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多发性硬化症及动物模型中的肠道微生物群

Gut microbiota in multiple sclerosis and animal models.

作者信息

Schumacher Sean M, Doyle William J, Hill Kristina, Ochoa-Repáraz Javier

机构信息

Department of Biological Sciences, Boise State University, ID, USA.

出版信息

FEBS J. 2025 Mar;292(6):1330-1356. doi: 10.1111/febs.17161. Epub 2024 May 30.

DOI:10.1111/febs.17161
PMID:38817090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11607183/
Abstract

Multiple sclerosis (MS) is a chronic central nervous system (CNS) neurodegenerative and neuroinflammatory disease marked by a host immune reaction that targets and destroys the neuronal myelin sheath. MS and correlating animal disease models show comorbidities, including intestinal barrier disruption and alterations of the commensal microbiome. It is accepted that diet plays a crucial role in shaping the microbiota composition and overall gastrointestinal (GI) tract health, suggesting an interplay between nutrition and neuroinflammation via the gut-brain axis. Unfortunately, poor host health and diet lead to microbiota modifications that could lead to significant responses in the host, including inflammation and neurobehavioral changes. Beneficial microbial metabolites are essential for host homeostasis and inflammation control. This review will highlight the importance of the gut microbiota in the context of host inflammatory responses in MS and MS animal models. Additionally, microbial community restoration and how it affects MS and GI barrier integrity will be discussed.

摘要

多发性硬化症(MS)是一种慢性中枢神经系统(CNS)神经退行性和神经炎症性疾病,其特征是宿主免疫反应靶向并破坏神经元髓鞘。MS及相关动物疾病模型显示出合并症,包括肠道屏障破坏和共生微生物群的改变。人们认为饮食在塑造微生物群组成和整体胃肠道(GI)健康方面起着至关重要的作用,这表明营养与神经炎症之间通过肠-脑轴相互作用。不幸的是,宿主健康状况不佳和饮食会导致微生物群改变,进而可能在宿主中引发显著反应,包括炎症和神经行为变化。有益的微生物代谢产物对于宿主内环境稳态和炎症控制至关重要。本综述将强调肠道微生物群在MS及MS动物模型宿主炎症反应中的重要性。此外,还将讨论微生物群落恢复及其对MS和胃肠道屏障完整性的影响。

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BMJ. 2024 Feb 28;384:e077310. doi: 10.1136/bmj-2023-077310.
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Metagenomic signatures reveal the key role of phloretin in amelioration of gut dysbiosis attributed to metabolic dysfunction-associated fatty liver disease by time-dependent modulation of gut microbiome.宏基因组特征揭示了根皮素通过对肠道微生物群的时间依赖性调节,在改善代谢功能障碍相关脂肪性肝病所致肠道菌群失调中发挥的关键作用。
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