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...

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Main Authors: Karuna Rasineni, Mukund P. Srinivasan, Appakalai N. Balamurugan, Bhupendra S. Kaphalia, Shaogui Wang, Wen-Xing Ding, Stephen J. Pandol, Aurelia Lugea, Liz Simon, Patricia E. Molina, Peter Gao, Carol A. Casey, Natalia A. Osna, Kusum K. Kharbanda
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/10/5/669
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spelling doaj-19878899bdaf4365ad8e7fe4283c888d2020-11-25T03:47:01ZengMDPI AGBiomolecules2218-273X2020-04-011066966910.3390/biom10050669Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis DevelopmentKaruna Rasineni0Mukund P. Srinivasan1Appakalai N. Balamurugan2Bhupendra S. Kaphalia3Shaogui Wang4Wen-Xing Ding5Stephen J. Pandol6Aurelia Lugea7Liz Simon8Patricia E. Molina9Peter Gao10Carol A. Casey11Natalia A. Osna12Kusum K. Kharbanda13Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USADepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0419, USADivision of Pediatric General and Thoracic Surgery, Cincinnati Children’s Hospital Medical Center, Department of Surgery, University of Cincinnati, Cincinnati, OH 45229, USADepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0419, USADepartment of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, MO 66160, USADepartment of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, MO 66160, USACedars-Sinai Medical Center, Los Angeles, CA 90048, USACedars-Sinai Medical Center, Los Angeles, CA 90048, USADepartment of Physiology, Louisiana State University Health Sciences Center-New Orleans, New Orleans, LA 70112, USADepartment of Physiology, Louisiana State University Health Sciences Center-New Orleans, New Orleans, LA 70112, USAProgram Director, Division of Metabolism and Health Effects, National Institute on Alcohol Abuse and Alcoholism, Bethesda, MD 20892-6902, USADepartment of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USADepartment of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USADepartment of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USAChronic 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.https://www.mdpi.com/2218-273X/10/5/669alcoholfatty acid ethyl esterspancreatitisendoplasmic reticulum stressautophagylysosome
collection DOAJ
language English
format Article
sources DOAJ
author Karuna Rasineni
Mukund P. Srinivasan
Appakalai N. Balamurugan
Bhupendra S. Kaphalia
Shaogui Wang
Wen-Xing Ding
Stephen J. Pandol
Aurelia Lugea
Liz Simon
Patricia E. Molina
Peter Gao
Carol A. Casey
Natalia A. Osna
Kusum K. Kharbanda
spellingShingle Karuna Rasineni
Mukund P. Srinivasan
Appakalai N. Balamurugan
Bhupendra S. Kaphalia
Shaogui Wang
Wen-Xing Ding
Stephen J. Pandol
Aurelia Lugea
Liz Simon
Patricia E. Molina
Peter Gao
Carol A. Casey
Natalia A. Osna
Kusum K. Kharbanda
Recent Advances in Understanding the Complexity of Alcohol-Induced Pancreatic Dysfunction and Pancreatitis Development
Biomolecules
alcohol
fatty acid ethyl esters
pancreatitis
endoplasmic reticulum stress
autophagy
lysosome
author_facet Karuna Rasineni
Mukund P. Srinivasan
Appakalai N. Balamurugan
Bhupendra S. Kaphalia
Shaogui Wang
Wen-Xing Ding
Stephen J. Pandol
Aurelia Lugea
Liz Simon
Patricia E. Molina
Peter Gao
Carol A. Casey
Natalia A. Osna
Kusum K. Kharbanda
author_sort Karuna Rasineni
title 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_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_sort recent advances in understanding the complexity of alcohol-induced pancreatic dysfunction and pancreatitis development
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2020-04-01
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.
topic alcohol
fatty acid ethyl esters
pancreatitis
endoplasmic reticulum stress
autophagy
lysosome
url https://www.mdpi.com/2218-273X/10/5/669
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