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衰老——是什么以及如何衡量它。

Aging - What it is and how to measure it.

机构信息

Translational Biogerontology Lab, German Center for Neurodegenerative Diseases (DZNE), Venusberg-Campus 1, 53127 Bonn, Germany.

Aging and Neurodegeneration Lab, German Center for Neurodegenerative Diseases (DZNE), Venusberg-Campus 1, 53127 Bonn, Germany.

出版信息

Mech Ageing Dev. 2023 Jul;213:111837. doi: 10.1016/j.mad.2023.111837. Epub 2023 Jun 9.

Abstract

The current understanding of the biology of aging is largely based on research aimed at identifying factors that influence lifespan. However, lifespan as a sole proxy measure of aging has limitations because it can be influenced by specific pathologies (not generalized physiological deterioration in old age). Hence, there is a great need to discuss and design experimental approaches that are well-suited for studies targeting the biology of aging, rather than the biology of specific pathologies that restrict the lifespan of a given species. For this purpose, we here review various perspectives on aging, discuss agreement and disagreement among researchers on the definition of aging, and show that while slightly different aspects are emphasized, a widely accepted feature, shared across many definitions, is that aging is accompanied by phenotypic changes that occur in a population over the course of an average lifespan. We then discuss experimental approaches that are in line with these considerations, including multidimensional analytical frameworks as well as designs that facilitate the proper assessment of intervention effects on aging rate. The proposed framework can guide discovery approaches to aging mechanisms in all key model organisms (e.g., mouse, fish models, D. melanogaster, C. elegans) as well as in humans.

摘要

目前对衰老生物学的理解在很大程度上是基于旨在识别影响寿命的因素的研究。然而,寿命作为衰老的唯一代理衡量标准存在局限性,因为它可能受到特定病理的影响(而不是老年时普遍的生理恶化)。因此,非常有必要讨论和设计适合研究衰老生物学的实验方法,而不是针对特定病理的生物学方法,这些方法会限制特定物种的寿命。为此,我们在这里回顾了衰老的各种观点,讨论了研究人员在衰老定义上的一致性和分歧,并表明虽然强调的方面略有不同,但一个被广泛接受的特征是,衰老伴随着表型变化,这些变化在一个种群中平均寿命内发生。然后,我们讨论了符合这些考虑因素的实验方法,包括多维分析框架以及便于适当评估干预对衰老速度影响的设计。所提出的框架可以指导所有关键模型生物(例如,老鼠、鱼类模型、D. melanogaster、C. elegans)以及人类的衰老机制的发现方法。

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