Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, TX 78245, USA.
Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, TX 78245, USA; Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, TX 78245.
Free Radic Biol Med. 2014 Jan;66:88-99. doi: 10.1016/j.freeradbiomed.2013.05.037. Epub 2013 Jun 4.
Oxidative stress is observed during aging and in numerous age-related diseases. Dietary restriction (DR) is a regimen that protects against disease and extends life span in multiple species. However, it is unknown how DR mediates its protective effects. One prominent and consistent effect of DR in a number of systems is the ability to reduce oxidative stress and damage. The purpose of this review is to comprehensively examine the hypothesis that dietary restriction reduces oxidative stress in rodents by decreasing reactive oxygen species (ROS) production and increasing antioxidant enzyme activity, leading to an overall reduction of oxidative damage to macromolecules. The literature reveals that the effects of DR on oxidative stress are complex and likely influenced by a variety of factors, including sex, species, tissue examined, types of ROS and antioxidant enzymes examined, and duration of DR. Here we present a comprehensive review of the existing literature on the effect of DR on mitochondrial ROS generation, antioxidant enzymes, and oxidative damage. In a majority of studies, dietary restriction had little effect on mitochondrial ROS production or antioxidant activity. On the other hand, DR decreased oxidative damage in the majority of cases. Although the effects of DR on endogenous antioxidants are mixed, we find that glutathione levels are the most likely antioxidant to be increased by dietary restriction, which supports the emerging redox-stress hypothesis of aging.
氧化应激在衰老和许多与年龄相关的疾病中都存在。饮食限制(DR)是一种可以预防疾病并延长多种物种寿命的方案。然而,尚不清楚 DR 如何介导其保护作用。DR 在许多系统中一个突出且一致的作用是降低氧化应激和损伤的能力。本综述的目的是全面研究这样一个假设,即饮食限制通过减少活性氧(ROS)的产生和增加抗氧化酶的活性来降低啮齿动物的氧化应激,从而导致大分子氧化损伤的总体减少。文献表明,DR 对氧化应激的影响是复杂的,可能受到多种因素的影响,包括性别、物种、所检查的组织、所检查的 ROS 和抗氧化酶的类型以及 DR 的持续时间。在这里,我们对关于 DR 对线粒体 ROS 生成、抗氧化酶和氧化损伤影响的现有文献进行了全面回顾。在大多数研究中,饮食限制对线粒体 ROS 产生或抗氧化活性几乎没有影响。另一方面,DR 在大多数情况下降低了氧化损伤。尽管 DR 对内源性抗氧化剂的影响是混合的,但我们发现,谷胱甘肽水平最有可能被饮食限制所增加,这支持了新兴的衰老氧化应激假说。