Pamplona Reinald, Barja Gustavo
Department of Basic Medical Sciences, University of Lleida, Lleida 25008, Spain.
Biochim Biophys Acta. 2006 May-Jun;1757(5-6):496-508. doi: 10.1016/j.bbabio.2006.01.009. Epub 2006 Feb 24.
Caloric restriction (CR) decreases aging rate and mitochondrial ROS (MitROS) production and oxidative stress in rat postmitotic tissues. Low levels of these parameters are also typical traits of long-lived mammals and birds. However, it is not known what dietary components are responsible for these changes during CR. It was recently observed that 40% protein restriction without strong CR also decreases MitROS generation and oxidative stress. This is interesting because protein restriction also increases maximum longevity (although to a lower extent than CR) and is a much more practicable intervention for humans than CR. Moreover, it was recently found that 80% methionine restriction substituting it for l-glutamate in the diet also decreases MitROS generation in rat liver. Thus, methionine restriction seems to be responsible for the decrease in ROS production observed in caloric restriction. This is interesting because it is known that exactly that procedure of methionine restriction also increases maximum longevity. Moreover, recent data show that methionine levels in tissue proteins negatively correlate with maximum longevity in mammals and birds. All these suggest that lowering of methionine levels is involved in the control of mitochondrial oxidative stress and vertebrate longevity by at least two different mechanisms: decreasing the sensitivity of proteins to oxidative damage, and lowering of the rate of ROS generation at mitochondria.
热量限制(CR)可降低大鼠有丝分裂后组织的衰老速率、线粒体活性氧(MitROS)生成以及氧化应激。这些参数的低水平也是长寿哺乳动物和鸟类的典型特征。然而,目前尚不清楚在热量限制期间是哪些饮食成分导致了这些变化。最近观察到,在没有严格热量限制的情况下,40%的蛋白质限制也能减少MitROS的产生和氧化应激。这很有趣,因为蛋白质限制也能延长最大寿命(尽管程度低于热量限制),而且对人类来说,蛋白质限制比热量限制更具可行性。此外,最近发现,在饮食中用L-谷氨酸替代80%的蛋氨酸也能减少大鼠肝脏中的MitROS生成。因此,蛋氨酸限制似乎是热量限制中观察到的活性氧产生减少的原因。这很有趣,因为众所周知,正是这种蛋氨酸限制程序也能延长最大寿命。此外,最近的数据表明,组织蛋白中的蛋氨酸水平与哺乳动物和鸟类的最大寿命呈负相关。所有这些都表明,蛋氨酸水平的降低至少通过两种不同机制参与了线粒体氧化应激和脊椎动物寿命的调控:降低蛋白质对氧化损伤的敏感性,以及降低线粒体活性氧的生成速率。