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Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats
We set out to explore the hypothesis that glycine attenuates non-alcoholic steatohepatitis (NASH) in rats and the possible mechanism by which is it does. Male Sprague-Dawley (SD) rats were fed a diet containing high fat and high sucrose (HSHF) for 24 weeks to induce NASH. Blood and liver tissues wer...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348315/ https://www.ncbi.nlm.nih.gov/pubmed/27784003 http://dx.doi.org/10.18632/oncotarget.12831 |
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author | Zhou, Xin Han, Dewu Xu, Ruiling Wu, Huiwen Qu, Chongxiao Wang, Feng Wang, Xiangyu Zhao, Yuanchang |
author_facet | Zhou, Xin Han, Dewu Xu, Ruiling Wu, Huiwen Qu, Chongxiao Wang, Feng Wang, Xiangyu Zhao, Yuanchang |
author_sort | Zhou, Xin |
collection | PubMed |
description | We set out to explore the hypothesis that glycine attenuates non-alcoholic steatohepatitis (NASH) in rats and the possible mechanism by which is it does. Male Sprague-Dawley (SD) rats were fed a diet containing high fat and high sucrose (HSHF) for 24 weeks to induce NASH. Blood and liver tissues were sampled at selected time points throughout the study. Compared with control animals, the content of alanine transaminase (ALT), triglycerides (TGs), and free fatty acids (FFAs) in plasma and the TG and FFA content in the liver was increased from week 4 to 24. The level of TNF(α) and MCP-1 in plasma, the content of TNF(α) in the liver, the insulin resistance index, inflammatory cell infiltration, hepatocyte apoptosis, reactive oxygen species (ROS) generation, and endoplasmic stress-associated protein expression were unaltered at 4 weeks. However, these levels were significantly elevated in HSHF fed rats at 12 weeks. At the same time, the level of endotoxin progressively increased from 0.08 ± 0.02 endotoxin EU/ml at week 4 to 0.7 ± 0.19 EU/ml at week 24. Moreover, these rats had elevated blood endotoxin levels, which were positively associated with their NASH indexes. Liver histology progressively worsened over the course of the study. However, we found that with concomitant treatment with glycine, the level of endotoxin decreased, while NASH indexes significantly decreased and liver status markedly improved,. These data support the hypothesis that glycine protects against NASH in rats by decreasing the levels of intestinal endotoxin, alleviating endoplasmic reticulum and oxidative stress. |
format | Online Article Text |
id | pubmed-5348315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53483152017-03-31 Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats Zhou, Xin Han, Dewu Xu, Ruiling Wu, Huiwen Qu, Chongxiao Wang, Feng Wang, Xiangyu Zhao, Yuanchang Oncotarget Research Paper: Pathology We set out to explore the hypothesis that glycine attenuates non-alcoholic steatohepatitis (NASH) in rats and the possible mechanism by which is it does. Male Sprague-Dawley (SD) rats were fed a diet containing high fat and high sucrose (HSHF) for 24 weeks to induce NASH. Blood and liver tissues were sampled at selected time points throughout the study. Compared with control animals, the content of alanine transaminase (ALT), triglycerides (TGs), and free fatty acids (FFAs) in plasma and the TG and FFA content in the liver was increased from week 4 to 24. The level of TNF(α) and MCP-1 in plasma, the content of TNF(α) in the liver, the insulin resistance index, inflammatory cell infiltration, hepatocyte apoptosis, reactive oxygen species (ROS) generation, and endoplasmic stress-associated protein expression were unaltered at 4 weeks. However, these levels were significantly elevated in HSHF fed rats at 12 weeks. At the same time, the level of endotoxin progressively increased from 0.08 ± 0.02 endotoxin EU/ml at week 4 to 0.7 ± 0.19 EU/ml at week 24. Moreover, these rats had elevated blood endotoxin levels, which were positively associated with their NASH indexes. Liver histology progressively worsened over the course of the study. However, we found that with concomitant treatment with glycine, the level of endotoxin decreased, while NASH indexes significantly decreased and liver status markedly improved,. These data support the hypothesis that glycine protects against NASH in rats by decreasing the levels of intestinal endotoxin, alleviating endoplasmic reticulum and oxidative stress. Impact Journals LLC 2016-10-23 /pmc/articles/PMC5348315/ /pubmed/27784003 http://dx.doi.org/10.18632/oncotarget.12831 Text en Copyright: © 2016 Zhou et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Pathology Zhou, Xin Han, Dewu Xu, Ruiling Wu, Huiwen Qu, Chongxiao Wang, Feng Wang, Xiangyu Zhao, Yuanchang Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
title | Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
title_full | Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
title_fullStr | Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
title_full_unstemmed | Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
title_short | Glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
title_sort | glycine protects against high sucrose and high fat-induced non-alcoholic steatohepatitis in rats |
topic | Research Paper: Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348315/ https://www.ncbi.nlm.nih.gov/pubmed/27784003 http://dx.doi.org/10.18632/oncotarget.12831 |
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