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High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs
Non-alcoholic fatty liver disease (NAFLD) is an increasingly prevalent condition that has been linked to high-fructose corn syrup consumption with induction of hepatic de novo lipogenesis (DNL) as the suggested central mechanism. Feeding diets very high in fructose (> 60%) rapidly induce several...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854584/ https://www.ncbi.nlm.nih.gov/pubmed/33531575 http://dx.doi.org/10.1038/s41598-021-82208-1 |
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author | Schmidt, Nikolaj H. Svendsen, Pia Albarrán-Juárez, Julián Moestrup, Søren K. Bentzon, Jacob Fog |
author_facet | Schmidt, Nikolaj H. Svendsen, Pia Albarrán-Juárez, Julián Moestrup, Søren K. Bentzon, Jacob Fog |
author_sort | Schmidt, Nikolaj H. |
collection | PubMed |
description | Non-alcoholic fatty liver disease (NAFLD) is an increasingly prevalent condition that has been linked to high-fructose corn syrup consumption with induction of hepatic de novo lipogenesis (DNL) as the suggested central mechanism. Feeding diets very high in fructose (> 60%) rapidly induce several features of NAFLD in rodents, but similar diets have not yet been applied in larger animals, such as pigs. With the aim to develop a large animal NAFLD model, we analysed the effects of feeding a high-fructose (HF, 60% w/w) diet for four weeks to castrated male Danish Landrace-York-Duroc pigs. HF feeding upregulated expression of hepatic DNL proteins, but levels were low compared with adipose tissue. No steatosis or hepatocellular ballooning was seen on histopathological examination, and plasma levels of transaminases were similar between groups. Inflammatory infiltrates and the amount of connective tissue was slightly elevated in liver sections from fructose-fed pigs, which was corroborated by up-regulation of macrophage marker expression in liver homogenates. Supported by RNA-profiling, quantitative protein analysis, histopathological examination, and biochemistry, our data suggest that pigs, contrary to rodents and humans, are protected against fructose-induced steatosis by relying on adipose tissue rather than liver for DNL. |
format | Online Article Text |
id | pubmed-7854584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78545842021-02-03 High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs Schmidt, Nikolaj H. Svendsen, Pia Albarrán-Juárez, Julián Moestrup, Søren K. Bentzon, Jacob Fog Sci Rep Article Non-alcoholic fatty liver disease (NAFLD) is an increasingly prevalent condition that has been linked to high-fructose corn syrup consumption with induction of hepatic de novo lipogenesis (DNL) as the suggested central mechanism. Feeding diets very high in fructose (> 60%) rapidly induce several features of NAFLD in rodents, but similar diets have not yet been applied in larger animals, such as pigs. With the aim to develop a large animal NAFLD model, we analysed the effects of feeding a high-fructose (HF, 60% w/w) diet for four weeks to castrated male Danish Landrace-York-Duroc pigs. HF feeding upregulated expression of hepatic DNL proteins, but levels were low compared with adipose tissue. No steatosis or hepatocellular ballooning was seen on histopathological examination, and plasma levels of transaminases were similar between groups. Inflammatory infiltrates and the amount of connective tissue was slightly elevated in liver sections from fructose-fed pigs, which was corroborated by up-regulation of macrophage marker expression in liver homogenates. Supported by RNA-profiling, quantitative protein analysis, histopathological examination, and biochemistry, our data suggest that pigs, contrary to rodents and humans, are protected against fructose-induced steatosis by relying on adipose tissue rather than liver for DNL. Nature Publishing Group UK 2021-02-02 /pmc/articles/PMC7854584/ /pubmed/33531575 http://dx.doi.org/10.1038/s41598-021-82208-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schmidt, Nikolaj H. Svendsen, Pia Albarrán-Juárez, Julián Moestrup, Søren K. Bentzon, Jacob Fog High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
title | High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
title_full | High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
title_fullStr | High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
title_full_unstemmed | High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
title_short | High-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
title_sort | high-fructose feeding does not induce steatosis or non-alcoholic fatty liver disease in pigs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854584/ https://www.ncbi.nlm.nih.gov/pubmed/33531575 http://dx.doi.org/10.1038/s41598-021-82208-1 |
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