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Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity
The sympathetic nervous system and the immune system are responsible for producing neurotransmitters and cytokines that interact by binding to receptors; due to this, there is communication between these systems. Liver immune cells and nerve fibres are systematically distributed in the liver, and th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970206/ https://www.ncbi.nlm.nih.gov/pubmed/36826975 http://dx.doi.org/10.1080/07853890.2022.2164047 |
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author | Medina Pizaño, Mariana Yazmin Loera Arias, María de Jesús Montes de Oca Luna, Roberto Saucedo Cárdenas, Odila Ventura Juárez, Javier Muñoz Ortega, Martin Humberto |
author_facet | Medina Pizaño, Mariana Yazmin Loera Arias, María de Jesús Montes de Oca Luna, Roberto Saucedo Cárdenas, Odila Ventura Juárez, Javier Muñoz Ortega, Martin Humberto |
author_sort | Medina Pizaño, Mariana Yazmin |
collection | PubMed |
description | The sympathetic nervous system and the immune system are responsible for producing neurotransmitters and cytokines that interact by binding to receptors; due to this, there is communication between these systems. Liver immune cells and nerve fibres are systematically distributed in the liver, and the partial overlap of both patterns may favour interactions between certain elements. Dendritic cells are attached to fibroblasts, and nerve fibres are connected via the dendritic cell-fibroblast complex. Receptors for most neuroactive substances, such as catecholamines, have been discovered on dendritic cells. The sympathetic nervous system regulates hepatic fibrosis through sympathetic fibres and adrenaline from the adrenal glands through the blood. When there is liver damage, the sympathetic nervous system is activated locally and systemically through proinflammatory cytokines that induce the production of epinephrine and norepinephrine. These neurotransmitters bind to cells through α-adrenergic receptors, triggering a cellular response that secretes inflammatory factors that stimulate and activate hepatic stellate cells. Hepatic stellate cells are key in the fibrotic process. They initiate the overproduction of extracellular matrix components in an active state that progresses from fibrosis to liver cirrhosis. It has also been shown that they can be directly activated by norepinephrine. Alpha and beta adrenoblockers, such as carvedilol, prazosin, and doxazosin, have recently been used to reverse CCl(4)-induced liver cirrhosis in rodent and murine models. KEY MESSAGES: Neurotransmitters from the sympathetic nervous system activate and increase the proliferation of hepatic stellate cells. Hepatic fibrosis and cirrhosis treatment might depend on neurotransmitter and hepatic nervous system regulation. Strategies to reduce hepatic stellate cell activation and fibrosis are based on experimentation with α-adrenoblockers. |
format | Online Article Text |
id | pubmed-9970206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-99702062023-02-28 Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity Medina Pizaño, Mariana Yazmin Loera Arias, María de Jesús Montes de Oca Luna, Roberto Saucedo Cárdenas, Odila Ventura Juárez, Javier Muñoz Ortega, Martin Humberto Ann Med Gastroenterology & Hepatology The sympathetic nervous system and the immune system are responsible for producing neurotransmitters and cytokines that interact by binding to receptors; due to this, there is communication between these systems. Liver immune cells and nerve fibres are systematically distributed in the liver, and the partial overlap of both patterns may favour interactions between certain elements. Dendritic cells are attached to fibroblasts, and nerve fibres are connected via the dendritic cell-fibroblast complex. Receptors for most neuroactive substances, such as catecholamines, have been discovered on dendritic cells. The sympathetic nervous system regulates hepatic fibrosis through sympathetic fibres and adrenaline from the adrenal glands through the blood. When there is liver damage, the sympathetic nervous system is activated locally and systemically through proinflammatory cytokines that induce the production of epinephrine and norepinephrine. These neurotransmitters bind to cells through α-adrenergic receptors, triggering a cellular response that secretes inflammatory factors that stimulate and activate hepatic stellate cells. Hepatic stellate cells are key in the fibrotic process. They initiate the overproduction of extracellular matrix components in an active state that progresses from fibrosis to liver cirrhosis. It has also been shown that they can be directly activated by norepinephrine. Alpha and beta adrenoblockers, such as carvedilol, prazosin, and doxazosin, have recently been used to reverse CCl(4)-induced liver cirrhosis in rodent and murine models. KEY MESSAGES: Neurotransmitters from the sympathetic nervous system activate and increase the proliferation of hepatic stellate cells. Hepatic fibrosis and cirrhosis treatment might depend on neurotransmitter and hepatic nervous system regulation. Strategies to reduce hepatic stellate cell activation and fibrosis are based on experimentation with α-adrenoblockers. Taylor & Francis 2023-02-24 /pmc/articles/PMC9970206/ /pubmed/36826975 http://dx.doi.org/10.1080/07853890.2022.2164047 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gastroenterology & Hepatology Medina Pizaño, Mariana Yazmin Loera Arias, María de Jesús Montes de Oca Luna, Roberto Saucedo Cárdenas, Odila Ventura Juárez, Javier Muñoz Ortega, Martin Humberto Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
title | Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
title_full | Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
title_fullStr | Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
title_full_unstemmed | Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
title_short | Neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
title_sort | neuroimmunomodulation of adrenoblockers during liver cirrhosis: modulation of hepatic stellate cell activity |
topic | Gastroenterology & Hepatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970206/ https://www.ncbi.nlm.nih.gov/pubmed/36826975 http://dx.doi.org/10.1080/07853890.2022.2164047 |
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