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An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model
The cuprizone model is a well-established and investigated paradigm to study demyelination and remyelination in rodents. Cuprizone is usually administrated by mixing in the powdered or pelleted rodent chow. However, since cuprizone is sensitive to the environment and the consumption of it varies bet...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574485/ https://www.ncbi.nlm.nih.gov/pubmed/28840755 http://dx.doi.org/10.1177/1759091417725174 |
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author | Zhen, Wei Liu, Ailian Lu, Jiaqi Zhang, Wandong Tattersall, David Wang, Jianfei |
author_facet | Zhen, Wei Liu, Ailian Lu, Jiaqi Zhang, Wandong Tattersall, David Wang, Jianfei |
author_sort | Zhen, Wei |
collection | PubMed |
description | The cuprizone model is a well-established and investigated paradigm to study demyelination and remyelination in rodents. Cuprizone is usually administrated by mixing in the powdered or pelleted rodent chow. However, since cuprizone is sensitive to the environment and the consumption of it varies between different animals, the major issue is the discrepancy in demyelination of the animals. This study reports the development of the cuprizone model by gavage administrations in mice. Following testing a series of doses of cuprizone, 400 mg/kg/day was found to be the best dosage to induce dramatic and consistent demyelination after 5 weeks of administration; while remyelination quickly occurred after 9 days of cuprizone withdrawal. The advantage of this alternative model is that the consumption of cuprizone could be well controlled, and the mice were exposed to the same dose of cuprizone. Thus, the variation in demyelination was minimized. This alternative cuprizone dosing regime minimizes the interanimal variability on demyelination and hence provides a consistent model for pharmacological evaluations, in addition to reducing the number of animals used in the experiments. |
format | Online Article Text |
id | pubmed-5574485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55744852017-09-08 An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model Zhen, Wei Liu, Ailian Lu, Jiaqi Zhang, Wandong Tattersall, David Wang, Jianfei ASN Neuro Original Paper The cuprizone model is a well-established and investigated paradigm to study demyelination and remyelination in rodents. Cuprizone is usually administrated by mixing in the powdered or pelleted rodent chow. However, since cuprizone is sensitive to the environment and the consumption of it varies between different animals, the major issue is the discrepancy in demyelination of the animals. This study reports the development of the cuprizone model by gavage administrations in mice. Following testing a series of doses of cuprizone, 400 mg/kg/day was found to be the best dosage to induce dramatic and consistent demyelination after 5 weeks of administration; while remyelination quickly occurred after 9 days of cuprizone withdrawal. The advantage of this alternative model is that the consumption of cuprizone could be well controlled, and the mice were exposed to the same dose of cuprizone. Thus, the variation in demyelination was minimized. This alternative cuprizone dosing regime minimizes the interanimal variability on demyelination and hence provides a consistent model for pharmacological evaluations, in addition to reducing the number of animals used in the experiments. SAGE Publications 2017-08-25 /pmc/articles/PMC5574485/ /pubmed/28840755 http://dx.doi.org/10.1177/1759091417725174 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Paper Zhen, Wei Liu, Ailian Lu, Jiaqi Zhang, Wandong Tattersall, David Wang, Jianfei An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model |
title | An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model |
title_full | An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model |
title_fullStr | An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model |
title_full_unstemmed | An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model |
title_short | An Alternative Cuprizone-Induced Demyelination and Remyelination Mouse Model |
title_sort | alternative cuprizone-induced demyelination and remyelination mouse model |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574485/ https://www.ncbi.nlm.nih.gov/pubmed/28840755 http://dx.doi.org/10.1177/1759091417725174 |
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