Wiȩckowska-Gacek Angelika, Mietelska-Porowska Anna, Chutorański Dominik, Wydrych Małgorzata, Długosz Jan, Wojda Urszula
Laboratory of Preclinical Testing of Higher Standard, Neurobiology Center, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Front Aging Neurosci. 2021 Apr 1;13:654509. doi: 10.3389/fnagi.2021.654509. eCollection 2021.
Alzheimer's disease (AD) is an aging-dependent, irreversible neurodegenerative disorder and the most common cause of dementia. The prevailing AD hypothesis points to the central role of altered cleavage of amyloid precursor protein (APP) and formation of toxic amyloid-β (Aβ) deposits in the brain. The lack of efficient AD treatments stems from incomplete knowledge on AD causes and environmental risk factors. The role of lifestyle factors, including diet, in neurological diseases is now beginning to attract considerable attention. One of them is western diet (WD), which can lead to many serious diseases that develop with age. The aim of the study was to investigate whether WD-derived systemic disturbances may accelerate the brain neuroinflammation and amyloidogenesis at the early stages of AD development. To verify this hypothesis, transgenic mice expressing human APP with AD-causing mutations (APPswe) were fed with WD from the 3rd month of age. These mice were compared to APPswe mice, in which short-term high-grade inflammation was induced by injection of lipopolysaccharide (LPS) and to untreated APPswe mice. All experimental subgroups of animals were subsequently analyzed at 4-, 8-, and 12-months of age. APPswe mice at 4- and 8-months-old represent earlier pre-plaque stages of AD, while 12-month-old animals represent later stages of AD, with visible amyloid pathology. Already short time of WD feeding induced in 4-month-old animals such brain neuroinflammation events as enhanced astrogliosis, to a level comparable to that induced by the administration of pro-inflammatory LPS, and microglia activation in 8-month-old mice. Also, WD feeding accelerated increased Aβ production, observed already in 8-month-old animals. These brain changes corresponded to diet-induced metabolic disorders, including increased cholesterol level in 4-months of age, and advanced hypercholesterolemia and fatty liver disease in 8-month-old mice. These results indicate that the westernized pattern of nourishment is an important modifiable risk factor of AD development, and that a healthy, balanced, diet may be one of the most efficient AD prevention methods.
阿尔茨海默病(AD)是一种与衰老相关的、不可逆的神经退行性疾病,也是痴呆最常见的病因。目前流行的AD假说指出,淀粉样前体蛋白(APP)异常切割以及脑内有毒性的淀粉样β蛋白(Aβ)沉积起着核心作用。缺乏有效的AD治疗方法源于对AD病因和环境风险因素的认识不足。包括饮食在内的生活方式因素在神经疾病中的作用现在开始受到相当多的关注。其中之一是西式饮食(WD),它会导致许多随年龄增长而出现的严重疾病。本研究的目的是调查WD引起的全身紊乱是否会在AD发展的早期阶段加速脑内神经炎症和淀粉样蛋白生成。为了验证这一假说,从3月龄开始给表达具有AD致病突变的人APP(APPswe)的转基因小鼠喂食WD。将这些小鼠与通过注射脂多糖(LPS)诱导短期高度炎症的APPswe小鼠以及未处理的APPswe小鼠进行比较。随后在4、8和12月龄时对所有动物实验亚组进行分析。4月龄和8月龄的APPswe小鼠代表AD的早期斑块前阶段,而12月龄的动物代表AD的晚期阶段,有明显的淀粉样病理改变。仅短期喂食WD就在4月龄动物中引发了脑内神经炎症事件,如星形胶质细胞增生增强,达到了与给予促炎LPS诱导的水平相当,并且在8月龄小鼠中引发了小胶质细胞激活。此外,喂食WD加速了Aβ生成增加,在8月龄动物中就已观察到。这些脑内变化与饮食诱导的代谢紊乱相对应,包括4月龄时胆固醇水平升高,以及8月龄小鼠出现晚期高胆固醇血症和脂肪肝疾病。这些结果表明,西式营养模式是AD发展的一个重要的可改变风险因素,健康、均衡的饮食可能是最有效的AD预防方法之一。