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Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders
The emerging links between our gut microbiome and the central nervous system (CNS) are regarded as a paradigm shift in neuroscience with possible implications for not only understanding the pathophysiology of stress-related psychiatric disorders, but also their treatment. Thus the gut microbiome and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604320/ https://www.ncbi.nlm.nih.gov/pubmed/26528128 http://dx.doi.org/10.3389/fncel.2015.00392 |
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author | Kelly, John R. Kennedy, Paul J. Cryan, John F. Dinan, Timothy G. Clarke, Gerard Hyland, Niall P. |
author_facet | Kelly, John R. Kennedy, Paul J. Cryan, John F. Dinan, Timothy G. Clarke, Gerard Hyland, Niall P. |
author_sort | Kelly, John R. |
collection | PubMed |
description | The emerging links between our gut microbiome and the central nervous system (CNS) are regarded as a paradigm shift in neuroscience with possible implications for not only understanding the pathophysiology of stress-related psychiatric disorders, but also their treatment. Thus the gut microbiome and its influence on host barrier function is positioned to be a critical node within the brain-gut axis. Mounting preclinical evidence broadly suggests that the gut microbiota can modulate brain development, function and behavior by immune, endocrine and neural pathways of the brain-gut-microbiota axis. Detailed mechanistic insights explaining these specific interactions are currently underdeveloped. However, the concept that a “leaky gut” may facilitate communication between the microbiota and these key signaling pathways has gained traction. Deficits in intestinal permeability may underpin the chronic low-grade inflammation observed in disorders such as depression and the gut microbiome plays a critical role in regulating intestinal permeability. In this review we will discuss the possible role played by the gut microbiota in maintaining intestinal barrier function and the CNS consequences when it becomes disrupted. We will draw on both clinical and preclinical evidence to support this concept as well as the key features of the gut microbiota which are necessary for normal intestinal barrier function. |
format | Online Article Text |
id | pubmed-4604320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46043202015-11-02 Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders Kelly, John R. Kennedy, Paul J. Cryan, John F. Dinan, Timothy G. Clarke, Gerard Hyland, Niall P. Front Cell Neurosci Neuroscience The emerging links between our gut microbiome and the central nervous system (CNS) are regarded as a paradigm shift in neuroscience with possible implications for not only understanding the pathophysiology of stress-related psychiatric disorders, but also their treatment. Thus the gut microbiome and its influence on host barrier function is positioned to be a critical node within the brain-gut axis. Mounting preclinical evidence broadly suggests that the gut microbiota can modulate brain development, function and behavior by immune, endocrine and neural pathways of the brain-gut-microbiota axis. Detailed mechanistic insights explaining these specific interactions are currently underdeveloped. However, the concept that a “leaky gut” may facilitate communication between the microbiota and these key signaling pathways has gained traction. Deficits in intestinal permeability may underpin the chronic low-grade inflammation observed in disorders such as depression and the gut microbiome plays a critical role in regulating intestinal permeability. In this review we will discuss the possible role played by the gut microbiota in maintaining intestinal barrier function and the CNS consequences when it becomes disrupted. We will draw on both clinical and preclinical evidence to support this concept as well as the key features of the gut microbiota which are necessary for normal intestinal barrier function. Frontiers Media S.A. 2015-10-14 /pmc/articles/PMC4604320/ /pubmed/26528128 http://dx.doi.org/10.3389/fncel.2015.00392 Text en Copyright © 2015 Kelly, Kennedy, Cryan, Dinan, Clarke and Hyland. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kelly, John R. Kennedy, Paul J. Cryan, John F. Dinan, Timothy G. Clarke, Gerard Hyland, Niall P. Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
title | Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
title_full | Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
title_fullStr | Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
title_full_unstemmed | Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
title_short | Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
title_sort | breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604320/ https://www.ncbi.nlm.nih.gov/pubmed/26528128 http://dx.doi.org/10.3389/fncel.2015.00392 |
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