Suppr超能文献

肠道微生物组改变与阿尔茨海默病炎症驱动发病机制:一项关键性综述

The Gut Microbiome Alterations and Inflammation-Driven Pathogenesis of Alzheimer's Disease-a Critical Review.

机构信息

Laboratory of Virology, Department of Immunology of Infectious Diseases, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.

Laboratory of Parasitology, General Karol Kaczkowski Military Institute of Hygiene and Epidemiology, Warsaw, Poland.

出版信息

Mol Neurobiol. 2019 Mar;56(3):1841-1851. doi: 10.1007/s12035-018-1188-4. Epub 2018 Jun 23.

Abstract

One of the most important scientific discoveries of recent years was the disclosure that the intestinal microflora takes part in bidirectional communication between the gut and the brain. Scientists suggest that human gut microflora may even act as the "second brain" and be responsible for neurodegenerative disorders like Alzheimer's disease (AD). Although human-associated microbial communities are generally stable, they can be altered by common human actions and experiences. Enteric bacteria, commensal, and pathogenic microorganisms, may have a major impact on immune system, brain development, and behavior, as they are able to produce several neurotransmitters and neuromodulators like serotonin, kynurenine, catecholamine, etc., as well as amyloids. However, brain destructive mechanisms, that can lead to dementia and AD, start with the intestinal microbiome dysbiosis, development of local and systemic inflammation, and dysregulation of the gut-brain axis. Increased permeability of the gut epithelial barrier results in invasion of different bacteria, viruses, and their neuroactive products that support neuroinflammatory reactions in the brain. It seems that, inflammatory-infectious hypothesis of AD, with the great role of the gut microbiome, starts to gently push into the shadow the amyloid cascade hypothesis that has dominated for decades. It is strongly postulated that AD may begin in the gut, and is closely related to the imbalance of gut microbiota. This is promising area for therapeutic intervention. Modulation of gut microbiota through personalized diet or beneficial microbiota intervention, alter microbial partners and their products including amyloid protein, will probably become a new treatment for AD.

摘要

近年来最重要的科学发现之一是揭示了肠道微生物群参与肠道和大脑之间的双向通讯。科学家们认为,人类肠道微生物群甚至可能充当“第二大脑”,并负责阿尔茨海默病(AD)等神经退行性疾病。尽管与人类相关的微生物群落通常是稳定的,但它们可以通过常见的人类行为和经验而改变。肠细菌、共生菌和病原微生物可能会对免疫系统、大脑发育和行为产生重大影响,因为它们能够产生几种神经递质和神经调质,如血清素、犬尿氨酸、儿茶酚胺等,以及淀粉样蛋白。然而,导致痴呆和 AD 的大脑破坏性机制始于肠道微生物组失调、局部和全身炎症的发展以及肠道-大脑轴的失调。肠道上皮屏障的通透性增加导致不同细菌、病毒及其神经活性产物的入侵,从而支持大脑中的神经炎症反应。似乎,AD 的炎症-感染假说,加上肠道微生物群的重要作用,开始温和地将主导了几十年的淀粉样蛋白级联假说推向阴影。强烈假设 AD 可能始于肠道,并与肠道微生物群失衡密切相关。这是治疗干预的有前途的领域。通过个性化饮食或有益微生物群干预来调节肠道微生物群,改变微生物伙伴及其产物,包括淀粉样蛋白,可能成为 AD 的新治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d1/6394610/3a0709e66b87/12035_2018_1188_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验