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Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis
Dietary arginine (Arg) supplementation has been proposed to have positive effects on the development of liver diseases. In the present study, we investigate if an oral Arg supplementation in diet protects mice fed a fructose, fat and cholesterol enriched Western-style diet (WSD) from the development...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487836/ https://www.ncbi.nlm.nih.gov/pubmed/28434046 http://dx.doi.org/10.1007/s00726-017-2423-4 |
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author | Sellmann, Cathrin Degen, Christian Jin, Cheng Jun Nier, Anika Engstler, Anna Janina Hasan Alkhatib, Dana De Bandt, Jean-Pascal Bergheim, Ina |
author_facet | Sellmann, Cathrin Degen, Christian Jin, Cheng Jun Nier, Anika Engstler, Anna Janina Hasan Alkhatib, Dana De Bandt, Jean-Pascal Bergheim, Ina |
author_sort | Sellmann, Cathrin |
collection | PubMed |
description | Dietary arginine (Arg) supplementation has been proposed to have positive effects on the development of liver diseases. In the present study, we investigate if an oral Arg supplementation in diet protects mice fed a fructose, fat and cholesterol enriched Western-style diet (WSD) from the development of non-alcoholic steatohepatitis (NASH). Female C57BL/6J mice were fed a liquid control diet or a liquid WSD ± Arg (2.49 g/kg body weight/day) for 6 weeks. Indices of liver injury, glucose metabolism and intestinal permeability were determined. While Arg supplementation had no effects on body weight gain, fasting blood glucose levels were significantly lower in WSD+Arg-fed mice than in C+Arg-fed animals. WSD-fed mice developed liver steatosis accompanied with inflammation, both being significantly attenuated in WSD+Arg-fed mice. These effects of Arg supplementation went along with a protection against WSD-induced decreased tight junction protein levels in the upper parts of the small intestine, increased levels of bacterial endotoxin in portal plasma as well as increased hepatic toll-like receptor-4 mRNA and 4-hydroxynonenal protein adduct levels. In conclusion, Arg supplementation may protect mice from the development of NASH. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00726-017-2423-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5487836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-54878362017-07-03 Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis Sellmann, Cathrin Degen, Christian Jin, Cheng Jun Nier, Anika Engstler, Anna Janina Hasan Alkhatib, Dana De Bandt, Jean-Pascal Bergheim, Ina Amino Acids Original Article Dietary arginine (Arg) supplementation has been proposed to have positive effects on the development of liver diseases. In the present study, we investigate if an oral Arg supplementation in diet protects mice fed a fructose, fat and cholesterol enriched Western-style diet (WSD) from the development of non-alcoholic steatohepatitis (NASH). Female C57BL/6J mice were fed a liquid control diet or a liquid WSD ± Arg (2.49 g/kg body weight/day) for 6 weeks. Indices of liver injury, glucose metabolism and intestinal permeability were determined. While Arg supplementation had no effects on body weight gain, fasting blood glucose levels were significantly lower in WSD+Arg-fed mice than in C+Arg-fed animals. WSD-fed mice developed liver steatosis accompanied with inflammation, both being significantly attenuated in WSD+Arg-fed mice. These effects of Arg supplementation went along with a protection against WSD-induced decreased tight junction protein levels in the upper parts of the small intestine, increased levels of bacterial endotoxin in portal plasma as well as increased hepatic toll-like receptor-4 mRNA and 4-hydroxynonenal protein adduct levels. In conclusion, Arg supplementation may protect mice from the development of NASH. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00726-017-2423-4) contains supplementary material, which is available to authorized users. Springer Vienna 2017-04-22 2017 /pmc/articles/PMC5487836/ /pubmed/28434046 http://dx.doi.org/10.1007/s00726-017-2423-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Sellmann, Cathrin Degen, Christian Jin, Cheng Jun Nier, Anika Engstler, Anna Janina Hasan Alkhatib, Dana De Bandt, Jean-Pascal Bergheim, Ina Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
title | Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
title_full | Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
title_fullStr | Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
title_full_unstemmed | Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
title_short | Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
title_sort | oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487836/ https://www.ncbi.nlm.nih.gov/pubmed/28434046 http://dx.doi.org/10.1007/s00726-017-2423-4 |
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