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Iron-Induced Liver Injury: A Critical Reappraisal

Iron is implicated in the pathogenesis of a number of human liver diseases. Hereditary hemochromatosis is the classical example of a liver disease caused by iron, but iron is commonly believed to contribute to the progression of other forms of chronic liver disease such as hepatitis C infection and...

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Autores principales: Bloomer, Steven A., Brown, Kyle E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539962/
https://www.ncbi.nlm.nih.gov/pubmed/31052166
http://dx.doi.org/10.3390/ijms20092132
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author Bloomer, Steven A.
Brown, Kyle E.
author_facet Bloomer, Steven A.
Brown, Kyle E.
author_sort Bloomer, Steven A.
collection PubMed
description Iron is implicated in the pathogenesis of a number of human liver diseases. Hereditary hemochromatosis is the classical example of a liver disease caused by iron, but iron is commonly believed to contribute to the progression of other forms of chronic liver disease such as hepatitis C infection and nonalcoholic fatty liver disease. In this review, we present data from cell culture experiments, animal models, and clinical studies that address the hepatotoxicity of iron. These data demonstrate that iron overload is only weakly fibrogenic in animal models and rarely causes serious liver damage in humans, calling into question the concept that iron overload is an important cause of hepatotoxicity. In situations where iron is pathogenic, iron-induced liver damage may be potentiated by coexisting inflammation, with the resulting hepatocyte necrosis an important factor driving the fibrogenic response. Based on the foregoing evidence that iron is less hepatotoxic than is generally assumed, claims that assign a causal role to iron in liver injury in either animal models or human liver disease should be carefully evaluated.
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spelling pubmed-65399622019-06-04 Iron-Induced Liver Injury: A Critical Reappraisal Bloomer, Steven A. Brown, Kyle E. Int J Mol Sci Review Iron is implicated in the pathogenesis of a number of human liver diseases. Hereditary hemochromatosis is the classical example of a liver disease caused by iron, but iron is commonly believed to contribute to the progression of other forms of chronic liver disease such as hepatitis C infection and nonalcoholic fatty liver disease. In this review, we present data from cell culture experiments, animal models, and clinical studies that address the hepatotoxicity of iron. These data demonstrate that iron overload is only weakly fibrogenic in animal models and rarely causes serious liver damage in humans, calling into question the concept that iron overload is an important cause of hepatotoxicity. In situations where iron is pathogenic, iron-induced liver damage may be potentiated by coexisting inflammation, with the resulting hepatocyte necrosis an important factor driving the fibrogenic response. Based on the foregoing evidence that iron is less hepatotoxic than is generally assumed, claims that assign a causal role to iron in liver injury in either animal models or human liver disease should be carefully evaluated. MDPI 2019-04-30 /pmc/articles/PMC6539962/ /pubmed/31052166 http://dx.doi.org/10.3390/ijms20092132 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bloomer, Steven A.
Brown, Kyle E.
Iron-Induced Liver Injury: A Critical Reappraisal
title Iron-Induced Liver Injury: A Critical Reappraisal
title_full Iron-Induced Liver Injury: A Critical Reappraisal
title_fullStr Iron-Induced Liver Injury: A Critical Reappraisal
title_full_unstemmed Iron-Induced Liver Injury: A Critical Reappraisal
title_short Iron-Induced Liver Injury: A Critical Reappraisal
title_sort iron-induced liver injury: a critical reappraisal
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539962/
https://www.ncbi.nlm.nih.gov/pubmed/31052166
http://dx.doi.org/10.3390/ijms20092132
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