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啮齿动物和非人类灵长类动物研究中的热量限制研究设计局限性

Caloric Restriction Study Design Limitations in Rodent and Nonhuman Primate Studies.

作者信息

Vaughan Kelli L, Kaiser Tamzin, Peaden Robert, Anson R Michael, de Cabo Rafael, Mattison Julie A

机构信息

Translational Gerontology Branch, National Institute on Aging, Dickerson, Maryland.

SoBran BioSciences, SoBran Inc., Burtonsville, Maryland.

出版信息

J Gerontol A Biol Sci Med Sci. 2017 Dec 12;73(1):48-53. doi: 10.1093/gerona/glx088.


DOI:10.1093/gerona/glx088
PMID:28977341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5861872/
Abstract

For a century, we have known that caloric restriction influences aging in many species. However, only recently it was firmly established that the effect is not entirely dependent on the calories provided. Instead, rodent and nonhuman primate models have shown that the rate of aging depends on other variables, including the macronutrient composition of the diet, the amount of time spent in the restricted state, age of onset, the gender and genetic background, and the particular feeding protocol for the control group. The field is further complicated when attempts are made to compare studies across different laboratories, which seemingly contradict each other. Here, we argue that some of the contradictory findings are most likely due to methodological differences. This review focuses on the four methodological differences identified in a recent comparative report from the National Institute on Aging and University of Wisconsin nonhuman primate studies, namely feeding regimen, diet composition, age of onset, and genetics. These factors, that may be influencing the effects of a calorie restriction intervention, are highlighted in the rodent model to draw parallels and elucidate findings reported in a higher species, nonhuman primates.

摘要

一个世纪以来,我们已经知道热量限制会影响许多物种的衰老。然而,直到最近才确凿地证实,这种影响并非完全取决于所提供的热量。相反,啮齿动物和非人类灵长类动物模型表明,衰老速度取决于其他变量,包括饮食中的宏量营养素组成、处于限制状态的时间、开始限制的年龄、性别和遗传背景,以及对照组的特定喂养方案。当试图比较不同实验室的研究结果时,这个领域变得更加复杂,因为这些结果似乎相互矛盾。在这里,我们认为一些相互矛盾的发现很可能是由于方法上的差异。这篇综述聚焦于美国国立衰老研究所和威斯康星大学非人类灵长类动物研究最近的一份比较报告中确定的四个方法上的差异,即喂养方案、饮食组成、开始限制的年龄和遗传学。这些可能影响热量限制干预效果的因素在啮齿动物模型中得到强调,以便进行类比并阐明在更高等物种——非人类灵长类动物中报道的研究结果。

相似文献

[1]
Caloric Restriction Study Design Limitations in Rodent and Nonhuman Primate Studies.

J Gerontol A Biol Sci Med Sci. 2017-12-12

[2]
Caloric Restriction and Healthy Life Span: Frail Phenotype of Nonhuman Primates in the Wisconsin National Primate Research Center Caloric Restriction Study.

J Gerontol A Biol Sci Med Sci. 2018-3-2

[3]
Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study.

Nature. 2012-9-13

[4]
[Aging and aging intervention by coloric restriction in nonhuman primate rhesus monkeys].

Sheng Li Ke Xue Jin Zhan. 2013-2

[5]
Nonhuman primate calorie restriction.

Antioxid Redox Signal. 2010-10-12

[6]
[Caloric restriction in primates: how efficient as an anti-aging approach?].

Med Sci (Paris). 2012-12

[7]
Nutrition and energetics in rodent longevity research.

Exp Gerontol. 2016-12-15

[8]
Role of caloric restriction in the prolongation of life.

Clin Geriatr Med. 1995-11

[9]
Nutrition, metabolism, and targeting aging in nonhuman primates.

Ageing Res Rev. 2017-10

[10]
Macronutrients and caloric intake in health and longevity.

J Endocrinol. 2015-7

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本文引用的文献

[1]
Caloric restriction improves health and survival of rhesus monkeys.

Nat Commun. 2017-1-17

[2]
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Cell Metab. 2016-6-14

[3]
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Cell Metab. 2016-6-14

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Calories or protein? The effect of dietary restriction on lifespan in rodents is explained by calories alone.

Exp Gerontol. 2016-12-15

[5]
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Cell. 2015-3-26

[6]
Time-restricted feeding is a preventative and therapeutic intervention against diverse nutritional challenges.

Cell Metab. 2014-12-2

[7]
The Influence of Dietary Fat Source on Life Span in Calorie Restricted Mice.

J Gerontol A Biol Sci Med Sci. 2014-10-13

[8]
Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction.

Longev Healthspan. 2012-9-3

[9]
The ratio of macronutrients, not caloric intake, dictates cardiometabolic health, aging, and longevity in ad libitum-fed mice.

Cell Metab. 2014-3-4

[10]
Prevalence of childhood and adult obesity in the United States, 2011-2012.

JAMA. 2014-2-26

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