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恢复与多发性硬化相关的肠道吲哚代谢物失衡可促进髓鞘再生并抑制神经炎症。

Restoring the Multiple Sclerosis Associated Imbalance of Gut Indole Metabolites Promotes Remyelination and Suppresses Neuroinflammation.

作者信息

Jank Larissa, Singh Saumitra S, Lee Judy, Dhukhwa Asmita, Siavoshi Fatemeh, Joshi Deepika, Minney Veronica, Gupta Kanak, Ghimire Sudeep, Deme Pragney, Schoeps Vinicius A, Soman Karthik, Ladakis Dimitrios, Smith Matthew, Borkowski Kamil, Newman John, Baranzini Sergio E, Waubant Emmanuelle L, Fitzgerald Kathryn C, Mangalam Ashutosh, Haughey Norman, Kornberg Michael, Chamling Xitiz, Calabresi Peter A, Bhargava Pavan

机构信息

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

bioRxiv. 2025 Jan 13:2024.10.27.620437. doi: 10.1101/2024.10.27.620437.

Abstract

In multiple sclerosis (MS) the circulating metabolome is dysregulated, with indole lactate (ILA) being one of the most significantly reduced metabolites. We demonstrate that oral supplementation of ILA impacts key MS disease processes in two preclinical models. ILA reduces neuroinflammation by dampening immune cell activation as well as infiltration; and promotes remyelination and oligodendrocyte differentiation through the aryl hydrocarbon receptor (AhR). Supplementation of ILA, a reductive indole metabolite, restores the gut microbiome's oxidative/reductive metabolic balance by lowering circulating indole acetate (IAA), an oxidative indole metabolite, that blocks remyelination and oligodendrocyte maturation. The ILA-induced reduction in circulating IAA is linked to changes in IAA-producing gut microbiota taxa and pathways that are also dysregulated in MS. Notably, a lower ILA:IAA ratio correlates with worse MS outcomes. Overall, these findings identify ILA as a potential anti-inflammatory remyelinating agent and provide insights into the role of gut dysbiosis-related metabolic alterations in MS progression.

摘要

在多发性硬化症(MS)中,循环代谢组发生失调,吲哚乳酸(ILA)是其中显著减少的代谢物之一。我们证明,在两种临床前模型中,口服补充ILA会影响MS的关键疾病进程。ILA通过抑制免疫细胞激活和浸润来减轻神经炎症;并通过芳烃受体(AhR)促进髓鞘再生和少突胶质细胞分化。补充ILA这种还原性吲哚代谢物,可通过降低循环中的吲哚乙酸(IAA,一种氧化性吲哚代谢物,会阻碍髓鞘再生和少突胶质细胞成熟)来恢复肠道微生物群的氧化/还原代谢平衡。ILA诱导循环中IAA减少与产生IAA的肠道微生物群分类群和途径的变化有关,这些在MS中也失调。值得注意的是,较低的ILA:IAA比值与较差的MS预后相关。总体而言,这些发现确定ILA为一种潜在的抗炎性髓鞘再生剂,并为肠道生态失调相关代谢改变在MS进展中的作用提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9304/11730895/770c64a288aa/nihpp-2024.10.27.620437v2-f0001.jpg

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