Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1782415825812062208 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4753052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sayejwaeln advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT knightiiipaulr advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT guoweidunalan advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT mullanbarbara advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT ohtakepatriciaj advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT davidsonbrucea advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT khanabdur advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT bakerrobertd advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice AT bakersusans advancedglycationendproductsinduceobesityandhepatosteatosisincd1wildtypemice |