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Is an MRI-derived anatomical measure of dementia risk also a measure of brain aging?MRI 衍生的痴呆风险解剖学测量指标是否也是大脑老化的测量指标?
Geroscience. 2023 Feb;45(1):439-450. doi: 10.1007/s11357-022-00650-z. Epub 2022 Sep 2.
3
A Neuroscience Primer for Integrating Geroscience With the Neurobiology of Aging.衰老神经科学与神经生物学整合的神经科学基础
J Gerontol A Biol Sci Med Sci. 2022 Jan 7;77(1):e19-e33. doi: 10.1093/gerona/glab301.

本文引用的文献

1
A Neuroscience Primer for Integrating Geroscience With the Neurobiology of Aging.衰老神经科学与神经生物学整合的神经科学基础
J Gerontol A Biol Sci Med Sci. 2022 Jan 7;77(1):e19-e33. doi: 10.1093/gerona/glab301.
2
Reuniting the Body "Neck Up and Neck Down" to Understand Cognitive Aging: The Nexus of Geroscience and Neuroscience.将身体“颈部以上与颈部以下”重新结合以理解认知衰老:老年科学与神经科学的关联
J Gerontol A Biol Sci Med Sci. 2022 Jan 7;77(1):e1-e9. doi: 10.1093/gerona/glab215.
3
The hoverfly and the wasp: A critique of the hallmarks of aging as a paradigm.食蚜蝇与黄蜂:对衰老作为范式的标志性特征的批判。
Ageing Res Rev. 2021 Sep;70:101407. doi: 10.1016/j.arr.2021.101407. Epub 2021 Jul 13.
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Octodon degus: a natural model of multimorbidity for ageing research.八齿鼠:衰老研究中多种共病的自然模型。
Ageing Res Rev. 2020 Dec;64:101204. doi: 10.1016/j.arr.2020.101204. Epub 2020 Nov 2.
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Effects of caloric restriction on human physiological, psychological, and behavioral outcomes: highlights from CALERIE phase 2.热量限制对人类生理、心理和行为结果的影响:CALERIE 阶段 2 的重点。
Nutr Rev. 2021 Jan 1;79(1):98-113. doi: 10.1093/nutrit/nuaa085.
6
Age and life expectancy clocks based on machine learning analysis of mouse frailty.基于机器学习分析小鼠脆弱性的年龄和预期寿命时钟。
Nat Commun. 2020 Sep 15;11(1):4618. doi: 10.1038/s41467-020-18446-0.
7
Blood factors transfer beneficial effects of exercise on neurogenesis and cognition to the aged brain.血液因素将运动对神经发生和认知的有益影响转移到老年大脑。
Science. 2020 Jul 10;369(6500):167-173. doi: 10.1126/science.aaw2622.
8
Challenging a "Cushy" Life: Potential Roles of Thermogenesis and Adipose Tissue Adaptations in Delayed Aging of Ames and Snell Dwarf Mice.挑战“舒适”生活:产热和脂肪组织适应性在艾姆斯和斯内尔侏儒小鼠延缓衰老中的潜在作用
Metabolites. 2020 Apr 29;10(5):176. doi: 10.3390/metabo10050176.
9
Age influences domestic dog cognitive performance independent of average breed lifespan.年龄独立于平均品种寿命影响家犬认知表现。
Anim Cogn. 2020 Jul;23(4):795-805. doi: 10.1007/s10071-020-01385-0. Epub 2020 Apr 30.
10
Understanding the Physiological Links Between Physical Frailty and Cognitive Decline.理解身体虚弱与认知衰退之间的生理联系。
Aging Dis. 2020 Mar 9;11(2):405-418. doi: 10.14336/AD.2019.0521. eCollection 2020 Apr.

弥合差距:神经科学家的衰老科学入门及其潜在的合作应用。

Bridging the Gap: A Geroscience Primer for Neuroscientists With Potential Collaborative Applications.

机构信息

Department of Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Department of Cellular, Development, and Integrative Biology, The University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2022 Jan 7;77(1):e10-e18. doi: 10.1093/gerona/glab314.

DOI:10.1093/gerona/glab314
PMID:34653247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8751800/
Abstract

While neurodegenerative diseases can strike at any age, the majority of afflicted individuals are diagnosed at older ages. Due to the important impact of age in disease diagnosis, the field of neuroscience could greatly benefit from the many of the theories and ideas from the biology of aging-now commonly referred as geroscience. As discussed in our complementary perspective on the topic, there is often a "silo-ing" between geroscientists who work on understanding the mechanisms underlying aging and neuroscientists who are studying neurodegenerative diseases. While there have been some strong collaborations between the biology of aging and neuroscientists, there is still great potential for enhanced collaborative effort between the 2 fields. To this end, here, we review the state of the geroscience field, discuss how neuroscience could benefit from thinking from a geroscience perspective, and close with a brief discussion on some of the "missing links" between geroscience and neuroscience and how to remedy them. Notably, we have a corresponding, concurrent review from the neuroscience perspective. Our overall goal is to "bridge the gap" between geroscience and neuroscience such that more efficient, reproducible research with translational potential can be conducted.

摘要

虽然神经退行性疾病可能在任何年龄发作,但大多数受影响的个体都是在老年时被诊断出来的。由于年龄在疾病诊断中的重要影响,神经科学领域可以从衰老生物学的许多理论和观点中受益匪浅——现在通常被称为衰老科学。正如我们在关于该主题的补充观点中所讨论的,研究衰老机制的衰老科学家和研究神经退行性疾病的神经科学家之间经常存在“筒仓”现象。虽然衰老生物学和神经科学家之间已经有了一些强有力的合作,但这两个领域之间仍有很大的潜力进行更加强化的合作。为此,在这里,我们回顾了衰老科学领域的现状,讨论了神经科学如何从衰老科学的角度受益,并简要讨论了衰老科学和神经科学之间的一些“缺失环节”以及如何弥补这些环节。值得注意的是,我们有一个来自神经科学角度的相应的、同时进行的综述。我们的总体目标是在衰老科学和神经科学之间“架起桥梁”,以便能够进行更高效、更可重复且具有转化潜力的研究。