| Literature DB >> 29874567 |
Francesca Cignarella1, Claudia Cantoni1, Laura Ghezzi2, Amber Salter3, Yair Dorsett4, Lei Chen4, Daniel Phillips4, George M Weinstock4, Luigi Fontana5, Anne H Cross6, Yanjiao Zhou7, Laura Piccio8.
Abstract
Multiple sclerosis (MS) is more common in western countries with diet being a potential contributing factor. Here we show that intermittent fasting (IF) ameliorated clinical course and pathology of the MS model, experimental autoimmune encephalomyelitis (EAE). IF led to increased gut bacteria richness, enrichment of the Lactobacillaceae, Bacteroidaceae, and Prevotellaceae families and enhanced antioxidative microbial metabolic pathways. IF altered T cells in the gut with a reduction of IL-17 producing T cells and an increase in regulatory T cells. Fecal microbiome transplantation from mice on IF ameliorated EAE in immunized recipient mice on a normal diet, suggesting that IF effects are at least partially mediated by the gut flora. In a pilot clinical trial in MS patients, intermittent energy restriction altered blood adipokines and the gut flora resembling protective changes observed in mice. In conclusion, IF has potent immunomodulatory effects that are at least partially mediated by the gut microbiome.Entities:
Keywords: diet; experimental autoimmune encephalomyelitis; gut microbiota; intermittent fasting; multiple sclerosis
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Year: 2018 PMID: 29874567 PMCID: PMC6460288 DOI: 10.1016/j.cmet.2018.05.006
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287