Rebrin Igor, Forster Michael J, Sohal Rajindar S
Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, CA 90089, USA.
Brain Res. 2007 Jan 5;1127(1):10-8. doi: 10.1016/j.brainres.2006.10.040. Epub 2006 Nov 17.
The main purpose of the present study was to determine whether specific regions of the mouse brain exhibit different age-related changes in oxidative stress, as indicated by glutathione redox state and the level of protein-glutathionyl mixed disulfides. Comparison of 3- and 21-month-old mice indicated an age-related decrease in the ratio of reduced to oxidized glutathione (GSH/GSSG) as well as a pro-oxidizing shift in the calculated redox potential (ranging from 6 to 15 mV) in the cortex, hippocampus, striatum and cerebellum, whereas there was little change in the brainstem. This pro-oxidizing shift in redox state was due to a modest decrease in GSH content occurring in all the brain regions examined, and elevations in GSSG amount that were most pronounced in the striatum and cerebellum. The regional changes in glutathione redox state were paralleled by increases in the amounts of protein-mixed disulfides. A reduction of caloric intake by 40% for a short period (7 weeks), implemented in relatively old mice (17 months), increased the GSH/GSSG ratio and redox potential at 19 months in the same brain regions that exhibited age-related decreases. The effects of age and caloric restriction were qualitatively similar in C57BL/6 and DBA/2 mice. However, young DBA/2 mice, which do not show extension of life span in response to long-term caloric restriction, had lower GSH/GSSG ratios and higher protein-mixed disulfides than age-matched C57BL/6 mice. The current findings demonstrate that oxidative stress, as reflected by glutathione redox state, increases in the aging brain in regions linked to age-associated losses of function and neurodegenerative diseases.
本研究的主要目的是确定小鼠大脑的特定区域是否表现出与年龄相关的氧化应激变化,这可通过谷胱甘肽氧化还原状态和蛋白质-谷胱甘肽混合二硫化物水平来表明。对3月龄和21月龄小鼠的比较表明,在皮质、海马体、纹状体和小脑中,与年龄相关的变化表现为还原型谷胱甘肽与氧化型谷胱甘肽的比例(GSH/GSSG)下降,以及计算得出的氧化还原电位发生促氧化转变(范围为6至15 mV),而脑干中几乎没有变化。这种氧化还原状态的促氧化转变是由于在所检查的所有脑区中,谷胱甘肽含量适度下降,以及纹状体和小脑中最明显的氧化型谷胱甘肽量升高所致。谷胱甘肽氧化还原状态的区域变化与蛋白质混合二硫化物量的增加平行。在相对老龄的小鼠(17月龄)中短期(7周)减少40%的热量摄入,会使19月龄时相同脑区中呈现与年龄相关下降的谷胱甘肽氧化还原电位和GSH/GSSG比值增加。年龄和热量限制的影响在C57BL/6和DBA/2小鼠中在性质上相似。然而,年轻的DBA/2小鼠,对长期热量限制没有表现出寿命延长,其GSH/GSSG比值低于年龄匹配的C57BL/6小鼠,蛋白质混合二硫化物含量更高。目前的研究结果表明,以谷胱甘肽氧化还原状态反映的氧化应激在与年龄相关的功能丧失和神经退行性疾病相关的脑区中随着年龄增长而增加。