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Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice
Imiquimod (IMQ)-induced skin inflammation is currently the most widely accepted psoriasis animal model, however, it features several limitations. We have modified the IMQ-model to minimize its systemic effects towards effectively maintaining the characteristic skin reactions. The original protocol (...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403245/ https://www.ncbi.nlm.nih.gov/pubmed/30842501 http://dx.doi.org/10.1038/s41598-019-39903-x |
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author | Horváth, Szabina Komlódi, Rita Perkecz, Anikó Pintér, Erika Gyulai, Rolland Kemény, Ágnes |
author_facet | Horváth, Szabina Komlódi, Rita Perkecz, Anikó Pintér, Erika Gyulai, Rolland Kemény, Ágnes |
author_sort | Horváth, Szabina |
collection | PubMed |
description | Imiquimod (IMQ)-induced skin inflammation is currently the most widely accepted psoriasis animal model, however, it features several limitations. We have modified the IMQ-model to minimize its systemic effects towards effectively maintaining the characteristic skin reactions. The original protocol (OP) uses 62.5 mg Aldara cream (or vaseline) on the shaved back skin of mice for 4 days. In contrast, in our modified protocol (MP) 25 mg Aldara and vaseline are applied simultaneously in separate Finn chambers over the dorsal skin of mice. In both the OP and MP groups, histology showed unequivocal hallmarks of psoriasiform dermatitis. Additionally, skin scaling and blood perfusion values were similar. While Aldara elicited significantly increased skin thickness in the MP group, significant weight loss, spleen enlargement, increased inflammatory cytokine levels in plasma, and treatment related death were only observed in the OP group. Our new method reproduces psoriatic skin alterations highlighting considerably reduced systemic inflammatory reactions. Possessing psoriasiform and control skin areas on the same mouse also reduces inter-individual differences. Additionally, the new method permits prolonged IMQ treatment studies to mimic the chronic nature of psoriasis. Finally, our experimental approach may also be used in other mouse models, to prevent the undesired systemic effects of topically applied drugs. |
format | Online Article Text |
id | pubmed-6403245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64032452019-03-08 Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice Horváth, Szabina Komlódi, Rita Perkecz, Anikó Pintér, Erika Gyulai, Rolland Kemény, Ágnes Sci Rep Article Imiquimod (IMQ)-induced skin inflammation is currently the most widely accepted psoriasis animal model, however, it features several limitations. We have modified the IMQ-model to minimize its systemic effects towards effectively maintaining the characteristic skin reactions. The original protocol (OP) uses 62.5 mg Aldara cream (or vaseline) on the shaved back skin of mice for 4 days. In contrast, in our modified protocol (MP) 25 mg Aldara and vaseline are applied simultaneously in separate Finn chambers over the dorsal skin of mice. In both the OP and MP groups, histology showed unequivocal hallmarks of psoriasiform dermatitis. Additionally, skin scaling and blood perfusion values were similar. While Aldara elicited significantly increased skin thickness in the MP group, significant weight loss, spleen enlargement, increased inflammatory cytokine levels in plasma, and treatment related death were only observed in the OP group. Our new method reproduces psoriatic skin alterations highlighting considerably reduced systemic inflammatory reactions. Possessing psoriasiform and control skin areas on the same mouse also reduces inter-individual differences. Additionally, the new method permits prolonged IMQ treatment studies to mimic the chronic nature of psoriasis. Finally, our experimental approach may also be used in other mouse models, to prevent the undesired systemic effects of topically applied drugs. Nature Publishing Group UK 2019-03-06 /pmc/articles/PMC6403245/ /pubmed/30842501 http://dx.doi.org/10.1038/s41598-019-39903-x Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Horváth, Szabina Komlódi, Rita Perkecz, Anikó Pintér, Erika Gyulai, Rolland Kemény, Ágnes Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice |
title | Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice |
title_full | Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice |
title_fullStr | Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice |
title_full_unstemmed | Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice |
title_short | Methodological refinement of Aldara-induced psoriasiform dermatitis model in mice |
title_sort | methodological refinement of aldara-induced psoriasiform dermatitis model in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403245/ https://www.ncbi.nlm.nih.gov/pubmed/30842501 http://dx.doi.org/10.1038/s41598-019-39903-x |
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