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Acute Alcohol-Induced Liver Injury

Alcohol consumption is customary in most cultures and alcohol abuse is common worldwide. For example, more than 50% of Americans consume alcohol, with an estimated 23.1% of Americans participating in heavy and/or binge drinking at least once a month. A safe and effective therapy for alcoholic liver...

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Autores principales: Massey, Veronica L., Arteel, Gavin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372892/
https://www.ncbi.nlm.nih.gov/pubmed/22701432
http://dx.doi.org/10.3389/fphys.2012.00193
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author Massey, Veronica L.
Arteel, Gavin E.
author_facet Massey, Veronica L.
Arteel, Gavin E.
author_sort Massey, Veronica L.
collection PubMed
description Alcohol consumption is customary in most cultures and alcohol abuse is common worldwide. For example, more than 50% of Americans consume alcohol, with an estimated 23.1% of Americans participating in heavy and/or binge drinking at least once a month. A safe and effective therapy for alcoholic liver disease (ALD) in humans is still elusive, despite significant advances in our understanding of how the disease is initiated and progresses. It is now clear that acute alcohol binges not only can be acutely toxic to the liver, but also can contribute to the chronicity of ALD. Potential mechanisms by which acute alcohol causes damage include steatosis, dysregulated immunity and inflammation, and altered gut permeability. Recent interest in modeling acute alcohol exposure has yielded new insights into potential mechanisms of acute injury, which also may well be relevant for chronic ALD. Recent work by this group on the role of PAI-1 and fibrin metabolism in mediating acute alcohol-induced liver damage serve as an example of possible new targets that may be useful for alcohol abuse, be it acute or chronic.
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spelling pubmed-33728922012-06-14 Acute Alcohol-Induced Liver Injury Massey, Veronica L. Arteel, Gavin E. Front Physiol Physiology Alcohol consumption is customary in most cultures and alcohol abuse is common worldwide. For example, more than 50% of Americans consume alcohol, with an estimated 23.1% of Americans participating in heavy and/or binge drinking at least once a month. A safe and effective therapy for alcoholic liver disease (ALD) in humans is still elusive, despite significant advances in our understanding of how the disease is initiated and progresses. It is now clear that acute alcohol binges not only can be acutely toxic to the liver, but also can contribute to the chronicity of ALD. Potential mechanisms by which acute alcohol causes damage include steatosis, dysregulated immunity and inflammation, and altered gut permeability. Recent interest in modeling acute alcohol exposure has yielded new insights into potential mechanisms of acute injury, which also may well be relevant for chronic ALD. Recent work by this group on the role of PAI-1 and fibrin metabolism in mediating acute alcohol-induced liver damage serve as an example of possible new targets that may be useful for alcohol abuse, be it acute or chronic. Frontiers Research Foundation 2012-06-12 /pmc/articles/PMC3372892/ /pubmed/22701432 http://dx.doi.org/10.3389/fphys.2012.00193 Text en Copyright © 2012 Massey and Arteel. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Physiology
Massey, Veronica L.
Arteel, Gavin E.
Acute Alcohol-Induced Liver Injury
title Acute Alcohol-Induced Liver Injury
title_full Acute Alcohol-Induced Liver Injury
title_fullStr Acute Alcohol-Induced Liver Injury
title_full_unstemmed Acute Alcohol-Induced Liver Injury
title_short Acute Alcohol-Induced Liver Injury
title_sort acute alcohol-induced liver injury
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372892/
https://www.ncbi.nlm.nih.gov/pubmed/22701432
http://dx.doi.org/10.3389/fphys.2012.00193
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