| Literature DB >> 34091018 |
Lacey B Sell1, Christina C Ramelow1, Hannah M Kohl1, Kristina Hoffman1, Jasleen K Bains1, William J Doyle1, Kevin D Strawn1, Theresa Hevrin1, Trevor O Kirby2, K Michael Gibson2, Jean-Baptiste Roullet2, Javier Ochoa-Repáraz3.
Abstract
Farnesol is a 15‑carbon organic isoprenol synthesized by plants and mammals with anti-oxidant, anti-inflammatory, and neuroprotective activities. We sought to determine whether farnesol treatment would result in protection against murine experimental autoimmune encephalomyelitis (EAE), a well-established model of multiple sclerosis (MS). We compared disease progression and severity in C57BL/6 mice treated orally with 100 mg/kg/day farnesol solubilized in corn oil to corn-oil treated and untreated EAE mice. Farnesol significantly delayed the onset of EAE (by ~2 days) and dramatically decreased disease severity (~80%) compared to controls. Disease protection by farnesol was associated with a significant reduction in spinal cord infiltration by monocytes-macrophages, dendritic cells, CD4+ T cells, and a significant change in gut microbiota composition, including a decrease in the Firmicutes:Bacteroidetes ratio. The study suggests FOL could protect MS patients against CNS inflammatory demyelination by partially modulating the gut microbiome composition.Entities:
Keywords: CNS inflammatory demyelination; EAE; Farnesol; Gut microbiome; Isoprenols
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Year: 2021 PMID: 34091018 PMCID: PMC8660955 DOI: 10.1016/j.clim.2021.108766
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969