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Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model
Severity assessment in laboratory animals is an important issue regarding the implementation of the 3R concept into biomedical research and pivotal in current EU regulations. In mouse models of inflammatory bowel disease severity assessment is usually undertaken by clinical scoring, especially by mo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670219/ https://www.ncbi.nlm.nih.gov/pubmed/26637175 http://dx.doi.org/10.1371/journal.pone.0143824 |
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author | Häger, Christine Keubler, Lydia M. Biernot, Svenja Dietrich, Jana Buchheister, Stephanie Buettner, Manuela Bleich, André |
author_facet | Häger, Christine Keubler, Lydia M. Biernot, Svenja Dietrich, Jana Buchheister, Stephanie Buettner, Manuela Bleich, André |
author_sort | Häger, Christine |
collection | PubMed |
description | Severity assessment in laboratory animals is an important issue regarding the implementation of the 3R concept into biomedical research and pivotal in current EU regulations. In mouse models of inflammatory bowel disease severity assessment is usually undertaken by clinical scoring, especially by monitoring reduction of body weight. This requires daily observance and handling of each mouse, which is time consuming, stressful for the animal and necessitates an experienced observer. The time to integrate to nest test (TINT) is an easily applicable test detecting disturbed welfare by measuring the time interval mice need to integrate nesting material to an existing nest. Here, TINT was utilized to assess severity in a mouse DSS-colitis model. TINT results depended on the group size of mice maintained per cage with most consistent time intervals measured when co-housing 4 to 5 mice. Colitis was induced with 1% or 1.5% DSS in group-housed WT and Cd14-deficient mice. Higher clinical scores and loss of body weight were detected in 1.5% compared to 1% DSS treated mice. TINT time intervals showed no dose dependent differences. However, increased clinical scores, body weight reductions, and increased TINT time intervals were detected in Cd14 (-/-) compared to WT mice revealing mouse strain related differences. Therefore, TINT is an easily applicable method for severity assessment in a mouse colitis model detecting CD14 related differences, but not dose dependent differences. As TINT revealed most consistent results in group-housed mice, we recommend utilization as an additional method substituting clinical monitoring of the individual mouse. |
format | Online Article Text |
id | pubmed-4670219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46702192015-12-10 Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model Häger, Christine Keubler, Lydia M. Biernot, Svenja Dietrich, Jana Buchheister, Stephanie Buettner, Manuela Bleich, André PLoS One Research Article Severity assessment in laboratory animals is an important issue regarding the implementation of the 3R concept into biomedical research and pivotal in current EU regulations. In mouse models of inflammatory bowel disease severity assessment is usually undertaken by clinical scoring, especially by monitoring reduction of body weight. This requires daily observance and handling of each mouse, which is time consuming, stressful for the animal and necessitates an experienced observer. The time to integrate to nest test (TINT) is an easily applicable test detecting disturbed welfare by measuring the time interval mice need to integrate nesting material to an existing nest. Here, TINT was utilized to assess severity in a mouse DSS-colitis model. TINT results depended on the group size of mice maintained per cage with most consistent time intervals measured when co-housing 4 to 5 mice. Colitis was induced with 1% or 1.5% DSS in group-housed WT and Cd14-deficient mice. Higher clinical scores and loss of body weight were detected in 1.5% compared to 1% DSS treated mice. TINT time intervals showed no dose dependent differences. However, increased clinical scores, body weight reductions, and increased TINT time intervals were detected in Cd14 (-/-) compared to WT mice revealing mouse strain related differences. Therefore, TINT is an easily applicable method for severity assessment in a mouse colitis model detecting CD14 related differences, but not dose dependent differences. As TINT revealed most consistent results in group-housed mice, we recommend utilization as an additional method substituting clinical monitoring of the individual mouse. Public Library of Science 2015-12-04 /pmc/articles/PMC4670219/ /pubmed/26637175 http://dx.doi.org/10.1371/journal.pone.0143824 Text en © 2015 Häger et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Häger, Christine Keubler, Lydia M. Biernot, Svenja Dietrich, Jana Buchheister, Stephanie Buettner, Manuela Bleich, André Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model |
title | Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model |
title_full | Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model |
title_fullStr | Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model |
title_full_unstemmed | Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model |
title_short | Time to Integrate to Nest Test Evaluation in a Mouse DSS-Colitis Model |
title_sort | time to integrate to nest test evaluation in a mouse dss-colitis model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670219/ https://www.ncbi.nlm.nih.gov/pubmed/26637175 http://dx.doi.org/10.1371/journal.pone.0143824 |
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