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重新审视衰老的自由基理论:衰老的细胞信号中断理论。

The free radical theory of aging revisited: the cell signaling disruption theory of aging.

机构信息

Department of Physiology, University of Valencia and Fundacion Investigacion Hospital Clinico Universitario/INCLIVA, Valencia 46010, Spain.

出版信息

Antioxid Redox Signal. 2013 Sep 10;19(8):779-87. doi: 10.1089/ars.2012.5111.

Abstract

SIGNIFICANCE

The free radical theory of aging has provided a theoretical framework for an enormous amount of work leading to significant advances in our understanding of aging. Up to the turn of the century, the theory received abundant support from observations coming from fields as far apart as comparative physiology or molecular biology.

RECENT ADVANCES

Work from many laboratories supports the theory, for instance showing that overexpression of antioxidant enzymes results in increases in life-span. But other labs have shown that in some cases, there is an increased oxidative stress and increased longevity. The discovery that free radicals can not only cause molecular damage to cells, but also serve as signals; led to the proposal that they act as modulators of physiological processes. For instance, reactive oxygen species (ROS) stimulate physiological adaptations to physical exercise.

CRITICAL ISSUES

A critical blow to the free radical theory of aging came from epidemiological studies showing that antioxidant supplementation did not lower the incidence of many age-associated diseases but, in some cases, increased the risk of death. Moreover, recent molecular evidence has shown that increasing generation of ROS, in some cases, increases longevity.

FUTURE DIRECTIONS

Gerontologists interested in free radical biology are at a crossroads and clearly new insights are required to clarify the role of ROS in the process of aging. The hurdles are, no doubt, very high, but the intellectual and practical promise of these studies is of such magnitude that we feel that all efforts will be generously rewarding.

摘要

意义

衰老的自由基理论为大量工作提供了理论框架,这些工作极大地促进了我们对衰老的理解。在本世纪之交之前,该理论得到了来自生理学或分子生物学等领域的观察结果的充分支持。

最新进展

许多实验室的工作支持这一理论,例如,过表达抗氧化酶会导致寿命延长。但其他实验室表明,在某些情况下,氧化应激增加,寿命延长。自由基不仅可以对细胞造成分子损伤,还可以作为信号的发现,导致自由基作为生理过程调节剂的提议。例如,活性氧(ROS)刺激对体育锻炼的生理适应。

关键问题

来自流行病学研究的一个对衰老自由基理论的重大打击表明,抗氧化补充剂并没有降低许多与年龄相关的疾病的发病率,但在某些情况下,增加了死亡的风险。此外,最近的分子证据表明,在某些情况下,ROS 的产生增加会延长寿命。

未来方向

对自由基生物学感兴趣的老年病学家正处于十字路口,显然需要新的见解来阐明 ROS 在衰老过程中的作用。障碍无疑是非常高的,但这些研究的智力和实际承诺是如此之大,以至于我们觉得所有的努力都将得到丰厚的回报。

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