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衰老、静息代谢率与氧化损伤:来自路易斯安那州健康衰老研究的结果

Aging, resting metabolic rate, and oxidative damage: results from the Louisiana Healthy Aging Study.

作者信息

Frisard Madlyn I, Broussard Amanda, Davies Sean S, Roberts L Jackson, Rood Jennifer, de Jonge Lillian, Fang Xiaobing, Jazwinski S Michal, Deutsch Walter A, Ravussin Eric

机构信息

Pennington Biomedical Research Center, 6400 Perkins Rd., Baton Rouge, LA 70808, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2007 Jul;62(7):752-9. doi: 10.1093/gerona/62.7.752.

Abstract

BACKGROUND

The aging process occurs at variable rates both among and within species and may be related to the variability in oxygen consumption and free radical production impacting oxidative stress. The current study was designed to test whether nonagenarians have a relatively low metabolic rate and whether it is associated with low levels of oxidative stress relative to age.

METHODS

Resting metabolic rate (RMR) and markers of oxidative stress to lipids, proteins, and DNA were measured in three groups of individuals aged 20-34 (n=47), 60-74 (n=49), and>or=90 years (n=74).

RESULTS

RMR, adjusted for fat-free mass, fat mass, and sex, was lower in both older groups when compared to the young group (p<or=.0001). There were no significant differences in urinary isoprostanes, serum protein carbonyls, or DNA fragmentation between groups, and RMR was not related to any markers of oxidative stress.

CONCLUSIONS

This study confirms an age-related decline in RMR independent of changes in body composition but surprisingly did not show an accumulation of oxidative damage with increasing age. Our data challenge the theory that RMR is a significant determinant of oxidative stress and therefore contributes to the aging process.

摘要

背景

衰老过程在物种间和物种内以不同速率发生,可能与影响氧化应激的氧消耗和自由基产生的变异性有关。本研究旨在测试百岁老人是否具有相对较低的代谢率,以及这是否与相对于年龄的低水平氧化应激相关。

方法

测量了三组个体的静息代谢率(RMR)以及脂质、蛋白质和DNA氧化应激标志物,这三组个体年龄分别为20 - 34岁(n = 47)、60 - 74岁(n = 49)和≥90岁(n = 74)。

结果

在根据去脂体重、脂肪量和性别进行调整后,两个老年组的RMR均低于年轻组(p≤0.0001)。各组间尿异前列腺素、血清蛋白羰基或DNA片段化无显著差异,且RMR与任何氧化应激标志物均无关联。

结论

本研究证实了RMR随年龄下降,且独立于身体成分的变化,但令人惊讶的是,未显示氧化损伤随年龄增长而累积。我们的数据对RMR是氧化应激的重要决定因素并因此导致衰老过程这一理论提出了挑战。

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