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The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential
Sepsis is a potentially fatal condition caused by dysregulation of the body's immune response to an infection. Sepsis-induced liver injury is considered a strong independent prognosticator of death in the critical care unit, and there is anatomic and accumulating epidemiologic evidence that dem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277879/ https://www.ncbi.nlm.nih.gov/pubmed/35831877 http://dx.doi.org/10.1186/s13054-022-04090-1 |
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author | Zhang, Xue Liu, Hong Hashimoto, Kenji Yuan, Shiying Zhang, Jiancheng |
author_facet | Zhang, Xue Liu, Hong Hashimoto, Kenji Yuan, Shiying Zhang, Jiancheng |
author_sort | Zhang, Xue |
collection | PubMed |
description | Sepsis is a potentially fatal condition caused by dysregulation of the body's immune response to an infection. Sepsis-induced liver injury is considered a strong independent prognosticator of death in the critical care unit, and there is anatomic and accumulating epidemiologic evidence that demonstrates intimate cross talk between the gut and the liver. Intestinal barrier disruption and gut microbiota dysbiosis during sepsis result in translocation of intestinal pathogen-associated molecular patterns and damage-associated molecular patterns into the liver and systemic circulation. The liver is essential for regulating immune defense during systemic infections via mechanisms such as bacterial clearance, lipopolysaccharide detoxification, cytokine and acute-phase protein release, and inflammation metabolic regulation. When an inappropriate immune response or overwhelming inflammation occurs in the liver, the impaired capacity for pathogen clearance and hepatic metabolic disturbance can result in further impairment of the intestinal barrier and increased disruption of the composition and diversity of the gut microbiota. Therefore, interaction between the gut and liver is a potential therapeutic target. This review outlines the intimate gut–liver cross talk (gut–liver axis) in sepsis. |
format | Online Article Text |
id | pubmed-9277879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92778792022-07-14 The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential Zhang, Xue Liu, Hong Hashimoto, Kenji Yuan, Shiying Zhang, Jiancheng Crit Care Review Sepsis is a potentially fatal condition caused by dysregulation of the body's immune response to an infection. Sepsis-induced liver injury is considered a strong independent prognosticator of death in the critical care unit, and there is anatomic and accumulating epidemiologic evidence that demonstrates intimate cross talk between the gut and the liver. Intestinal barrier disruption and gut microbiota dysbiosis during sepsis result in translocation of intestinal pathogen-associated molecular patterns and damage-associated molecular patterns into the liver and systemic circulation. The liver is essential for regulating immune defense during systemic infections via mechanisms such as bacterial clearance, lipopolysaccharide detoxification, cytokine and acute-phase protein release, and inflammation metabolic regulation. When an inappropriate immune response or overwhelming inflammation occurs in the liver, the impaired capacity for pathogen clearance and hepatic metabolic disturbance can result in further impairment of the intestinal barrier and increased disruption of the composition and diversity of the gut microbiota. Therefore, interaction between the gut and liver is a potential therapeutic target. This review outlines the intimate gut–liver cross talk (gut–liver axis) in sepsis. BioMed Central 2022-07-13 /pmc/articles/PMC9277879/ /pubmed/35831877 http://dx.doi.org/10.1186/s13054-022-04090-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Zhang, Xue Liu, Hong Hashimoto, Kenji Yuan, Shiying Zhang, Jiancheng The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
title | The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
title_full | The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
title_fullStr | The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
title_full_unstemmed | The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
title_short | The gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
title_sort | gut–liver axis in sepsis: interaction mechanisms and therapeutic potential |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277879/ https://www.ncbi.nlm.nih.gov/pubmed/35831877 http://dx.doi.org/10.1186/s13054-022-04090-1 |
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