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Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice

AGEs are a heterogeneous group of molecules formed from the nonenzymatic reaction of reducing sugars with free amino groups of proteins, lipids, and/or nucleic acids. AGEs have been shown to play a role in various conditions including cardiovascular disease and diabetes. In this study, we hypothesiz...

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Autores principales: Sayej, Wael N., Knight III, Paul R., Guo, Weidun Alan, Mullan, Barbara, Ohtake, Patricia J., Davidson, Bruce A., Khan, Abdur, Baker, Robert D., Baker, Susan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753052/
https://www.ncbi.nlm.nih.gov/pubmed/26942201
http://dx.doi.org/10.1155/2016/7867852
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author Sayej, Wael N.
Knight III, Paul R.
Guo, Weidun Alan
Mullan, Barbara
Ohtake, Patricia J.
Davidson, Bruce A.
Khan, Abdur
Baker, Robert D.
Baker, Susan S.
author_facet Sayej, Wael N.
Knight III, Paul R.
Guo, Weidun Alan
Mullan, Barbara
Ohtake, Patricia J.
Davidson, Bruce A.
Khan, Abdur
Baker, Robert D.
Baker, Susan S.
author_sort Sayej, Wael N.
collection PubMed
description AGEs are a heterogeneous group of molecules formed from the nonenzymatic reaction of reducing sugars with free amino groups of proteins, lipids, and/or nucleic acids. AGEs have been shown to play a role in various conditions including cardiovascular disease and diabetes. In this study, we hypothesized that AGEs play a role in the “multiple hit hypothesis” of nonalcoholic fatty liver disease (NAFLD) and contribute to the pathogenesis of hepatosteatosis. We measured the effects of various mouse chows containing high or low AGE in the presence of high or low fat content on mouse weight and epididymal fat pads. We also measured the effects of these chows on the inflammatory response by measuring cytokine levels and myeloperoxidase activity levels on liver supernatants. We observed significant differences in weight gain and epididymal fat pad weights in the high AGE-high fat (HAGE-HF) versus the other groups. Leptin, TNF-α, IL-6, and myeloperoxidase (MPO) levels were significantly higher in the HAGE-HF group. We conclude that a diet containing high AGEs in the presence of high fat induces weight gain and hepatosteatosis in CD-1 mice. This may represent a model to study the role of AGEs in the pathogenesis of hepatosteatosis and steatohepatitis.
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spelling pubmed-47530522016-03-03 Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice Sayej, Wael N. Knight III, Paul R. Guo, Weidun Alan Mullan, Barbara Ohtake, Patricia J. Davidson, Bruce A. Khan, Abdur Baker, Robert D. Baker, Susan S. Biomed Res Int Research Article AGEs are a heterogeneous group of molecules formed from the nonenzymatic reaction of reducing sugars with free amino groups of proteins, lipids, and/or nucleic acids. AGEs have been shown to play a role in various conditions including cardiovascular disease and diabetes. In this study, we hypothesized that AGEs play a role in the “multiple hit hypothesis” of nonalcoholic fatty liver disease (NAFLD) and contribute to the pathogenesis of hepatosteatosis. We measured the effects of various mouse chows containing high or low AGE in the presence of high or low fat content on mouse weight and epididymal fat pads. We also measured the effects of these chows on the inflammatory response by measuring cytokine levels and myeloperoxidase activity levels on liver supernatants. We observed significant differences in weight gain and epididymal fat pad weights in the high AGE-high fat (HAGE-HF) versus the other groups. Leptin, TNF-α, IL-6, and myeloperoxidase (MPO) levels were significantly higher in the HAGE-HF group. We conclude that a diet containing high AGEs in the presence of high fat induces weight gain and hepatosteatosis in CD-1 mice. This may represent a model to study the role of AGEs in the pathogenesis of hepatosteatosis and steatohepatitis. Hindawi Publishing Corporation 2016 2016-01-31 /pmc/articles/PMC4753052/ /pubmed/26942201 http://dx.doi.org/10.1155/2016/7867852 Text en Copyright © 2016 Wael N. Sayej et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sayej, Wael N.
Knight III, Paul R.
Guo, Weidun Alan
Mullan, Barbara
Ohtake, Patricia J.
Davidson, Bruce A.
Khan, Abdur
Baker, Robert D.
Baker, Susan S.
Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice
title Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice
title_full Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice
title_fullStr Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice
title_full_unstemmed Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice
title_short Advanced Glycation End Products Induce Obesity and Hepatosteatosis in CD-1 Wild-Type Mice
title_sort advanced glycation end products induce obesity and hepatosteatosis in cd-1 wild-type mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753052/
https://www.ncbi.nlm.nih.gov/pubmed/26942201
http://dx.doi.org/10.1155/2016/7867852
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