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Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice

OBJECTIVE: Atopic dermatitis (AD) is a chronic inflammatory skin disease mainly caused by immune stimuli. The current study was conducted to investigate the effects of ROCEN and to compare it with betamethasone (Beta) on mice subjected to AD. METHODS: First, the safety of topical ROCEN was tested to...

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Autores principales: Goudarzi, Ramin, Eskandarynasab, Maryam, Muhammadnejad, Ahad, Dehpour, Ahmad Reza, Partoazar, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422727/
https://www.ncbi.nlm.nih.gov/pubmed/34488737
http://dx.doi.org/10.1186/s12906-021-03393-0
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author Goudarzi, Ramin
Eskandarynasab, Maryam
Muhammadnejad, Ahad
Dehpour, Ahmad Reza
Partoazar, Alireza
author_facet Goudarzi, Ramin
Eskandarynasab, Maryam
Muhammadnejad, Ahad
Dehpour, Ahmad Reza
Partoazar, Alireza
author_sort Goudarzi, Ramin
collection PubMed
description OBJECTIVE: Atopic dermatitis (AD) is a chronic inflammatory skin disease mainly caused by immune stimuli. The current study was conducted to investigate the effects of ROCEN and to compare it with betamethasone (Beta) on mice subjected to AD. METHODS: First, the safety of topical ROCEN was tested to determine possible sensitization induction in vivo. Then, the mice were subjected to oxazolone (Oxa) to induce chronic AD. Consequently, they underwent treatment with ROCEN and Beta. Scratching and wiping behaviors related to dermatitis were evaluated in treated animals for 35 days. The histopathology and immunohistochemistry (IHC) analysis of interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α) cytokines were performed on the dorsal skin of the treated mice. RESULTS: Topical administration of ROCEN and Beta to the dorsum of sensitized mice for 5 weeks significantly alleviated scratching and wiping symptoms and reduced erythema, scaling, and edema in the skin of the mice with AD. Moreover, histological indices showed that ROCEN effectively reduced leucocyte infiltration and improved skin healing parameters in treated AD mice. Application of ROCEN or Beta reduced IHC markers including IL-8 and TNF-α significantly. CONCLUSION: ROCEN alleviated the AD symptoms similar to betamethasone in an experimental animal model.
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spelling pubmed-84227272021-09-09 Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice Goudarzi, Ramin Eskandarynasab, Maryam Muhammadnejad, Ahad Dehpour, Ahmad Reza Partoazar, Alireza BMC Complement Med Ther Research OBJECTIVE: Atopic dermatitis (AD) is a chronic inflammatory skin disease mainly caused by immune stimuli. The current study was conducted to investigate the effects of ROCEN and to compare it with betamethasone (Beta) on mice subjected to AD. METHODS: First, the safety of topical ROCEN was tested to determine possible sensitization induction in vivo. Then, the mice were subjected to oxazolone (Oxa) to induce chronic AD. Consequently, they underwent treatment with ROCEN and Beta. Scratching and wiping behaviors related to dermatitis were evaluated in treated animals for 35 days. The histopathology and immunohistochemistry (IHC) analysis of interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α) cytokines were performed on the dorsal skin of the treated mice. RESULTS: Topical administration of ROCEN and Beta to the dorsum of sensitized mice for 5 weeks significantly alleviated scratching and wiping symptoms and reduced erythema, scaling, and edema in the skin of the mice with AD. Moreover, histological indices showed that ROCEN effectively reduced leucocyte infiltration and improved skin healing parameters in treated AD mice. Application of ROCEN or Beta reduced IHC markers including IL-8 and TNF-α significantly. CONCLUSION: ROCEN alleviated the AD symptoms similar to betamethasone in an experimental animal model. BioMed Central 2021-09-06 /pmc/articles/PMC8422727/ /pubmed/34488737 http://dx.doi.org/10.1186/s12906-021-03393-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Goudarzi, Ramin
Eskandarynasab, Maryam
Muhammadnejad, Ahad
Dehpour, Ahmad Reza
Partoazar, Alireza
Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice
title Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice
title_full Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice
title_fullStr Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice
title_full_unstemmed Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice
title_short Beneficial effects of ROCEN (Topical Nano-arthrocen) on atopic dermatitis in mice
title_sort beneficial effects of rocen (topical nano-arthrocen) on atopic dermatitis in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422727/
https://www.ncbi.nlm.nih.gov/pubmed/34488737
http://dx.doi.org/10.1186/s12906-021-03393-0
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