Telomeres and the Rate of Living: Linking Biological Clocks of Senescence.

Ecological and evolutionary physiology Pub Date : 2024-05-01 Epub Date: 2024-05-15 DOI:10.1086/730588
James F Gillooly, Emily S Khazan
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Abstract

AbstractTwo prominent theories of aging, one based on telomere dynamics and the other on mass-specific energy flux, propose biological time clocks of senescence. The relationship between these two theories, and the biological clocks proposed by each, remains unclear. Here, we examine the relationships between telomere shortening rate, mass-specific metabolic rate, and lifespan among vertebrates (mammals, birds, fishes). Results show that telomere shortening rate increases linearly with mass-specific metabolic rate and decreases nonlinearly with increasing body mass in the same way as mass-specific metabolic rate. Results also show that both telomere shortening rate and mass-specific metabolic rate are similarly related to lifespan and that both strongly predict differences in lifespan, although the slopes of the relationships are less than linear. On average, then, telomeres shorten a fixed amount per unit of mass-specific energy flux. So the mitotic clock of telomere shortening and the energetics-based clock described by metabolic rate can be viewed as alternative measures of the same biological clock. These two processes may be linked, we speculate, through the process of cell division.

端粒与生活节奏:连接衰老的生物钟。
摘要两种著名的衰老理论,一种以端粒动力学为基础,另一种以质量特异性能量通量为基础,提出了衰老的生物钟。这两种理论和各自提出的生物钟之间的关系仍不清楚。在这里,我们研究了脊椎动物(哺乳动物、鸟类和鱼类)端粒缩短率、质量特异性代谢率和寿命之间的关系。结果表明,端粒缩短率与质量特异性代谢率呈线性增长,与质量特异性代谢率一样,随着体重的增加呈非线性下降。结果还显示,端粒缩短率和质量特异性代谢率与寿命的关系类似,都能强烈预测寿命的差异,尽管两者关系的斜率不是线性的。因此,平均而言,每单位质量的特定能量通量会使端粒缩短一个固定的数量。因此,端粒缩短的有丝分裂时钟和新陈代谢率所描述的基于能量的时钟可以被看作是同一生物钟的替代措施。我们推测,这两个过程可能通过细胞分裂过程联系在一起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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