Department of Pharmacology, School of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Probiotics Australia, Ormeau, QLD, Australia.
J Alzheimers Dis. 2020;73(3):849-865. doi: 10.3233/JAD-190872.
Alzheimer's disease (AD) is a neurodegenerative process characterized by loss of neurons in the hippocampus and cerebral cortex, leading to progressive cognitive decline. Pathologically, the hallmark of AD is accumulation of "senile" plaques composed of amyloid-β (Aβ) protein surrounding neurons in affected regions. Despite extensive research into AD pathogenesis and therapeutic targets, there remains no breakthroughs in its management. In recent years, there has been a spark of interest in the connection between the brain and gastrointestinal tract, referred to as the brain-gut axis, and its potential implications for both metabolic and neurologic disease. Moreover, the gastrointestinal flora, referred to as the microbiome, appears to exert significant influence over the brain-gut axis. With the need for expanded horizons in understanding and treating AD, many have turned to the brain-gut-microbiome axis for answers. Here we provide a review of the brain-gut-microbiome axis and discuss the evidence supporting alterations of the axis in the pathogenesis of AD. Specifically, we highlight the role for the microbiome in disruption of Aβ metabolism/clearance, increased permeability of the blood-brain barrier and modulation of the neuroinflammatory response, and inhibition of hippocampal neurogenesis. The majority of the above described findings are the result of excellent, albeit basic and pre-clinical studies. Therefore, we conclude with a brief description of documented clinical support for brain-gut-microbiome axis alteration in AD, including potential microbiome-based therapeutics for AD. Collectively, these findings suggest that the brain-gut-microbiome axis may be a "lost link" in understanding and treating AD and call for future work.
阿尔茨海默病(AD)是一种神经退行性疾病,其特征是海马体和大脑皮层神经元的丧失,导致进行性认知能力下降。从病理学角度来看,AD 的标志是受影响区域神经元周围的淀粉样β(Aβ)蛋白积累形成的“老年”斑块。尽管对 AD 的发病机制和治疗靶点进行了广泛的研究,但在其管理方面仍未取得突破。近年来,人们对大脑和胃肠道之间的联系(称为脑-肠轴)及其对代谢和神经疾病的潜在影响产生了兴趣。此外,胃肠道菌群(称为微生物组)似乎对脑-肠轴有重大影响。为了扩大对 AD 的理解和治疗范围,许多人开始关注脑-肠-微生物组轴以寻求答案。在这里,我们回顾了脑-肠-微生物组轴,并讨论了支持该轴在 AD 发病机制中发生改变的证据。具体而言,我们强调了微生物组在破坏 Aβ代谢/清除、增加血脑屏障通透性以及调节神经炎症反应和抑制海马神经发生方面的作用。上述大部分发现都是基于优秀的基础和临床前研究的结果。因此,我们简要描述了 AD 中脑-肠-微生物组轴改变的临床证据,包括潜在的基于微生物组的 AD 治疗方法。综上所述,这些发现表明,脑-肠-微生物组轴可能是理解和治疗 AD 的“缺失环节”,并呼吁开展进一步的研究。