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Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development
Chronic excessive alcohol use is a well-recognized risk factor for pancreatic dysfunction and pancreatitis development. Evidence from in vivo and in vitro studies indicates that the detrimental effects of alcohol on the pancreas are from the direct toxic effects of metabolites and byproducts of etha...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277520/ https://www.ncbi.nlm.nih.gov/pubmed/32349207 http://dx.doi.org/10.3390/biom10050669 |
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author | Rasineni, Karuna Srinivasan, Mukund P. Balamurugan, Appakalai N. Kaphalia, Bhupendra S. Wang, Shaogui Ding, Wen-Xing Pandol, Stephen J. Lugea, Aurelia Simon, Liz Molina, Patricia E. Gao, Peter Casey, Carol A. Osna, Natalia A. Kharbanda, Kusum K. |
author_facet | Rasineni, Karuna Srinivasan, Mukund P. Balamurugan, Appakalai N. Kaphalia, Bhupendra S. Wang, Shaogui Ding, Wen-Xing Pandol, Stephen J. Lugea, Aurelia Simon, Liz Molina, Patricia E. Gao, Peter Casey, Carol A. Osna, Natalia A. Kharbanda, Kusum K. |
author_sort | Rasineni, Karuna |
collection | PubMed |
description | Chronic excessive alcohol use is a well-recognized risk factor for pancreatic dysfunction and pancreatitis development. Evidence from in vivo and in vitro studies indicates that the detrimental effects of alcohol on the pancreas are from the direct toxic effects of metabolites and byproducts of ethanol metabolism such as reactive oxygen species. Pancreatic dysfunction and pancreatitis development are now increasingly thought to be multifactorial conditions, where alcohol, genetics, lifestyle, and infectious agents may determine the initiation and course of the disease. In this review, we first highlight the role of nonoxidative ethanol metabolism in the generation and accumulation of fatty acid ethyl esters (FAEEs) that cause multi-organellar dysfunction in the pancreas which ultimately leads to pancreatitis development. Further, we discuss how alcohol-mediated altered autophagy leads to the development of pancreatitis. We also provide insights into how alcohol interactions with other co-morbidities such as smoking or viral infections may negatively affect exocrine and endocrine pancreatic function. Finally, we present potential strategies to ameliorate organellar dysfunction which could attenuate pancreatic dysfunction and pancreatitis severity. |
format | Online Article Text |
id | pubmed-7277520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72775202020-06-12 Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development Rasineni, Karuna Srinivasan, Mukund P. Balamurugan, Appakalai N. Kaphalia, Bhupendra S. Wang, Shaogui Ding, Wen-Xing Pandol, Stephen J. Lugea, Aurelia Simon, Liz Molina, Patricia E. Gao, Peter Casey, Carol A. Osna, Natalia A. Kharbanda, Kusum K. Biomolecules Review Chronic excessive alcohol use is a well-recognized risk factor for pancreatic dysfunction and pancreatitis development. Evidence from in vivo and in vitro studies indicates that the detrimental effects of alcohol on the pancreas are from the direct toxic effects of metabolites and byproducts of ethanol metabolism such as reactive oxygen species. Pancreatic dysfunction and pancreatitis development are now increasingly thought to be multifactorial conditions, where alcohol, genetics, lifestyle, and infectious agents may determine the initiation and course of the disease. In this review, we first highlight the role of nonoxidative ethanol metabolism in the generation and accumulation of fatty acid ethyl esters (FAEEs) that cause multi-organellar dysfunction in the pancreas which ultimately leads to pancreatitis development. Further, we discuss how alcohol-mediated altered autophagy leads to the development of pancreatitis. We also provide insights into how alcohol interactions with other co-morbidities such as smoking or viral infections may negatively affect exocrine and endocrine pancreatic function. Finally, we present potential strategies to ameliorate organellar dysfunction which could attenuate pancreatic dysfunction and pancreatitis severity. MDPI 2020-04-27 /pmc/articles/PMC7277520/ /pubmed/32349207 http://dx.doi.org/10.3390/biom10050669 Text en © 2020 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 Rasineni, Karuna Srinivasan, Mukund P. Balamurugan, Appakalai N. Kaphalia, Bhupendra S. Wang, Shaogui Ding, Wen-Xing Pandol, Stephen J. Lugea, Aurelia Simon, Liz Molina, Patricia E. Gao, Peter Casey, Carol A. Osna, Natalia A. Kharbanda, Kusum K. Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development |
title | Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development |
title_full | Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development |
title_fullStr | Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development |
title_full_unstemmed | Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development |
title_short | Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development |
title_sort | recent advances in understanding the complexity of alcohol-induced pancreatic dysfunction and pancreatitis development |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277520/ https://www.ncbi.nlm.nih.gov/pubmed/32349207 http://dx.doi.org/10.3390/biom10050669 |
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