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Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate

The administration of monosodium glutamate (MSG) to mice induces hepatic steatosis and inflammation. In this study, we investigated the metabolic features of MSG-treated mice and the histological changes that occur in their livers and adipose tissue. MSG mice were prepared by subcutaneously injectin...

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Autores principales: Takai, Atsuko, Kikuchi, Kentaro, Kajiyama, Yusuke, Sugiura, Anna, Negishi, Masatsugu, Tsunashima, Hiromichi, Yamada, Hanae, Matsumoto, Kotaro, Tsuneyama, Koichi, Moritoki, Yuki, Hara, Masumi, Miyakawa, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897218/
https://www.ncbi.nlm.nih.gov/pubmed/27433515
http://dx.doi.org/10.1155/2014/725351
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author Takai, Atsuko
Kikuchi, Kentaro
Kajiyama, Yusuke
Sugiura, Anna
Negishi, Masatsugu
Tsunashima, Hiromichi
Yamada, Hanae
Matsumoto, Kotaro
Tsuneyama, Koichi
Moritoki, Yuki
Hara, Masumi
Miyakawa, Hiroshi
author_facet Takai, Atsuko
Kikuchi, Kentaro
Kajiyama, Yusuke
Sugiura, Anna
Negishi, Masatsugu
Tsunashima, Hiromichi
Yamada, Hanae
Matsumoto, Kotaro
Tsuneyama, Koichi
Moritoki, Yuki
Hara, Masumi
Miyakawa, Hiroshi
author_sort Takai, Atsuko
collection PubMed
description The administration of monosodium glutamate (MSG) to mice induces hepatic steatosis and inflammation. In this study, we investigated the metabolic features of MSG-treated mice and the histological changes that occur in their livers and adipose tissue. MSG mice were prepared by subcutaneously injecting MSG into newborn C57BL/6J male mice. The control mice were subcutaneously injected with saline. Another group of mice was fed a methionine- and choline-deficient diet (MCD). Compared with the control mice, the MSG mice had higher serum levels of insulin and cholesterol than the control mice, whereas the opposite was true for the MCD mice. Microvesicular steatosis and inflammatory cell infiltration were detected in both the MSG and MCD mouse livers. Enlarged adipocytes and crown-like structures were observed in the epididymal fat of the MSG mice, whereas neither of these features was seen in the MCD mice. Flow cytometric analysis revealed increased frequencies of monocytes and M1 macrophages in the livers and epididymal fat tissue of the MSG mice, respectively. The MSG mice exhibited the characteristic liver histopathology of nonalcoholic steatohepatitis (NASH) as well as metabolic syndrome-like features, which suggested that MSG mice are a better model of human NASH than MCD mice.
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spelling pubmed-48972182016-07-18 Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate Takai, Atsuko Kikuchi, Kentaro Kajiyama, Yusuke Sugiura, Anna Negishi, Masatsugu Tsunashima, Hiromichi Yamada, Hanae Matsumoto, Kotaro Tsuneyama, Koichi Moritoki, Yuki Hara, Masumi Miyakawa, Hiroshi Int Sch Res Notices Research Article The administration of monosodium glutamate (MSG) to mice induces hepatic steatosis and inflammation. In this study, we investigated the metabolic features of MSG-treated mice and the histological changes that occur in their livers and adipose tissue. MSG mice were prepared by subcutaneously injecting MSG into newborn C57BL/6J male mice. The control mice were subcutaneously injected with saline. Another group of mice was fed a methionine- and choline-deficient diet (MCD). Compared with the control mice, the MSG mice had higher serum levels of insulin and cholesterol than the control mice, whereas the opposite was true for the MCD mice. Microvesicular steatosis and inflammatory cell infiltration were detected in both the MSG and MCD mouse livers. Enlarged adipocytes and crown-like structures were observed in the epididymal fat of the MSG mice, whereas neither of these features was seen in the MCD mice. Flow cytometric analysis revealed increased frequencies of monocytes and M1 macrophages in the livers and epididymal fat tissue of the MSG mice, respectively. The MSG mice exhibited the characteristic liver histopathology of nonalcoholic steatohepatitis (NASH) as well as metabolic syndrome-like features, which suggested that MSG mice are a better model of human NASH than MCD mice. Hindawi Publishing Corporation 2014-10-30 /pmc/articles/PMC4897218/ /pubmed/27433515 http://dx.doi.org/10.1155/2014/725351 Text en Copyright © 2014 Atsuko Takai et al. https://creativecommons.org/licenses/by/3.0/ 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
Takai, Atsuko
Kikuchi, Kentaro
Kajiyama, Yusuke
Sugiura, Anna
Negishi, Masatsugu
Tsunashima, Hiromichi
Yamada, Hanae
Matsumoto, Kotaro
Tsuneyama, Koichi
Moritoki, Yuki
Hara, Masumi
Miyakawa, Hiroshi
Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate
title Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate
title_full Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate
title_fullStr Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate
title_full_unstemmed Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate
title_short Serological and Histological Examination of a Nonalcoholic Steatohepatitis Mouse Model Created via the Administration of Monosodium Glutamate
title_sort serological and histological examination of a nonalcoholic steatohepatitis mouse model created via the administration of monosodium glutamate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897218/
https://www.ncbi.nlm.nih.gov/pubmed/27433515
http://dx.doi.org/10.1155/2014/725351
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