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首页> 外文期刊>Brain research >Effects of age and caloric intake on glutathione redox state in different brain regions of C57BL/6 and DBA/2 mice.
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Effects of age and caloric intake on glutathione redox state in different brain regions of C57BL/6 and DBA/2 mice.

机译:年龄和热量摄入对C57BL / 6和DBA / 2小鼠不同大脑区域的谷胱甘肽氧化还原状态的影响。

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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.
机译: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,如谷胱甘肽氧化还原状态和蛋白质-谷胱甘肽混合二硫化物的水平所表明的。比较3个月和21个月大的小鼠,发现还原型与氧化型谷胱甘肽(GSH / GSSG)的比例与年龄相关,并且计算的氧化还原电势发生了前氧化变化(范围从6到15 mV) )在皮层,海马,纹状体和小脑中,而脑干几乎没有变化。氧化还原状态的这种促氧化转变是由于在所有检查的大脑区域中发生的GSH含量适度降低,以及纹状体和小脑中最明显的GSSG含量升高。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数量的增加平行。在相对较大的小鼠(17个月)中,在短时间内(7周)减少了40%的热量摄入,在与年龄相关的降低的同一大脑区域中,GSH / GSSG比和氧化还原电位在19个月时增加了。 C57BL / 6和DBA / 2小鼠的年龄和热量限制的影响在质量上相似。但是,与长期匹配的C57BL / 6小鼠相比,年轻的DBA / 2小鼠并未显示出响应长期热量限制的寿命延长,其GSH / GSSG比率较低,蛋白质混合的二硫键含量更高。目前的发现表明,谷胱甘肽氧化还原状态所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有关的区域中的衰老大脑中增加。

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