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Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?

Non-alcoholic fatty liver disease (NAFLD) prevalence has increased drastically in recent decades, affecting up to 25% of the world’s population. NAFLD is a spectrum of different diseases that starts with asymptomatic steatosis and continues with development of an inflammatory response called steatoh...

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Autores principales: Martin-Grau, Maria, Marrachelli, Vannina G, Monleon, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891675/
https://www.ncbi.nlm.nih.gov/pubmed/35317178
http://dx.doi.org/10.4254/wjh.v14.i2.304
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author Martin-Grau, Maria
Marrachelli, Vannina G
Monleon, Daniel
author_facet Martin-Grau, Maria
Marrachelli, Vannina G
Monleon, Daniel
author_sort Martin-Grau, Maria
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) prevalence has increased drastically in recent decades, affecting up to 25% of the world’s population. NAFLD is a spectrum of different diseases that starts with asymptomatic steatosis and continues with development of an inflammatory response called steatohepatitis, which can progress to fibrosis. Several molecular and metabolic changes are required for the hepatocyte to finally vary its function; hence a “multiple hit” hypothesis seems a more accurate proposal. Previous studies and current knowledge suggest that in most cases, NAFLD initiates and progresses through most of nine hallmarks of the disease, although the triggers and mechanisms for these can vary widely. The use of animal models remains crucial for understanding the disease and for developing tools based on biological knowledge. Among certain requirements to be met, a good model must imitate certain aspects of the human NAFLD disorder, be reliable and reproducible, have low mortality, and be compatible with a simple and feasible method. Metabolism studies in these models provides a direct reflection of the workings of the cell and may be a useful approach to better understand the initiation and progression of the disease. Metabolomics seems a valid tool for studying metabolic pathways and crosstalk between organs affected in animal models of NAFLD and for the discovery and validation of relevant biomarkers with biological understanding. In this review, we provide a brief introduction to NAFLD hallmarks, the five groups of animal models available for studying NAFLD and the potential role of metabolomics in the study of experimental NAFLD.
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spelling pubmed-88916752022-03-21 Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn? Martin-Grau, Maria Marrachelli, Vannina G Monleon, Daniel World J Hepatol Review Non-alcoholic fatty liver disease (NAFLD) prevalence has increased drastically in recent decades, affecting up to 25% of the world’s population. NAFLD is a spectrum of different diseases that starts with asymptomatic steatosis and continues with development of an inflammatory response called steatohepatitis, which can progress to fibrosis. Several molecular and metabolic changes are required for the hepatocyte to finally vary its function; hence a “multiple hit” hypothesis seems a more accurate proposal. Previous studies and current knowledge suggest that in most cases, NAFLD initiates and progresses through most of nine hallmarks of the disease, although the triggers and mechanisms for these can vary widely. The use of animal models remains crucial for understanding the disease and for developing tools based on biological knowledge. Among certain requirements to be met, a good model must imitate certain aspects of the human NAFLD disorder, be reliable and reproducible, have low mortality, and be compatible with a simple and feasible method. Metabolism studies in these models provides a direct reflection of the workings of the cell and may be a useful approach to better understand the initiation and progression of the disease. Metabolomics seems a valid tool for studying metabolic pathways and crosstalk between organs affected in animal models of NAFLD and for the discovery and validation of relevant biomarkers with biological understanding. In this review, we provide a brief introduction to NAFLD hallmarks, the five groups of animal models available for studying NAFLD and the potential role of metabolomics in the study of experimental NAFLD. Baishideng Publishing Group Inc 2022-02-27 2022-02-27 /pmc/articles/PMC8891675/ /pubmed/35317178 http://dx.doi.org/10.4254/wjh.v14.i2.304 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Review
Martin-Grau, Maria
Marrachelli, Vannina G
Monleon, Daniel
Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?
title Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?
title_full Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?
title_fullStr Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?
title_full_unstemmed Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?
title_short Rodent models and metabolomics in non-alcoholic fatty liver disease: What can we learn?
title_sort rodent models and metabolomics in non-alcoholic fatty liver disease: what can we learn?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891675/
https://www.ncbi.nlm.nih.gov/pubmed/35317178
http://dx.doi.org/10.4254/wjh.v14.i2.304
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