López-Torres Mónica, Barja Gustavo
Departamento de Fisiología Animal II, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, Madrid, España.
Rev Esp Geriatr Gerontol. 2008 Jul-Aug;43(4):252-60. doi: 10.1016/s0211-139x(08)71190-9.
Studies on the relationship between oxidative stress and ageing in different vertebrate species and in calorie-restricted animals are reviewed. Endogenous antioxidants inversely correlate with maximum longevity in animal species and experiments modifying levels of these antioxidants can increase survival and mean life span but not maximum life span (MLSP). The available evidence shows that long-living vertebrates consistently have low rates of mitochondrial free radical generation, as well as a low grade of fatty acid unsaturation on cellular membranes, which are two crucial factors determining their ageing rate. Oxidative damage to mitochondrial DNA is also lower in long-living vertebrates than in short-living vertebrates. Calorie restriction, the best described experimental strategy that consistently increases mean and maximum life span, also decreases mitochondrial reactive oxygen species (ROS) generation and oxidative damage to mitochondrial DNA. Recent data indicate that the decrease in mitochondrial ROS generation is due to protein restriction rather than to calorie restriction, and more specifically to dietary methionine restriction. Greater longevity would be partly achieved by a low rate of endogenous oxidative damage generation, but also by a macromolecular composition highly resistant to oxidative modification, as is the case for lipids and proteins.
本文综述了关于不同脊椎动物物种以及限食动物中氧化应激与衰老之间关系的研究。内源性抗氧化剂与动物物种的最长寿命呈负相关,改变这些抗氧化剂水平的实验可以提高存活率和平均寿命,但不能延长最长寿命(MLSP)。现有证据表明,长寿脊椎动物的线粒体自由基产生率始终较低,细胞膜上的脂肪酸不饱和度也较低,这是决定其衰老速度的两个关键因素。长寿脊椎动物中线粒体DNA的氧化损伤也低于短寿脊椎动物。限食是一种被充分描述的实验策略,它能持续增加平均寿命和最长寿命,同时也能减少线粒体活性氧(ROS)的产生以及线粒体DNA的氧化损伤。最近的数据表明,线粒体ROS产生的减少是由于蛋白质限制而非热量限制,更具体地说是由于饮食中的蛋氨酸限制。更长的寿命部分是通过低水平的内源性氧化损伤产生实现的,同时也得益于脂质和蛋白质等对氧化修饰具有高度抗性的大分子组成。