Cargando…

Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis

Research in nonalcoholic fatty liver disease (NAFLD), including nonalcoholic steatohepatitis (NASH), has been limited by the availability of suitable models for this disease. A number of rodent models have been described in which the relevant liver pathology develops in an appropriate metabolic cont...

Descripción completa

Detalles Bibliográficos
Autores principales: Imajo, Kento, Yoneda, Masato, Kessoku, Takaomi, Ogawa, Yuji, Maeda, Shin, Sumida, Yoshio, Hyogo, Hideyuki, Eguchi, Yuichiro, Wada, Koichiro, Nakajima, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856038/
https://www.ncbi.nlm.nih.gov/pubmed/24192824
http://dx.doi.org/10.3390/ijms141121833
_version_ 1782295005322280960
author Imajo, Kento
Yoneda, Masato
Kessoku, Takaomi
Ogawa, Yuji
Maeda, Shin
Sumida, Yoshio
Hyogo, Hideyuki
Eguchi, Yuichiro
Wada, Koichiro
Nakajima, Atsushi
author_facet Imajo, Kento
Yoneda, Masato
Kessoku, Takaomi
Ogawa, Yuji
Maeda, Shin
Sumida, Yoshio
Hyogo, Hideyuki
Eguchi, Yuichiro
Wada, Koichiro
Nakajima, Atsushi
author_sort Imajo, Kento
collection PubMed
description Research in nonalcoholic fatty liver disease (NAFLD), including nonalcoholic steatohepatitis (NASH), has been limited by the availability of suitable models for this disease. A number of rodent models have been described in which the relevant liver pathology develops in an appropriate metabolic context. These models are promising tools for researchers investigating one of the key issues of NASH: not so much why steatosis occurs, but what causes the transition from simple steatosis to the inflammatory, progressive fibrosing condition of steatohepatitis. The different rodent models can be classified into two large groups. The first includes models in which the disease is acquired after dietary or pharmacological manipulation, and the second, genetically modified models in which liver disease develops spontaneously. To date, no single rodent model has encompassed the full spectrum of human disease progression, but individual models can imitate particular characteristics of human disease. Therefore, it is important that researchers choose the appropriate rodent models. The purpose of the present review is to discuss the metabolic abnormalities present in the currently available rodent models of NAFLD, summarizing the strengths and weaknesses of the established models and the key findings that have furthered our understanding of the disease’s pathogenesis.
format Online
Article
Text
id pubmed-3856038
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Molecular Diversity Preservation International (MDPI)
record_format MEDLINE/PubMed
spelling pubmed-38560382013-12-09 Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis Imajo, Kento Yoneda, Masato Kessoku, Takaomi Ogawa, Yuji Maeda, Shin Sumida, Yoshio Hyogo, Hideyuki Eguchi, Yuichiro Wada, Koichiro Nakajima, Atsushi Int J Mol Sci Review Research in nonalcoholic fatty liver disease (NAFLD), including nonalcoholic steatohepatitis (NASH), has been limited by the availability of suitable models for this disease. A number of rodent models have been described in which the relevant liver pathology develops in an appropriate metabolic context. These models are promising tools for researchers investigating one of the key issues of NASH: not so much why steatosis occurs, but what causes the transition from simple steatosis to the inflammatory, progressive fibrosing condition of steatohepatitis. The different rodent models can be classified into two large groups. The first includes models in which the disease is acquired after dietary or pharmacological manipulation, and the second, genetically modified models in which liver disease develops spontaneously. To date, no single rodent model has encompassed the full spectrum of human disease progression, but individual models can imitate particular characteristics of human disease. Therefore, it is important that researchers choose the appropriate rodent models. The purpose of the present review is to discuss the metabolic abnormalities present in the currently available rodent models of NAFLD, summarizing the strengths and weaknesses of the established models and the key findings that have furthered our understanding of the disease’s pathogenesis. Molecular Diversity Preservation International (MDPI) 2013-11-04 /pmc/articles/PMC3856038/ /pubmed/24192824 http://dx.doi.org/10.3390/ijms141121833 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Imajo, Kento
Yoneda, Masato
Kessoku, Takaomi
Ogawa, Yuji
Maeda, Shin
Sumida, Yoshio
Hyogo, Hideyuki
Eguchi, Yuichiro
Wada, Koichiro
Nakajima, Atsushi
Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis
title Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis
title_full Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis
title_fullStr Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis
title_full_unstemmed Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis
title_short Rodent Models of Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis
title_sort rodent models of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856038/
https://www.ncbi.nlm.nih.gov/pubmed/24192824
http://dx.doi.org/10.3390/ijms141121833
work_keys_str_mv AT imajokento rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT yonedamasato rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT kessokutakaomi rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT ogawayuji rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT maedashin rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT sumidayoshio rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT hyogohideyuki rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT eguchiyuichiro rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT wadakoichiro rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis
AT nakajimaatsushi rodentmodelsofnonalcoholicfattyliverdiseasenonalcoholicsteatohepatitis