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Lessons learned: optimization of a murine small bowel resection model()()
PURPOSE: Central to the use of murine models of disease is the ability to derive reproducible data. The purpose of this study was to determine factors contributing to variability in our murine model of small bowel resection (SBR). METHODS: Male C57Bl/6 mice were randomized to sham or 50% SBR. The ef...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481288/ https://www.ncbi.nlm.nih.gov/pubmed/18558176 http://dx.doi.org/10.1016/j.jpedsurg.2008.02.025 |
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author | Taylor, Janice A. Martin, Colin A. Nair, Rajalakshmi Guo, Jun Erwin, Christopher R. Warner, Brad W. |
author_facet | Taylor, Janice A. Martin, Colin A. Nair, Rajalakshmi Guo, Jun Erwin, Christopher R. Warner, Brad W. |
author_sort | Taylor, Janice A. |
collection | PubMed |
description | PURPOSE: Central to the use of murine models of disease is the ability to derive reproducible data. The purpose of this study was to determine factors contributing to variability in our murine model of small bowel resection (SBR). METHODS: Male C57Bl/6 mice were randomized to sham or 50% SBR. The effect of housing type (pathogen-free vs standard housing), nutrition (reconstituted powder vs tube feeding formulation), and correlates of intestinal morphology with gene expression changes were investigated. Multiple linear regression modeling or 1-way analysis of variance was used for data analysis. RESULTS: Pathogen-free mice had significantly shorter ileal villi at baseline and demonstrated greater villus growth after SBR compared to mice housed in standard rooms. Food type did not affect adaptation. Gene expression changes were more consistent and significant in isolated crypt cells that demonstrated adaptive growth when compared with crypts that did not deepen after SBR. CONCLUSION: Maintenance of mice in pathogen-free conditions and restricting gene expression analysis to individual animals exhibiting morphologic adaptation enhances sensitivity and specificity of data derived from this model. These refinements will minimize experimental variability and lead to improved understanding of the complex process of intestinal adaptation. |
format | Text |
id | pubmed-2481288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-24812882009-06-01 Lessons learned: optimization of a murine small bowel resection model()() Taylor, Janice A. Martin, Colin A. Nair, Rajalakshmi Guo, Jun Erwin, Christopher R. Warner, Brad W. J Pediatr Surg AAP Paper PURPOSE: Central to the use of murine models of disease is the ability to derive reproducible data. The purpose of this study was to determine factors contributing to variability in our murine model of small bowel resection (SBR). METHODS: Male C57Bl/6 mice were randomized to sham or 50% SBR. The effect of housing type (pathogen-free vs standard housing), nutrition (reconstituted powder vs tube feeding formulation), and correlates of intestinal morphology with gene expression changes were investigated. Multiple linear regression modeling or 1-way analysis of variance was used for data analysis. RESULTS: Pathogen-free mice had significantly shorter ileal villi at baseline and demonstrated greater villus growth after SBR compared to mice housed in standard rooms. Food type did not affect adaptation. Gene expression changes were more consistent and significant in isolated crypt cells that demonstrated adaptive growth when compared with crypts that did not deepen after SBR. CONCLUSION: Maintenance of mice in pathogen-free conditions and restricting gene expression analysis to individual animals exhibiting morphologic adaptation enhances sensitivity and specificity of data derived from this model. These refinements will minimize experimental variability and lead to improved understanding of the complex process of intestinal adaptation. Elsevier Inc. 2008-06 2008-06-14 /pmc/articles/PMC2481288/ /pubmed/18558176 http://dx.doi.org/10.1016/j.jpedsurg.2008.02.025 Text en Copyright © 2008 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | AAP Paper Taylor, Janice A. Martin, Colin A. Nair, Rajalakshmi Guo, Jun Erwin, Christopher R. Warner, Brad W. Lessons learned: optimization of a murine small bowel resection model()() |
title | Lessons learned: optimization of a murine small bowel resection model()() |
title_full | Lessons learned: optimization of a murine small bowel resection model()() |
title_fullStr | Lessons learned: optimization of a murine small bowel resection model()() |
title_full_unstemmed | Lessons learned: optimization of a murine small bowel resection model()() |
title_short | Lessons learned: optimization of a murine small bowel resection model()() |
title_sort | lessons learned: optimization of a murine small bowel resection model()() |
topic | AAP Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481288/ https://www.ncbi.nlm.nih.gov/pubmed/18558176 http://dx.doi.org/10.1016/j.jpedsurg.2008.02.025 |
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