍关系:衰老起源的新见解。
Sci Rep. 2022 Feb 21;12(1):2407. doi: 10.1038/s41598-022-06390-6.
5
[Key Molecular Mechanisms of Aging, Biomarkers, and Potential Interventions].[衰老的关键分子机制、生物标志物及潜在干预措施]
Mol Biol (Mosk). 2020 Nov-Dec;54(6):883-921. doi: 10.31857/S0026898420060099.
6
Naked Mole-Rat mortality rates defy gompertzian laws by not increasing with age.裸鼹鼠的死亡率与冈珀茨定律相悖,并不会随着年龄的增长而增加。
Elife. 2018 Jan 24;7:e31157. doi: 10.7554/eLife.31157.
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The hallmarks of aging.衰老的特征。
Cell. 2013 Jun 6;153(6):1194-217. doi: 10.1016/j.cell.2013.05.039.
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Curvature in metabolic scaling.代谢缩放中的曲率。
Nature. 2010 Apr 1;464(7289):753-6. doi: 10.1038/nature08920.
9
Revisiting a model of ontogenetic growth: estimating model parameters from theory and data.重新审视个体发育生长模型:从理论和数据估计模型参数。
Am Nat. 2008 May;171(5):632-45. doi: 10.1086/587073.
10
Life and death: metabolic rate, membrane composition, and life span of animals.生与死:动物的代谢率、膜组成与寿命
Physiol Rev. 2007 Oct;87(4):1175-213. doi: 10.1152/physrev.00047.2006.