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热量限制:近期研究结果对衰老研究未来的启示。

Calorie restriction: what recent results suggest for the future of ageing research.

机构信息

Department of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Eur J Clin Invest. 2010 May;40(5):440-50. doi: 10.1111/j.1365-2362.2010.02276.x.


DOI:10.1111/j.1365-2362.2010.02276.x
PMID:20534066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3073505/
Abstract

BACKGROUND: Calorie Restriction (CR) research has expanded rapidly over the past few decades and CR remains the most highly reproducible, environmental intervention to improve health and extend lifespan in animal studies. Although many model organisms have consistently demonstrated positive responses to CR, it remains to be shown whether CR will extend lifespan in humans. Additionally, the current environment of excess caloric consumption and high incidence of overweight/obesity illustrate the improbable nature of the long-term adoption of a CR lifestyle by a significant proportion of the human population. Thus, the search for substances that can reproduce the beneficial physiologic responses of CR without a requisite calorie intake reduction, termed CR mimetics (CRMs), has gained momentum. MATERIAL AND METHODS: Recent articles describing health and lifespan results of CR in nonhuman primates and short-term human studies are discussed. Additional consideration is given to the rapidly expanding search for CRMs. RESULTS: The first results from a long-term, randomized, controlled CR study in nonhuman primates showing statistically significant benefits on longevity have now been reported. Additionally, positive results from short-term, randomized, controlled CR studies in humans are suggestive of potential health and longevity gains, while test of proposed CRMs (including rapamycin, resveratrol, 2-deoxyglucose and metformin) have shown both positive and mixed results in rodents. CONCLUSION: Whether current positive results will translate into longevity gains for humans remains an open question. However, the apparent health benefits that have been observed with CR suggest that regardless of longevity gains, the promotion of healthy ageing and disease prevention may be attainable.

摘要

背景:在过去几十年中,热量限制(CR)研究迅速发展,CR 仍然是改善健康和延长动物研究寿命最具可重复性的环境干预措施。尽管许多模式生物一致显示出对 CR 的积极反应,但 CR 是否会延长人类寿命仍有待证明。此外,当前过量卡路里摄入和超重/肥胖发病率高的环境表明,人类的很大一部分长期采用 CR 生活方式是不太可能的。因此,寻找能够在不减少热量摄入的情况下复制 CR 有益生理反应的物质,称为 CR 模拟物(CRMs),已经引起了关注。

材料和方法:讨论了描述非人类灵长类动物 CR 对健康和寿命影响的最新文章和短期人类研究。还对迅速扩大的 CRM 搜索进行了额外的考虑。

结果:现在已经报道了第一项在非人类灵长类动物中进行的长期、随机、对照 CR 研究的结果,该研究显示在长寿方面具有统计学意义的益处。此外,短期、随机、对照 CR 研究在人类中取得的积极结果表明,可能会带来健康和长寿的收益,而对拟议的 CRMs(包括雷帕霉素、白藜芦醇、2-脱氧葡萄糖和二甲双胍)的测试在啮齿动物中显示出了积极和混合的结果。

结论:目前的积极结果是否会转化为人类的长寿收益仍是一个悬而未决的问题。然而,CR 观察到的明显健康益处表明,无论是否能延长寿命,促进健康衰老和预防疾病可能是可以实现的。

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本文引用的文献

[1]
Metformin induces a dietary restriction-like state and the oxidative stress response to extend C. elegans Healthspan via AMPK, LKB1, and SKN-1.

PLoS One. 2010-1-18

[2]
SRT1720, SRT2183, SRT1460, and resveratrol are not direct activators of SIRT1.

J Biol Chem. 2010-1-8

[3]
Chronic ingestion of 2-deoxy-D-glucose induces cardiac vacuolization and increases mortality in rats.

Toxicol Appl Pharmacol. 2009-12-22

[4]
Resveratrol is not a direct activator of SIRT1 enzyme activity.

Chem Biol Drug Des. 2009-10-20

[5]
Ageing populations: the challenges ahead.

Lancet. 2009-10-3

[6]
Calorie restriction reduces rDNA recombination independently of rDNA silencing.

Aging Cell. 2009-9-2

[7]
Calorie restriction effects on silencing and recombination at the yeast rDNA.

Aging Cell. 2009-9-2

[8]
Biomarkers of aging and disease: introduction and definitions.

Exp Gerontol. 2009-8-3

[9]
Caloric restriction delays disease onset and mortality in rhesus monkeys.

Science. 2009-7-10

[10]
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice.

Nature. 2009-7-16

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