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可食用叶酸对早发型三转基因阿尔茨海默病模型小鼠心肌细胞凋亡和存活的预防作用。

The preventive effects of edible folic acid on cardiomyocyte apoptosis and survival in early onset triple-transgenic Alzheimer's disease model mice.

作者信息

Lin Kuan-Ho, Chiu Chih-Hao, Kuo Wei-Wen, Ju Da-Tong, Shen Chia-Yao, Chen Ray-Jade, Lin Chien-Chung, Viswanadha Vijaya Padma, Liu Jian-Sheng, Huang Rwei-Fen S, Huang Chih-Yang

机构信息

College of Medicine, China Medical University, Taichung, Taiwan.

Department of Emergency Medicine, China Medical University Hospital, Taichung, Taiwan.

出版信息

Environ Toxicol. 2018 Jan;33(1):83-92. doi: 10.1002/tox.22498. Epub 2017 Oct 25.

DOI:10.1002/tox.22498
PMID:29068127
Abstract

In recent years, neuropathological and epidemiological studies have indicated an association between Alzheimer's disease (AD) and several cardiovascular risk factors. In this study, the cardio-protective effects of folic acid (FA) in early stage AD was elucidated using a triple-transgenic (3xTg) Alzheimer's mouse model. Eleven-month-old C57BL/6 mice and 3xTg mice were assigned to five groups. During the four-month treatment period, the low-FA treatment group received FA through their diet, and the high-FA treatment groups received 3 mg/dl folate in drinking water and were also gastric-fed 1.2 mg/kg folate every day. In the C57B1/6J mice, treatment with high doses of FA (HFA) did not show any considerable effect compared to the control group or the low-dose dietary FA treatment group. However, Alzheimer's mice treated with HFA showed enhanced cardio-protection. Western blot analysis revealed that FA treatment restored SIRT1 expression, which was suppressed in 3xTg mice, through enhanced AMPK expression. FA significantly enhanced the IGF1 receptor survival mechanism in the hearts of the 3xTg mice and suppressed the expression-intrinsic and extrinsic apoptosis-associated proteins. The results suggest that FA intake may significantly alleviate cellular pathological events in the heart associated with AD.

摘要

近年来,神经病理学和流行病学研究表明,阿尔茨海默病(AD)与多种心血管危险因素之间存在关联。在本研究中,使用三转基因(3xTg)阿尔茨海默病小鼠模型阐明了叶酸(FA)在早期AD中的心脏保护作用。将11个月大的C57BL/6小鼠和3xTg小鼠分为五组。在为期四个月的治疗期内,低叶酸治疗组通过饮食摄入叶酸,高叶酸治疗组在饮用水中摄入3mg/dl叶酸,并且每天还通过胃管给予1.2mg/kg叶酸。在C57B1/6J小鼠中,与对照组或低剂量饮食叶酸治疗组相比,高剂量叶酸(HFA)治疗未显示出任何显著效果。然而,用HFA治疗的阿尔茨海默病小鼠表现出增强的心脏保护作用。蛋白质印迹分析显示,叶酸治疗通过增强AMPK表达恢复了在3xTg小鼠中被抑制的SIRT1表达。叶酸显著增强了3xTg小鼠心脏中的IGF1受体存活机制,并抑制了内在和外在凋亡相关蛋白的表达。结果表明,摄入叶酸可能显著减轻与AD相关的心脏细胞病理事件。

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