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Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse

Atopic dermatitis (AD) is an inflammatory skin disease characterized by intense pruritus and relapsable eczematous lesions. The hallmarks of AD are defects in the epidermal barrier and immunoglobulin E (IgE)-mediated sensitization to several environmental allergens, as well as an immune disorder med...

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Autores principales: Kim, Woon-Hae, An, Hyun-Jin, Kim, Jung-Yeon, Gwon, Mi-Gyeong, Gu, Hyemin, Jeon, Minji, Sung, Woo Jung, Han, Sang Mi, Pak, Sok Cheon, Kim, Min-Kyung, Park, Kwan-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732199/
https://www.ncbi.nlm.nih.gov/pubmed/29247241
http://dx.doi.org/10.1038/s41598-017-17873-2
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author Kim, Woon-Hae
An, Hyun-Jin
Kim, Jung-Yeon
Gwon, Mi-Gyeong
Gu, Hyemin
Jeon, Minji
Sung, Woo Jung
Han, Sang Mi
Pak, Sok Cheon
Kim, Min-Kyung
Park, Kwan-Kyu
author_facet Kim, Woon-Hae
An, Hyun-Jin
Kim, Jung-Yeon
Gwon, Mi-Gyeong
Gu, Hyemin
Jeon, Minji
Sung, Woo Jung
Han, Sang Mi
Pak, Sok Cheon
Kim, Min-Kyung
Park, Kwan-Kyu
author_sort Kim, Woon-Hae
collection PubMed
description Atopic dermatitis (AD) is an inflammatory skin disease characterized by intense pruritus and relapsable eczematous lesions. The hallmarks of AD are defects in the epidermal barrier and immunoglobulin E (IgE)-mediated sensitization to several environmental allergens, as well as an immune disorder mediated by an imbalance toward T-helper-2 response. Melittin, a major component of bee venom, has been studied in various inflammatory diseases. However, the beneficial effects of melittin on mouse with AD-like symptoms have not been explored. Therefore, we investigated the anti-allergic effects of melittin. AD was induced by ovalbumin (OVA) patch. After agent treatment, skin tissues and sera were extracted from the sacrificed mice were used to demonstrate the effects of melittin through various molecular biological methods. The results showed that OVA-induced skin thickening and inflammatory infiltration were decreased in the melittin-treated group. Melittin prevented OVA-induced filaggrin deficiency and imbalanced inflammatory mediators. Furthermore, melittin inhibited IL-4/IL-13-induced filaggrin downregulation through the blockade of STAT3 activation in human keratinocytes. In summary, this study has shown that melittin ameliorated OVA-induced AD-like symptoms from various perspectives. The findings of this study may be the first evidence of the anti-inflammatory effects of melittin on OVA-induced AD.
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spelling pubmed-57321992017-12-21 Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse Kim, Woon-Hae An, Hyun-Jin Kim, Jung-Yeon Gwon, Mi-Gyeong Gu, Hyemin Jeon, Minji Sung, Woo Jung Han, Sang Mi Pak, Sok Cheon Kim, Min-Kyung Park, Kwan-Kyu Sci Rep Article Atopic dermatitis (AD) is an inflammatory skin disease characterized by intense pruritus and relapsable eczematous lesions. The hallmarks of AD are defects in the epidermal barrier and immunoglobulin E (IgE)-mediated sensitization to several environmental allergens, as well as an immune disorder mediated by an imbalance toward T-helper-2 response. Melittin, a major component of bee venom, has been studied in various inflammatory diseases. However, the beneficial effects of melittin on mouse with AD-like symptoms have not been explored. Therefore, we investigated the anti-allergic effects of melittin. AD was induced by ovalbumin (OVA) patch. After agent treatment, skin tissues and sera were extracted from the sacrificed mice were used to demonstrate the effects of melittin through various molecular biological methods. The results showed that OVA-induced skin thickening and inflammatory infiltration were decreased in the melittin-treated group. Melittin prevented OVA-induced filaggrin deficiency and imbalanced inflammatory mediators. Furthermore, melittin inhibited IL-4/IL-13-induced filaggrin downregulation through the blockade of STAT3 activation in human keratinocytes. In summary, this study has shown that melittin ameliorated OVA-induced AD-like symptoms from various perspectives. The findings of this study may be the first evidence of the anti-inflammatory effects of melittin on OVA-induced AD. Nature Publishing Group UK 2017-12-15 /pmc/articles/PMC5732199/ /pubmed/29247241 http://dx.doi.org/10.1038/s41598-017-17873-2 Text en © The Author(s) 2017 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
Kim, Woon-Hae
An, Hyun-Jin
Kim, Jung-Yeon
Gwon, Mi-Gyeong
Gu, Hyemin
Jeon, Minji
Sung, Woo Jung
Han, Sang Mi
Pak, Sok Cheon
Kim, Min-Kyung
Park, Kwan-Kyu
Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
title Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
title_full Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
title_fullStr Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
title_full_unstemmed Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
title_short Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
title_sort beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732199/
https://www.ncbi.nlm.nih.gov/pubmed/29247241
http://dx.doi.org/10.1038/s41598-017-17873-2
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