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Microbiome-liver crosstalk: A multihit therapeutic target for liver disease
Liver disease has become a leading cause of death, particularly in the West, where it is attributed to more than two million deaths annually. The correlation between gut microbiota and liver disease is still not fully understood. However, it is well known that gut dysbiosis accompanied by a leaky gu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107210/ https://www.ncbi.nlm.nih.gov/pubmed/37077519 http://dx.doi.org/10.3748/wjg.v29.i11.1651 |
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author | Kirundi, Jorum Moghadamrad, Sheida Urbaniak, Camilla |
author_facet | Kirundi, Jorum Moghadamrad, Sheida Urbaniak, Camilla |
author_sort | Kirundi, Jorum |
collection | PubMed |
description | Liver disease has become a leading cause of death, particularly in the West, where it is attributed to more than two million deaths annually. The correlation between gut microbiota and liver disease is still not fully understood. However, it is well known that gut dysbiosis accompanied by a leaky gut causes an increase in lipopolysaccharides in circulation, which in turn evoke massive hepatic inflammation promoting liver cirrhosis. Microbial dysbiosis also leads to poor bile acid metabolism and low short-chain fatty acids, all of which exacerbate the inflammatory response of liver cells. Gut microbial homeostasis is maintained through intricate processes that ensure that commensal microbes adapt to the low oxygen potential of the gut and that they rapidly occupy all the intestinal niches, thus outcompeting any potential pathogens for available nutrients. The crosstalk between the gut microbiota and its metabolites also guarantee an intact gut barrier. These processes that protect against destabilization of gut microbes by potential entry of pathogenic bacteria are collectively called colonization resistance and are equally essential for liver health. In this review, we shall investigate how the mechanisms of colonization resistance influence the liver in health and disease and the microbial-liver crosstalk potential as therapeutic target areas. |
format | Online Article Text |
id | pubmed-10107210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-101072102023-04-18 Microbiome-liver crosstalk: A multihit therapeutic target for liver disease Kirundi, Jorum Moghadamrad, Sheida Urbaniak, Camilla World J Gastroenterol Review Liver disease has become a leading cause of death, particularly in the West, where it is attributed to more than two million deaths annually. The correlation between gut microbiota and liver disease is still not fully understood. However, it is well known that gut dysbiosis accompanied by a leaky gut causes an increase in lipopolysaccharides in circulation, which in turn evoke massive hepatic inflammation promoting liver cirrhosis. Microbial dysbiosis also leads to poor bile acid metabolism and low short-chain fatty acids, all of which exacerbate the inflammatory response of liver cells. Gut microbial homeostasis is maintained through intricate processes that ensure that commensal microbes adapt to the low oxygen potential of the gut and that they rapidly occupy all the intestinal niches, thus outcompeting any potential pathogens for available nutrients. The crosstalk between the gut microbiota and its metabolites also guarantee an intact gut barrier. These processes that protect against destabilization of gut microbes by potential entry of pathogenic bacteria are collectively called colonization resistance and are equally essential for liver health. In this review, we shall investigate how the mechanisms of colonization resistance influence the liver in health and disease and the microbial-liver crosstalk potential as therapeutic target areas. Baishideng Publishing Group Inc 2023-03-21 2023-03-21 /pmc/articles/PMC10107210/ /pubmed/37077519 http://dx.doi.org/10.3748/wjg.v29.i11.1651 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Review Kirundi, Jorum Moghadamrad, Sheida Urbaniak, Camilla Microbiome-liver crosstalk: A multihit therapeutic target for liver disease |
title | Microbiome-liver crosstalk: A multihit therapeutic target for liver disease |
title_full | Microbiome-liver crosstalk: A multihit therapeutic target for liver disease |
title_fullStr | Microbiome-liver crosstalk: A multihit therapeutic target for liver disease |
title_full_unstemmed | Microbiome-liver crosstalk: A multihit therapeutic target for liver disease |
title_short | Microbiome-liver crosstalk: A multihit therapeutic target for liver disease |
title_sort | microbiome-liver crosstalk: a multihit therapeutic target for liver disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107210/ https://www.ncbi.nlm.nih.gov/pubmed/37077519 http://dx.doi.org/10.3748/wjg.v29.i11.1651 |
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