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帕金森病中的脑-肠-微生物群轴

Brain-gut-microbiota axis in Parkinson's disease.

作者信息

Mulak Agata, Bonaz Bruno

机构信息

Agata Mulak, Department of Gastroenterology and Hepatology, Wroclaw Medical University, 50-556 Wroclaw, Poland.

出版信息

World J Gastroenterol. 2015 Oct 7;21(37):10609-20. doi: 10.3748/wjg.v21.i37.10609.

Abstract

Parkinson's disease (PD) is characterized by alpha-synucleinopathy that affects all levels of the brain-gut axis including the central, autonomic, and enteric nervous systems. Recently, it has been recognized that the brain-gut axis interactions are significantly modulated by the gut microbiota via immunological, neuroendocrine, and direct neural mechanisms. Dysregulation of the brain-gut-microbiota axis in PD may be associated with gastrointestinal manifestations frequently preceding motor symptoms, as well as with the pathogenesis of PD itself, supporting the hypothesis that the pathological process is spread from the gut to the brain. Excessive stimulation of the innate immune system resulting from gut dysbiosis and/or small intestinal bacterial overgrowth and increased intestinal permeability may induce systemic inflammation, while activation of enteric neurons and enteric glial cells may contribute to the initiation of alpha-synuclein misfolding. Additionally, the adaptive immune system may be disturbed by bacterial proteins cross-reacting with human antigens. A better understanding of the brain-gut-microbiota axis interactions should bring a new insight in the pathophysiology of PD and permit an earlier diagnosis with a focus on peripheral biomarkers within the enteric nervous system. Novel therapeutic options aimed at modifying the gut microbiota composition and enhancing the intestinal epithelial barrier integrity in PD patients could influence the initial step of the following cascade of neurodegeneration in PD.

摘要

帕金森病(PD)的特征是α-突触核蛋白病,它会影响脑-肠轴的各个层面,包括中枢神经系统、自主神经系统和肠神经系统。最近,人们认识到肠道微生物群通过免疫、神经内分泌和直接神经机制对脑-肠轴的相互作用有显著调节作用。PD中脑-肠-微生物群轴的失调可能与运动症状之前频繁出现的胃肠道表现以及PD本身的发病机制有关,这支持了病理过程从肠道传播到大脑的假说。肠道生态失调和/或小肠细菌过度生长以及肠道通透性增加导致的先天免疫系统过度刺激可能会引发全身炎症,而肠神经元和肠胶质细胞的激活可能会促使α-突触核蛋白错误折叠的起始。此外,适应性免疫系统可能会受到与人类抗原有交叉反应的细菌蛋白的干扰。更好地理解脑-肠-微生物群轴的相互作用应该会为PD的病理生理学带来新的见解,并允许以肠神经系统中的外周生物标志物为重点进行早期诊断。旨在改变PD患者肠道微生物群组成并增强肠道上皮屏障完整性的新型治疗选择可能会影响PD中随后一系列神经退行性变的初始步骤。

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