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帕金森病中的肠道微生物组:罪魁祸首还是旁观者?

The gut microbiome in Parkinson's disease: A culprit or a bystander?

机构信息

Department of Internal Medicine, Division of Digestive Disease and Nutrition, Rush University Medical Center, Chicago, IL, United States.

Parkinson Institute, ASST Gaetano Pini-CTO, Milan, Italy.

出版信息

Prog Brain Res. 2020;252:357-450. doi: 10.1016/bs.pbr.2020.01.004. Epub 2020 Mar 5.

Abstract

In recent years, large-scale metagenomics projects such as the Human Microbiome Project placed the gut microbiota under the spotlight of research on its role in health and in the pathogenesis several diseases, as it can be a target for novel therapeutical approaches. The emerging concept of a microbiota modulation of the gut-brain axis in the pathogenesis of neurodegenerative disorders has been explored in several studies in animal models, as well as in human subjects. Particularly, research on changes in the composition of gut microbiota as a potential trigger for alpha-synuclein (α-syn) pathology in Parkinson's disease (PD) has gained increasing interest. In the present review, we first provide the basis to the understanding of the role of gut microbiota in healthy subjects and the molecular basis of the gut-brain interaction, focusing on metabolic and neuroinflammatory factors that could trigger the alpha-synuclein conformational changes and aggregation. Then, we critically explored preclinical and clinical studies reporting on the changes in gut microbiota in PD, as compared to healthy subjects. Furthermore, we examined the relationship between the gut microbiota and PD clinical features, discussing data consistently reported across studies, as well as the potential sources of inconsistencies. As a further step toward understanding the effects of gut microbiota on PD, we discussed the relationship between dysbiosis and response to dopamine replacement therapy, focusing on Levodopa metabolism. We conclude that further studies are needed to determine whether the gut microbiota changes observed so far in PD patients is the cause or, instead, it is merely a consequence of lifestyle changes associated with the disease. Regardless, studies so far strongly suggest that changes in microbiota appears to be impactful in pathogenesis of neuroinflammation. Thus, dysbiotic microbiota in PD could influence the disease course and response to medication, especially Levodopa. Future research will assess the impact of microbiota-directed therapeutic intervention in PD patients.

摘要

近年来,人类微生物组计划等大规模宏基因组学项目将肠道微生物组置于研究其在健康和几种疾病发病机制中的作用的焦点之下,因为它可能成为新的治疗方法的靶点。在动物模型以及人类研究中,已经探索了肠道微生物群调节在神经退行性疾病发病机制中的肠-脑轴的新兴概念。特别是,研究肠道微生物群组成的变化作为帕金森病(PD)中α-突触核蛋白(α-syn)病理学的潜在触发因素的研究越来越受到关注。在本综述中,我们首先提供了理解肠道微生物群在健康受试者中的作用以及肠-脑相互作用的分子基础的基础,重点关注可能引发α-突触核蛋白构象变化和聚集的代谢和神经炎症因子。然后,我们批判性地探讨了报告 PD 中肠道微生物群变化的临床前和临床研究,与健康受试者相比。此外,我们检查了肠道微生物群与 PD 临床特征之间的关系,讨论了跨研究一致报告的数据,以及不一致的潜在来源。作为进一步理解肠道微生物群对 PD 影响的一步,我们讨论了肠道微生物群失调与对多巴胺替代治疗反应之间的关系,重点是左旋多巴代谢。我们得出的结论是,需要进一步的研究来确定 PD 患者中迄今为止观察到的肠道微生物群变化是疾病的原因,还是仅仅是与疾病相关的生活方式改变的结果。无论如何,迄今为止的研究强烈表明,微生物群的变化似乎对神经炎症的发病机制有影响。因此,PD 中的失调微生物群可能会影响疾病进程和对药物的反应,特别是左旋多巴。未来的研究将评估针对 PD 患者的微生物群定向治疗干预的影响。

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