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[使用SMP30/GNL基因敲除小鼠的抗衰老研究]

[Anti-aging research using SMP30/GNL knockout mice].

作者信息

Ishigami Akihito

机构信息

Department of Biochemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Chiba, Japan.

出版信息

Yakugaku Zasshi. 2010 Jan;130(1):25-8. doi: 10.1248/yakushi.130.25.

Abstract

Senescence Marker Protein-30 (SMP30) was originally identified as a novel protein in the rat liver, the expression of which decreases with aging. Recently, we identified SMP30 as the lactone-hydrolyzing enzyme gluconolactonases (GNL) of animal species. GNL was a key enzyme which involved in vitamin C biosynthesis, and the essential role of SMP30 in this synthetic process was verified by a nutritional study. SMP30 knockout mice developed symptoms of scurvy when fed a vitamin C-deficient diet, verifying the pivotal role of SMP30 in vitamin C biosynthesis. Moreover, SMP30 knockout mice were shorter in life span than the wild type when fed autoclaved mouse chow contained approximately 55 mg/kg of vitamin C, which we now know contains too little vitamin C to maintain normal levels of vitamin C in tissues. These results demonstrate that vitamin C deficiency shortens longevity, that is, vitamin C deficiency accelerates aging.

摘要

衰老标记蛋白-30(SMP30)最初是在大鼠肝脏中被鉴定为一种新蛋白,其表达随衰老而降低。最近,我们将SMP30鉴定为动物物种的内酯水解酶葡糖酸内酯酶(GNL)。GNL是参与维生素C生物合成的关键酶,一项营养研究证实了SMP30在这一合成过程中的重要作用。当给SMP30基因敲除小鼠喂食缺乏维生素C的饮食时,它们出现了坏血病症状,证实了SMP30在维生素C生物合成中的关键作用。此外,当给SMP30基因敲除小鼠喂食含有约55毫克/千克维生素C的高压灭菌小鼠饲料时,其寿命比野生型短,我们现在知道这种饲料所含的维生素C太少,无法维持组织中维生素C的正常水平。这些结果表明,维生素C缺乏会缩短寿命,即维生素C缺乏会加速衰老。

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