Alcohol dependence and alcoholic liver disease represent a major public health problem with substantial morbidity and mortality. By yet incompletely understood mechanisms, chronic alcohol abuse is associated with increased intestinal permeability and alterations of the gut microbiota composition, allowing bacterial components, bacteria, and metabolites to reach the portal and the systemic circulation. These gut-derived bacterial products are recognized by immune cells circulating in the blood or residing in remote organs such as the liver leading to the release of pro-inflammatory cytokines which are considered important mediators of the liver–gut–brain communication. Although circulating cytokines are likely not the sole factors involved, they can induce liver inflammation/damage and reach the central nervous system where they favor neuroinflammation which is associated with change in mood, cognition, and drinking behavior. In this review, the authors focus on the current evidence describing the changes that occur in the intestinal microbiota with chronic alcohol consumption in conjunction with intestinal barrier breakdown and inflammatory changes sustaining the concept of a gut–liver–brain axis in the pathophysiology of alcohol dependence and alcoholic liver disease.
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January 2018
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Oleic-acid-treated HepG2 cells immunostained for PGC-1α (PPARγ co-activator-1 α). In Clinical Science volume 132, issue 1, the results of work by Bernardi et al. include reporting that the protein TRAIL (TNF-related apoptosis inducing ligand) increases the expression of PGC-1α in HepG2 cells cultured with oleic acid. Overall, the article points to a potential therapeutic role for TRAIL against impaired glucose tolerance and non-alcoholic fatty liver disease; for details see pages 69–83.
Review Article|
January 19 2018
Intestinal dysbiosis and permeability: the yin and yang in alcohol dependence and alcoholic liver disease
Peter Stärkel;
1Laboratory of Hepato-Gastroenterology, Institute of Experimental and Clinical Research, Université catholique de Louvain, Brussels, Belgium
2Department of Hepato-Gastroenterology, Cliniques Universitaires St. Luc, Brussels, Belgium
Correspondence: Peter Stärkel ([email protected])
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Sophie Leclercq;
Sophie Leclercq
3Institute of Neuroscience, Université catholique de Louvain, Brussels, Belgium
4Metabolism and Nutrition Research Group, Louvain Drug Research Institute, Université catholique de Louvain, Brussels, Belgium
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Philippe de Timary;
Philippe de Timary
3Institute of Neuroscience, Université catholique de Louvain, Brussels, Belgium
5Department of Adult Psychiatry, Cliniques Universitaires St. Luc, Brussels, Belgium
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Bernd Schnabl
Bernd Schnabl
6Department of Medicine, University of California San Diego, La Jolla, CA, U.S.A.
7Department of Medicine, VA San Diego Healthcare System, San Diego, CA, U.S.A.
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Publisher: Portland Press Ltd
Received:
September 06 2017
Revision Received:
December 07 2017
Accepted:
December 19 2017
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© 2018 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society
2018
Clin Sci (Lond) (2018) 132 (2): 199–212.
Article history
Received:
September 06 2017
Revision Received:
December 07 2017
Accepted:
December 19 2017
Citation
Peter Stärkel, Sophie Leclercq, Philippe de Timary, Bernd Schnabl; Intestinal dysbiosis and permeability: the yin and yang in alcohol dependence and alcoholic liver disease. Clin Sci (Lond) 31 January 2018; 132 (2): 199–212. doi: https://doi.org/10.1042/CS20171055
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