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在氧化应激条件下,叶酸和维生素E的膳食缺乏会增加磷酸化tau蛋白水平:载脂蛋白E4起增强作用,而S-腺苷甲硫氨酸起缓解作用。

Dietary deficiency in folate and vitamin E under conditions of oxidative stress increases phospho-tau levels: potentiation by ApoE4 and alleviation by S-adenosylmethionine.

作者信息

Chan Amy, Rogers Eugene, Shea Thomas B

机构信息

Center for Cellular Neurobiology and Neurodegeneration Research, Department of Biological Sciences, University of Massachusetts Lowell, Lowell, MA 01854, USA.

出版信息

J Alzheimers Dis. 2009;17(3):483-7. doi: 10.3233/JAD-2009-1076.

Abstract

Prior studies link dietary deficiency and genetic risk factors for Alzheimer's disease (AD). In the present report, mice expressing human apolipoprotein E4 (associated with increased risk of AD) and apolipoprotein E3 were subjected to a diet lacking folate and vitamin E, and containing iron as a pro-oxidant. Consistent with prior studies, E4 mice displayed more phospho-tau than E3 mice prior to dietary challenge. The deficient diet increased phospho-tau in E4 but not E3 mice, which was prevented by S-adenosyl methionine supplementation. Since neurofibrillary tangles are comprised of phospho-tau, investigation of the impact of dietary deficiency and S-adenosyl methionine supplementation on neurofibrillary tangle formation are warranted.

摘要

先前的研究将饮食缺乏和阿尔茨海默病(AD)的遗传风险因素联系起来。在本报告中,表达人类载脂蛋白E4(与AD风险增加相关)和载脂蛋白E3的小鼠被给予缺乏叶酸和维生素E且含有作为促氧化剂的铁的饮食。与先前的研究一致,在饮食挑战之前,E4小鼠比E3小鼠表现出更多的磷酸化tau蛋白。缺乏的饮食增加了E4小鼠而非E3小鼠的磷酸化tau蛋白,补充S-腺苷甲硫氨酸可预防这种情况。由于神经原纤维缠结由磷酸化tau蛋白组成,因此有必要研究饮食缺乏和补充S-腺苷甲硫氨酸对神经原纤维缠结形成的影响。

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