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反应规范在饮食限制与衰老研究中的重要性。

The importance of reaction norms in dietary restriction and ageing research.

机构信息

School of Biosciences, University of Sheffield, Western Bank S10 2TN, UK.

School of Molecular Biosciences, University of Glasgow, G12 8QQ, UK.

出版信息

Ageing Res Rev. 2023 Jun;87:101926. doi: 10.1016/j.arr.2023.101926. Epub 2023 Apr 4.

DOI:10.1016/j.arr.2023.101926
PMID:37019387
Abstract

Ageing research has progressed rapidly through our ability to modulate the ageing process. Pharmacological and dietary treatments can increase lifespan and have been instrumental in our understanding of the mechanisms of ageing. Recently, several studies have reported genetic variance in response to these anti-ageing interventions, questioning their universal application and making a case for personalised medicine in our field. As an extension of these findings the response to dietary restriction was found to not be repeatable when the same genetic mouse lines were retested. We show here that this effect is more widespread with the response to dietary restriction also showing low repeatability across genetic lines in the fly (Drosophila melanogaster). We further argue that variation in reaction norms, the relationship between dose and response, can explain such conflicting findings in our field. We simulate genetic variance in reaction norms and show that such variation can: 1) lead to over- or under-estimation of treatment responses, 2) dampen the response measured if a genetically heterogeneous population is studied, and 3) illustrate that genotype-by-dose-by-environment interactions can lead to low repeatability of DR and potentially other anti-ageing interventions. We suggest that putting experimental biology and personalised geroscience in a reaction norm framework will aid progress in ageing research.

摘要

衰老研究通过我们调节衰老过程的能力取得了快速进展。药理学和饮食疗法可以延长寿命,并有助于我们理解衰老的机制。最近,有几项研究报告了对这些抗衰老干预措施的遗传变异反应,质疑它们的普遍适用性,并为我们领域的个性化医学提出了案例。作为这些发现的延伸,当相同的基因小鼠系被重新测试时,发现饮食限制的反应不能重复。我们在这里表明,这种效应更为普遍,在果蝇(Drosophila melanogaster)中,饮食限制的反应也表现出遗传系之间的低重复性。我们进一步认为,反应规范的变异,即剂量与反应之间的关系,可以解释我们领域中这些相互矛盾的发现。我们模拟了反应规范中的遗传方差,并表明这种变异可能导致:1)对治疗反应的高估或低估,2)如果研究具有遗传异质性的群体,则会抑制所测量的反应,3)说明基因型-剂量-环境相互作用可能导致 DR 和潜在的其他抗衰老干预措施的低重复性。我们建议将实验生物学和个性化衰老科学置于反应规范框架中,将有助于衰老研究的进展。

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