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The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs

Variability in disease development due to differences in strains and breeders constitutes a substantial challenge in preclinical research. However, the impact of the breeder on non-alcoholic steatohepatitis (NASH) is not yet fully elucidated. This retrospective study investigates NASH development in...

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Autores principales: Ipsen, D. H., Agerskov, R. H., Klaebel, J. H., Lykkesfeldt, J., Tveden-Nyborg, Pernille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859397/
https://www.ncbi.nlm.nih.gov/pubmed/33536590
http://dx.doi.org/10.1038/s41598-021-82643-0
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author Ipsen, D. H.
Agerskov, R. H.
Klaebel, J. H.
Lykkesfeldt, J.
Tveden-Nyborg, Pernille
author_facet Ipsen, D. H.
Agerskov, R. H.
Klaebel, J. H.
Lykkesfeldt, J.
Tveden-Nyborg, Pernille
author_sort Ipsen, D. H.
collection PubMed
description Variability in disease development due to differences in strains and breeders constitutes a substantial challenge in preclinical research. However, the impact of the breeder on non-alcoholic steatohepatitis (NASH) is not yet fully elucidated. This retrospective study investigates NASH development in guinea pigs from Charles River or Envigo fed a high fat diet (20% fat, 15% sucrose, 0.35% cholesterol) for 16 or 24/25 weeks. Charles River animals displayed more severe NASH, with higher steatosis (p < 0.05 at week 16), inflammation (p < 0.05 at both week), fibrosis (p < 0.05 at week 16) and disease activity (p < 0.05 at both weeks). Accordingly, alanine and aspartate aminotransferase were increased at week 24/25 (p < 0.01). Hepatic expression of inflammatory (Ccl2, Cxcl8) and fibrotic (Pdgf, Serpine1, Col1a1) genes was also increased (p < 0.05). Differences were observed in healthy chow (4% fat, 0% sucrose, 0% cholesterol) fed animals: Envigo animals displayed higher relative liver weights (p < 0.01 at both weeks), liver cholesterol (p < 0.0001 at week 24/25) and aspartate aminotransferase (p < 0.05 at week 16), but lower levels of alkaline phosphatase (p < 0.0001 at week 24/25). These findings accentuates the importance of the breeder and its effect on NASH development and severity. Consequently, this may affect reproducibility, study comparison and limit the potential of developing novel therapies.
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spelling pubmed-78593972021-02-05 The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs Ipsen, D. H. Agerskov, R. H. Klaebel, J. H. Lykkesfeldt, J. Tveden-Nyborg, Pernille Sci Rep Article Variability in disease development due to differences in strains and breeders constitutes a substantial challenge in preclinical research. However, the impact of the breeder on non-alcoholic steatohepatitis (NASH) is not yet fully elucidated. This retrospective study investigates NASH development in guinea pigs from Charles River or Envigo fed a high fat diet (20% fat, 15% sucrose, 0.35% cholesterol) for 16 or 24/25 weeks. Charles River animals displayed more severe NASH, with higher steatosis (p < 0.05 at week 16), inflammation (p < 0.05 at both week), fibrosis (p < 0.05 at week 16) and disease activity (p < 0.05 at both weeks). Accordingly, alanine and aspartate aminotransferase were increased at week 24/25 (p < 0.01). Hepatic expression of inflammatory (Ccl2, Cxcl8) and fibrotic (Pdgf, Serpine1, Col1a1) genes was also increased (p < 0.05). Differences were observed in healthy chow (4% fat, 0% sucrose, 0% cholesterol) fed animals: Envigo animals displayed higher relative liver weights (p < 0.01 at both weeks), liver cholesterol (p < 0.0001 at week 24/25) and aspartate aminotransferase (p < 0.05 at week 16), but lower levels of alkaline phosphatase (p < 0.0001 at week 24/25). These findings accentuates the importance of the breeder and its effect on NASH development and severity. Consequently, this may affect reproducibility, study comparison and limit the potential of developing novel therapies. Nature Publishing Group UK 2021-02-03 /pmc/articles/PMC7859397/ /pubmed/33536590 http://dx.doi.org/10.1038/s41598-021-82643-0 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
Ipsen, D. H.
Agerskov, R. H.
Klaebel, J. H.
Lykkesfeldt, J.
Tveden-Nyborg, Pernille
The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
title The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
title_full The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
title_fullStr The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
title_full_unstemmed The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
title_short The development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
title_sort development of nonalcoholic steatohepatitis is subjected to breeder dependent variation in guinea pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859397/
https://www.ncbi.nlm.nih.gov/pubmed/33536590
http://dx.doi.org/10.1038/s41598-021-82643-0
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