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Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice
Nonalcoholic fatty liver disease (NAFLD) in non-obese patients remains a clinical condition with unclear etiology and pathogenesis. Using a metabolomics approach in a mouse model that recapitulates almost all the characteristic features of non-obese NAFLD, we aimed to advance mechanistic understandi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522413/ https://www.ncbi.nlm.nih.gov/pubmed/28733574 http://dx.doi.org/10.1038/s41598-017-05040-6 |
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author | Tu, Lan N. Showalter, Megan R. Cajka, Tomas Fan, Sili Pillai, Viju V. Fiehn, Oliver Selvaraj, Vimal |
author_facet | Tu, Lan N. Showalter, Megan R. Cajka, Tomas Fan, Sili Pillai, Viju V. Fiehn, Oliver Selvaraj, Vimal |
author_sort | Tu, Lan N. |
collection | PubMed |
description | Nonalcoholic fatty liver disease (NAFLD) in non-obese patients remains a clinical condition with unclear etiology and pathogenesis. Using a metabolomics approach in a mouse model that recapitulates almost all the characteristic features of non-obese NAFLD, we aimed to advance mechanistic understanding of this disorder. Mice fed high fat, high cholesterol, cholate (HFHCC) diet for three weeks consistently developed hepatic pathology similar to NAFLD and nonalcoholic steatohepatitis (NASH) without changes to body weight or fat pad weights. Gas- and liquid chromatography/mass spectrometry-based profiling of lipidomic and primary metabolism changes in the liver and plasma revealed that systemic mechanisms leading to steatosis and hepatitis in this non-obese NAFLD model were driven by a combination of effects directed by elevated free cholesterol, cholesterol esters and cholic acid, and associated changes to metabolism of sphingomyelins and phosphatidylcholines. These results demonstrate that mechanisms underlying cholesterol-induced non-obese NAFLD are distinct from NAFLD occurring as a consequence of metabolic syndrome. In addition, this investigation provides one of the first metabolite reference profiles for interpreting effects of dietary and hepatic cholesterol in human non-obese NAFLD/NASH patients. |
format | Online Article Text |
id | pubmed-5522413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55224132017-07-26 Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice Tu, Lan N. Showalter, Megan R. Cajka, Tomas Fan, Sili Pillai, Viju V. Fiehn, Oliver Selvaraj, Vimal Sci Rep Article Nonalcoholic fatty liver disease (NAFLD) in non-obese patients remains a clinical condition with unclear etiology and pathogenesis. Using a metabolomics approach in a mouse model that recapitulates almost all the characteristic features of non-obese NAFLD, we aimed to advance mechanistic understanding of this disorder. Mice fed high fat, high cholesterol, cholate (HFHCC) diet for three weeks consistently developed hepatic pathology similar to NAFLD and nonalcoholic steatohepatitis (NASH) without changes to body weight or fat pad weights. Gas- and liquid chromatography/mass spectrometry-based profiling of lipidomic and primary metabolism changes in the liver and plasma revealed that systemic mechanisms leading to steatosis and hepatitis in this non-obese NAFLD model were driven by a combination of effects directed by elevated free cholesterol, cholesterol esters and cholic acid, and associated changes to metabolism of sphingomyelins and phosphatidylcholines. These results demonstrate that mechanisms underlying cholesterol-induced non-obese NAFLD are distinct from NAFLD occurring as a consequence of metabolic syndrome. In addition, this investigation provides one of the first metabolite reference profiles for interpreting effects of dietary and hepatic cholesterol in human non-obese NAFLD/NASH patients. Nature Publishing Group UK 2017-07-21 /pmc/articles/PMC5522413/ /pubmed/28733574 http://dx.doi.org/10.1038/s41598-017-05040-6 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tu, Lan N. Showalter, Megan R. Cajka, Tomas Fan, Sili Pillai, Viju V. Fiehn, Oliver Selvaraj, Vimal Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
title | Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
title_full | Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
title_fullStr | Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
title_full_unstemmed | Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
title_short | Metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
title_sort | metabolomic characteristics of cholesterol-induced non-obese nonalcoholic fatty liver disease in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522413/ https://www.ncbi.nlm.nih.gov/pubmed/28733574 http://dx.doi.org/10.1038/s41598-017-05040-6 |
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