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Severity assessment in mice subjected to carbon tetrachloride
The Directive 2010/63 EU requires classifying burden and severity in all procedures using laboratory animals. This study evaluated the severity of liver fibrosis induction by intraperitoneal carbon tetrachloride (CCl(4)) injections in mice. 29 male C57BL/6N mice were treated three times per week for...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519684/ https://www.ncbi.nlm.nih.gov/pubmed/32978437 http://dx.doi.org/10.1038/s41598-020-72801-1 |
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author | Ernst, Lisa Zieglowski, Leonie Schulz, Mareike Moss, Michaela Meyer, Marco Weiskirchen, Ralf Palme, Rupert Hamann, Melanie Talbot, Steven R. Tolba, René H. |
author_facet | Ernst, Lisa Zieglowski, Leonie Schulz, Mareike Moss, Michaela Meyer, Marco Weiskirchen, Ralf Palme, Rupert Hamann, Melanie Talbot, Steven R. Tolba, René H. |
author_sort | Ernst, Lisa |
collection | PubMed |
description | The Directive 2010/63 EU requires classifying burden and severity in all procedures using laboratory animals. This study evaluated the severity of liver fibrosis induction by intraperitoneal carbon tetrachloride (CCl(4)) injections in mice. 29 male C57BL/6N mice were treated three times per week for 4 weeks with an intraperitoneal injection (50 µl) of either 0.6 ml/kg body weight CCl(4)-vehicle solution, germ oil (vehicle-control) or handling only. Severity assessment was performed using serum analysis, behavioral tests (open field test, rotarod, burrowing and nesting behavior), fecal corticosterone metabolite (FCM) measurement, and survival. The most significant group differences were noticed in the second week of treatment when the highest AST (1463 ± 1404 vs. 123.8 ± 93 U/L, p < 0.0001) and nesting values were measured. In addition, respective animals showed lower moving distances (4622 ± 1577 vs. 6157 ± 2060 cm, p < 0.01) and velocity in the Open field, identified as main factors in principal component analysis (PCA). Overall, a 50% survival rate was observed within the treatment group, in which the open field performance was a good tracer parameter for survival. In summary, this study demonstrates the feasibility of assessing severity in mice using behavioral tests and highlight the open field test as a possible threshold parameter for risk assessment of mortality. |
format | Online Article Text |
id | pubmed-7519684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75196842020-09-29 Severity assessment in mice subjected to carbon tetrachloride Ernst, Lisa Zieglowski, Leonie Schulz, Mareike Moss, Michaela Meyer, Marco Weiskirchen, Ralf Palme, Rupert Hamann, Melanie Talbot, Steven R. Tolba, René H. Sci Rep Article The Directive 2010/63 EU requires classifying burden and severity in all procedures using laboratory animals. This study evaluated the severity of liver fibrosis induction by intraperitoneal carbon tetrachloride (CCl(4)) injections in mice. 29 male C57BL/6N mice were treated three times per week for 4 weeks with an intraperitoneal injection (50 µl) of either 0.6 ml/kg body weight CCl(4)-vehicle solution, germ oil (vehicle-control) or handling only. Severity assessment was performed using serum analysis, behavioral tests (open field test, rotarod, burrowing and nesting behavior), fecal corticosterone metabolite (FCM) measurement, and survival. The most significant group differences were noticed in the second week of treatment when the highest AST (1463 ± 1404 vs. 123.8 ± 93 U/L, p < 0.0001) and nesting values were measured. In addition, respective animals showed lower moving distances (4622 ± 1577 vs. 6157 ± 2060 cm, p < 0.01) and velocity in the Open field, identified as main factors in principal component analysis (PCA). Overall, a 50% survival rate was observed within the treatment group, in which the open field performance was a good tracer parameter for survival. In summary, this study demonstrates the feasibility of assessing severity in mice using behavioral tests and highlight the open field test as a possible threshold parameter for risk assessment of mortality. Nature Publishing Group UK 2020-09-25 /pmc/articles/PMC7519684/ /pubmed/32978437 http://dx.doi.org/10.1038/s41598-020-72801-1 Text en © The Author(s) 2020 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 Ernst, Lisa Zieglowski, Leonie Schulz, Mareike Moss, Michaela Meyer, Marco Weiskirchen, Ralf Palme, Rupert Hamann, Melanie Talbot, Steven R. Tolba, René H. Severity assessment in mice subjected to carbon tetrachloride |
title | Severity assessment in mice subjected to carbon tetrachloride |
title_full | Severity assessment in mice subjected to carbon tetrachloride |
title_fullStr | Severity assessment in mice subjected to carbon tetrachloride |
title_full_unstemmed | Severity assessment in mice subjected to carbon tetrachloride |
title_short | Severity assessment in mice subjected to carbon tetrachloride |
title_sort | severity assessment in mice subjected to carbon tetrachloride |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519684/ https://www.ncbi.nlm.nih.gov/pubmed/32978437 http://dx.doi.org/10.1038/s41598-020-72801-1 |
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