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Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study

Obesity, ethanol, and contaminants are known risk factors of cardiovascular and metabolic diseases (CMD). However, their interplay on clinical profiles of these diseases remains unclear, and thus were investigated in this study. Male lean or obese JCR rats were given water or 10% ethanol and orally...

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Autores principales: Florian, Maria, Li, Bai, Patry, Dominique, Truong, Jocelyn, Caldwell, Don, Coughlan, Melanie C., Woodworth, Robert, Yan, Jin, Chen, Qixuan, Petrov, Ivan, Mahemuti, Laziyan, Lalande, Michelle, Li, Nanqin, Chan, Laurie H. M., Willmore, William G., Jin, Xiaolei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107407/
https://www.ncbi.nlm.nih.gov/pubmed/35429258
http://dx.doi.org/10.1007/s12012-022-09738-6
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author Florian, Maria
Li, Bai
Patry, Dominique
Truong, Jocelyn
Caldwell, Don
Coughlan, Melanie C.
Woodworth, Robert
Yan, Jin
Chen, Qixuan
Petrov, Ivan
Mahemuti, Laziyan
Lalande, Michelle
Li, Nanqin
Chan, Laurie H. M.
Willmore, William G.
Jin, Xiaolei
author_facet Florian, Maria
Li, Bai
Patry, Dominique
Truong, Jocelyn
Caldwell, Don
Coughlan, Melanie C.
Woodworth, Robert
Yan, Jin
Chen, Qixuan
Petrov, Ivan
Mahemuti, Laziyan
Lalande, Michelle
Li, Nanqin
Chan, Laurie H. M.
Willmore, William G.
Jin, Xiaolei
author_sort Florian, Maria
collection PubMed
description Obesity, ethanol, and contaminants are known risk factors of cardiovascular and metabolic diseases (CMD). However, their interplay on clinical profiles of these diseases remains unclear, and thus were investigated in this study. Male lean or obese JCR rats were given water or 10% ethanol and orally treated with or without a contaminant mixture (CM) dissolved in corn oil and loaded on two cookies at 0, 1.6, or 16 mg/kg BW/day dose levels for 4 weeks. The CM consisted 22 environmental contaminants found in human blood or serum of Northern populations. Over 60 parameters related to CMD were examined. The results revealed that obesity in JCR rats resembles the clinical profiles of non-alcoholic fatty liver disease in humans. Obesity was also associated with increased serum and organ retention of mercury, one of the chemical components of CM. Exposure to ethanol lightened hyperlipidemia, increased liver retention of mercury, and increased risk for hypertension in the obese rats. CM lessened hyperlipidemia and hyperenzymemia, worsened systemic inflammation and increased the risk for hypertension in the obese rats. CM markedly increased serum ethanol levels with or without ethanol exposure. Tissue total mercury contents significantly correlated with clinical parameters with altered profiles by both ethanol and obesity. These results suggest that obese individuals may be more prone to contaminant accumulation. Ethanol and CM exposure can alter clinical profiles associated with obesity, which may lead to misdiagnosis of CMD associated with obesity. CM can alter endogenous production and/or metabolism of ethanol, further complicating disease progression, diagnosis, and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12012-022-09738-6.
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spelling pubmed-91074072022-05-16 Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study Florian, Maria Li, Bai Patry, Dominique Truong, Jocelyn Caldwell, Don Coughlan, Melanie C. Woodworth, Robert Yan, Jin Chen, Qixuan Petrov, Ivan Mahemuti, Laziyan Lalande, Michelle Li, Nanqin Chan, Laurie H. M. Willmore, William G. Jin, Xiaolei Cardiovasc Toxicol Article Obesity, ethanol, and contaminants are known risk factors of cardiovascular and metabolic diseases (CMD). However, their interplay on clinical profiles of these diseases remains unclear, and thus were investigated in this study. Male lean or obese JCR rats were given water or 10% ethanol and orally treated with or without a contaminant mixture (CM) dissolved in corn oil and loaded on two cookies at 0, 1.6, or 16 mg/kg BW/day dose levels for 4 weeks. The CM consisted 22 environmental contaminants found in human blood or serum of Northern populations. Over 60 parameters related to CMD were examined. The results revealed that obesity in JCR rats resembles the clinical profiles of non-alcoholic fatty liver disease in humans. Obesity was also associated with increased serum and organ retention of mercury, one of the chemical components of CM. Exposure to ethanol lightened hyperlipidemia, increased liver retention of mercury, and increased risk for hypertension in the obese rats. CM lessened hyperlipidemia and hyperenzymemia, worsened systemic inflammation and increased the risk for hypertension in the obese rats. CM markedly increased serum ethanol levels with or without ethanol exposure. Tissue total mercury contents significantly correlated with clinical parameters with altered profiles by both ethanol and obesity. These results suggest that obese individuals may be more prone to contaminant accumulation. Ethanol and CM exposure can alter clinical profiles associated with obesity, which may lead to misdiagnosis of CMD associated with obesity. CM can alter endogenous production and/or metabolism of ethanol, further complicating disease progression, diagnosis, and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12012-022-09738-6. Springer US 2022-04-16 2022 /pmc/articles/PMC9107407/ /pubmed/35429258 http://dx.doi.org/10.1007/s12012-022-09738-6 Text en © Crown 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Florian, Maria
Li, Bai
Patry, Dominique
Truong, Jocelyn
Caldwell, Don
Coughlan, Melanie C.
Woodworth, Robert
Yan, Jin
Chen, Qixuan
Petrov, Ivan
Mahemuti, Laziyan
Lalande, Michelle
Li, Nanqin
Chan, Laurie H. M.
Willmore, William G.
Jin, Xiaolei
Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study
title Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study
title_full Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study
title_fullStr Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study
title_full_unstemmed Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study
title_short Interplay of Obesity, Ethanol, and Contaminant Mixture on Clinical Profiles of Cardiovascular and Metabolic Diseases: Evidence from an Animal Study
title_sort interplay of obesity, ethanol, and contaminant mixture on clinical profiles of cardiovascular and metabolic diseases: evidence from an animal study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107407/
https://www.ncbi.nlm.nih.gov/pubmed/35429258
http://dx.doi.org/10.1007/s12012-022-09738-6
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