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叶酸给药可抑制APP/PS1转基因小鼠中淀粉样β肽的积累。

Folic acid administration inhibits amyloid β-peptide accumulation in APP/PS1 transgenic mice.

作者信息

Li Wen, Liu Huan, Yu Min, Zhang Xumei, Zhang Meilin, Wilson John X, Huang Guowei

机构信息

Department of Nutrition and Food Science, School of Public Health, Tianjin Medical University, Tianjin, China.

Department of Exercise and Nutrition Sciences, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.

出版信息

J Nutr Biochem. 2015 Aug;26(8):883-91. doi: 10.1016/j.jnutbio.2015.03.009. Epub 2015 Apr 28.

Abstract

Alzheimer's disease (AD) is associated with malnutrition, altered one-carbon metabolism and increased hippocampal amyloid-β peptide (Aβ) accumulation. Aberrant DNA methylation may be an epigenetic mechanism that underlies AD pathogenesis. We hypothesized that folic acid acts through an epigenetic gene silencing mechanism to lower Aβ levels in the APP/PS1 transgenic mouse model of AD. APP/PS1 mice were fed either folate-deficient or control diets and gavaged daily with 120 μg/kg folic acid, 13.3mg/kg S-adenosylmethionine (SAM) or both. Examination of the mice after 60 days of treatment showed that serum folate concentration increased with intake of folic acid but not SAM. Folate deficiency lowered endogenous SAM concentration, whereas neither intervention altered S-adenosylhomocysteine concentration. DNA methyltransferase (DNMT) activity increased with intake of folic acid raised DNMT activity in folate-deficient mice. DNA methylation rate was stimulated by folic acid in the amyloid precursor protein (APP) promoter and in the presenilin 1 (PS1) promoter. Folate deficiency elevated hippocampal APP, PS1 and Aβ protein levels, and these rises were prevented by folic acid. In conclusion, these findings are consistent with a mechanism in which folic acid increases methylation potential and DNMT activity, modifies DNA methylation and ultimately decreases APP, PS1 and Aβ protein levels.

摘要

阿尔茨海默病(AD)与营养不良、一碳代谢改变及海马区淀粉样β肽(Aβ)蓄积增加有关。异常的DNA甲基化可能是AD发病机制的一种表观遗传机制。我们假设叶酸通过一种表观遗传基因沉默机制来降低AD的APP/PS1转基因小鼠模型中的Aβ水平。给APP/PS1小鼠喂食叶酸缺乏或对照饮食,并每天灌胃120μg/kg叶酸、13.3mg/kg S-腺苷甲硫氨酸(SAM)或两者。治疗60天后对小鼠进行检查,结果显示血清叶酸浓度随叶酸摄入量增加而升高,但不随SAM摄入量增加而升高。叶酸缺乏会降低内源性SAM浓度,而两种干预措施均未改变S-腺苷同型半胱氨酸浓度。DNA甲基转移酶(DNMT)活性随叶酸摄入量增加而升高,在叶酸缺乏的小鼠中提高了DNMT活性。叶酸刺激淀粉样前体蛋白(APP)启动子和早老素1(PS1)启动子中的DNA甲基化率。叶酸缺乏会提高海马区APP、PS1和Aβ蛋白水平,而叶酸可防止这些升高。总之,这些发现与叶酸增加甲基化潜能和DNMT活性、改变DNA甲基化并最终降低APP、PS1和Aβ蛋白水平的机制一致。

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