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      Microbiome—The Missing Link in the Gut-Brain Axis: Focus on Its Role in Gastrointestinal and Mental Health

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          Abstract

          The central nervous system (CNS) and the human gastrointestinal (GI) tract communicate through the gut-brain axis (GBA). Such communication is bi-directional and involves neuronal, endocrine, and immunological mechanisms. There is mounting data that gut microbiota is the source of a number of neuroactive and immunocompetent substances, which shape the structure and function of brain regions involved in the control of emotions, cognition, and physical activity. Most GI diseases are associated with altered transmission within the GBA that are influenced by both genetic and environmental factors. Current treatment protocols for GI and non-GI disorders may positively or adversely affect the composition of intestinal microbiota with a diverse impact on therapeutic outcome(s). Alterations of gut microbiota have been associated with mood and depressive disorders. Moreover, mental health is frequently affected in GI and non-GI diseases. Deregulation of the GBA may constitute a grip point for the development of diagnostic tools and personalized microbiota-based therapy. For example, next generation sequencing (NGS) offers detailed analysis of microbiome footprints in patients with mental and GI disorders. Elucidating the role of stem cell–host microbiome cross talks in tissues in GBA disorders might lead to the development of next generation diagnostics and therapeutics. Psychobiotics are a new class of beneficial bacteria with documented efficacy for the treatment of GBA disorders. Novel therapies interfering with small molecules involved in adult stem cell trafficking are on the horizon.

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          Most cited references115

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          The Lancet Commission on global mental health and sustainable development

          The Lancet, 392(10157), 1553-1598
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            A gut-vascular barrier controls the systemic dissemination of bacteria.

            In healthy individuals, the intestinal microbiota cannot access the liver, spleen, or other peripheral tissues. Some pathogenic bacteria can reach these sites, however, and can induce a systemic immune response. How such compartmentalization is achieved is unknown. We identify a gut-vascular barrier (GVB) in mice and humans that controls the translocation of antigens into the blood stream and prohibits entry of the microbiota. Salmonella typhimurium can penetrate the GVB in a manner dependent on its pathogenicity island (Spi) 2-encoded type III secretion system and on decreased β-catenin-dependent signaling in gut endothelial cells. The GVB is modified in celiac disease patients with elevated serum transaminases, which indicates that GVB dismantling may be responsible for liver damage in these patients. Understanding the GVB may provide new insights into the regulation of the gut-liver axis.
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              Possible association of Bifidobacterium and Lactobacillus in the gut microbiota of patients with major depressive disorder.

              Bifidobacterium and Lactobacillus in the gut have been suggested to have a beneficial effect on stress response and depressive disorder. We examined whether these bacterial counts are reduced in patients with major depressive disorder (MDD) than in healthy controls.
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                Author and article information

                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                07 December 2018
                December 2018
                : 7
                : 12
                : 521
                Affiliations
                [1 ]Department of Biochemistry and Human Nutrition, Pomeranian Medical University in Szczecin, 71-460 Szczecin, Poland; karzyd@ 123456pum.edu.pl (K.S.-Z.); igorloniewski@ 123456sanum.com.pl (I.L.)
                [2 ]Department of Gastroenterology, Pomeranian Medical University, 71-252 Szczecin, Poland
                [3 ]Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin, 13353 Berlin, Germany; agata.misera@ 123456charite.de
                [4 ]Endoscopy Unit, The Royal Infirmary of Edinburgh, EH16 4SA Edinburgh, UK; akoulaouzidis@ 123456hotmail.com
                Author notes
                [* ]Correspondence: marlicz@ 123456hotmail.com ; Tel.: +48-(91)-425-32-31
                Author information
                https://orcid.org/0000-0002-3430-9079
                https://orcid.org/0000-0002-2649-5967
                https://orcid.org/0000-0002-2248-489X
                Article
                jcm-07-00521
                10.3390/jcm7120521
                6306769
                30544486
                99393790-ed0f-4abd-811f-b0501945b07c
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 23 October 2018
                : 05 December 2018
                Categories
                Review

                gut brain axis,microbiota,functional gastrointestinal disorders,inflammatory bowel disease (ibd),adult stem cells

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