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      The Brain-Gut-Microbiome Axis

      review-article
      , , ,
      Cellular and Molecular Gastroenterology and Hepatology
      Elsevier
      Serotonin, Stress, Irritable Bowel Syndrome, Intestinal Permeability, ANS, autonomic nervous system, ASD, autism spectrum disorder, BBB, blood-brain barrier, BGM, brain-gut-microbiome, CNS, central nervous system, ECC, enterochromaffin cell, EEC, enteroendocrine cell, FFAR, free fatty acid receptor, FGF, fibroblast growth factor, 5-HT, serotonin, FXR, farnesoid X receptor, GF, germ-free, GI, gastrointestinal, GLP-1, glucagon-like peptide-1, GPR, G-protein–coupled receptor, IBS, irritable bowel syndrome, LPS, lipopolysaccharide, SCFA, short-chain fatty acid, SPF, specific-pathogen-free, TGR5, G protein-coupled bile acid receptor, Trp, tryptophan, 2BA, secondary bile acid

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          Abstract

          Preclinical and clinical studies have shown bidirectional interactions within the brain-gut-microbiome axis. Gut microbes communicate to the central nervous system through at least 3 parallel and interacting channels involving nervous, endocrine, and immune signaling mechanisms. The brain can affect the community structure and function of the gut microbiota through the autonomic nervous system, by modulating regional gut motility, intestinal transit and secretion, and gut permeability, and potentially through the luminal secretion of hormones that directly modulate microbial gene expression. A systems biological model is proposed that posits circular communication loops amid the brain, gut, and gut microbiome, and in which perturbation at any level can propagate dysregulation throughout the circuit. A series of largely preclinical observations implicates alterations in brain-gut-microbiome communication in the pathogenesis and pathophysiology of irritable bowel syndrome, obesity, and several psychiatric and neurologic disorders. Continued research holds the promise of identifying novel therapeutic targets and developing treatment strategies to address some of the most debilitating, costly, and poorly understood diseases.

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          Most cited references94

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          Recognition of commensal microflora by toll-like receptors is required for intestinal homeostasis.

          Toll-like receptors (TLRs) play a crucial role in host defense against microbial infection. The microbial ligands recognized by TLRs are not unique to pathogens, however, and are produced by both pathogenic and commensal microorganisms. It is thought that an inflammatory response to commensal bacteria is avoided due to sequestration of microflora by surface epithelia. Here, we show that commensal bacteria are recognized by TLRs under normal steady-state conditions, and this interaction plays a crucial role in the maintenance of intestinal epithelial homeostasis. Furthermore, we find that activation of TLRs by commensal microflora is critical for the protection against gut injury and associated mortality. These findings reveal a novel function of TLRs-control of intestinal epithelial homeostasis and protection from injury-and provide a new perspective on the evolution of host-microbial interactions.
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            Short-chain fatty acids and human colonic function: roles of resistant starch and nonstarch polysaccharides.

            Resistant starch (RS) is starch and products of its small intestinal digestion that enter the large bowel. It occurs for various reasons including chemical structure, cooking of food, chemical modification, and food mastication. Human colonic bacteria ferment RS and nonstarch polysaccharides (NSP; major components of dietary fiber) to short-chain fatty acids (SCFA), mainly acetate, propionate, and butyrate. SCFA stimulate colonic blood flow and fluid and electrolyte uptake. Butyrate is a preferred substrate for colonocytes and appears to promote a normal phenotype in these cells. Fermentation of some RS types favors butyrate production. Measurement of colonic fermentation in humans is difficult, and indirect measures (e.g., fecal samples) or animal models have been used. Of the latter, rodents appear to be of limited value, and pigs or dogs are preferable. RS is less effective than NSP in stool bulking, but epidemiological data suggest that it is more protective against colorectal cancer, possibly via butyrate. RS is a prebiotic, but knowledge of its other interactions with the microflora is limited. The contribution of RS to fermentation and colonic physiology seems to be greater than that of NSP. However, the lack of a generally accepted analytical procedure that accommodates the major influences on RS means this is yet to be established.
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              The Toll-like receptor 2 pathway establishes colonization by a commensal of the human microbiota.

              Mucosal surfaces constantly encounter microbes. Toll-like receptors (TLRs) mediate recognition of microbial patterns to eliminate pathogens. By contrast, we demonstrate that the prominent gut commensal Bacteroides fragilis activates the TLR pathway to establish host-microbial symbiosis. TLR2 on CD4(+) T cells is required for B. fragilis colonization of a unique mucosal niche in mice during homeostasis. A symbiosis factor (PSA, polysaccharide A) of B. fragilis signals through TLR2 directly on Foxp3(+) regulatory T cells to promote immunologic tolerance. B. fragilis lacking PSA is unable to restrain T helper 17 cell responses and is defective in niche-specific mucosal colonization. Therefore, commensal bacteria exploit the TLR pathway to actively suppress immunity. We propose that the immune system can discriminate between pathogens and the microbiota through recognition of symbiotic bacterial molecules in a process that engenders commensal colonization.
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                Author and article information

                Contributors
                Journal
                Cell Mol Gastroenterol Hepatol
                Cell Mol Gastroenterol Hepatol
                Cellular and Molecular Gastroenterology and Hepatology
                Elsevier
                2352-345X
                12 April 2018
                2018
                12 April 2018
                : 6
                : 2
                : 133-148
                Affiliations
                [1]G. Oppenheimer Center for Neurobiology of Stress and Resilience, Vatche and Tamar Manoukian Division of Digestive Diseases, Microbiome Center, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California
                Author notes
                [] Correspondence Address correspondence to: Emeran A. Mayer, MD, G. Oppenheimer Center for Neurobiology of Stress and Resilience, University of California at Los Angeles, MC737818-10833 Le Conte Avenue, Los Angeles, California 90095-7378. fax: (310) 825-1919. emayer@ 123456ucla.edu
                Article
                S2352-345X(18)30060-2
                10.1016/j.jcmgh.2018.04.003
                6047317
                30023410
                2246c9a0-05bd-4f54-876f-c0d0282aed89
                © 2018 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 19 November 2017
                : 4 April 2018
                Categories
                Review

                serotonin,stress,irritable bowel syndrome,intestinal permeability,ans, autonomic nervous system,asd, autism spectrum disorder,bbb, blood-brain barrier,bgm, brain-gut-microbiome,cns, central nervous system,ecc, enterochromaffin cell,eec, enteroendocrine cell,ffar, free fatty acid receptor,fgf, fibroblast growth factor,5-ht, serotonin,fxr, farnesoid x receptor,gf, germ-free,gi, gastrointestinal,glp-1, glucagon-like peptide-1,gpr, g-protein–coupled receptor,ibs, irritable bowel syndrome,lps, lipopolysaccharide,scfa, short-chain fatty acid,spf, specific-pathogen-free,tgr5, g protein-coupled bile acid receptor,trp, tryptophan,2ba, secondary bile acid

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