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Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression
Atopic dermatitis (AD) is a chronic inflammatory skin disease in which skin barrier dysfunction leads to dryness, pruritus, and erythematous lesions. AD is triggered by immune imbalance and oxidative stress. Echinochrome A (Ech A), a natural pigment isolated from sea urchins, exerts antioxidant and...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625509/ https://www.ncbi.nlm.nih.gov/pubmed/34822493 http://dx.doi.org/10.3390/md19110622 |
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author | Yun, Hyeong Rok Ahn, Sang Woo Seol, Bomin Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin Ko, Kyung Soo Rhee, Byoung Doo Seol, Jung Eun Kim, Hyoung Kyu |
author_facet | Yun, Hyeong Rok Ahn, Sang Woo Seol, Bomin Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin Ko, Kyung Soo Rhee, Byoung Doo Seol, Jung Eun Kim, Hyoung Kyu |
author_sort | Yun, Hyeong Rok |
collection | PubMed |
description | Atopic dermatitis (AD) is a chronic inflammatory skin disease in which skin barrier dysfunction leads to dryness, pruritus, and erythematous lesions. AD is triggered by immune imbalance and oxidative stress. Echinochrome A (Ech A), a natural pigment isolated from sea urchins, exerts antioxidant and beneficial effects in various inflammatory disease models. In the present study, we tested whether Ech A treatment alleviated AD-like skin lesions. We examined the anti-inflammatory effect of Ech A on 2,4-dinitrochlorobenzene (DNCB)-induced AD-like lesions in an NC/Nga mouse model. AD-like skin symptoms were induced by treatment with 1% DNCB for 1 week and 0.4% DNCB for 5 weeks in NC/Nga mice. The results showed that Ech A alleviated AD clinical symptoms, such as edema, erythema, and dryness. Treatment with Ech A induced the recovery of epidermis skin lesions as observed histologically. Tewameter(®) and Corneometer(®) measurements indicated that Ech A treatment reduced transepidermal water loss and improved stratum corneum hydration, respectively. Ech A treatment also inhibited inflammatory-response-induced mast cell infiltration in AD-like skin lesions and suppressed the expression of proinflammatory cytokines, such as interferon-γ, interleukin-4, and interleukin-13. Collectively, these results suggest that Ech A may be beneficial for treating AD owing to its anti-inflammatory effects. |
format | Online Article Text |
id | pubmed-8625509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86255092021-11-27 Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression Yun, Hyeong Rok Ahn, Sang Woo Seol, Bomin Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin Ko, Kyung Soo Rhee, Byoung Doo Seol, Jung Eun Kim, Hyoung Kyu Mar Drugs Article Atopic dermatitis (AD) is a chronic inflammatory skin disease in which skin barrier dysfunction leads to dryness, pruritus, and erythematous lesions. AD is triggered by immune imbalance and oxidative stress. Echinochrome A (Ech A), a natural pigment isolated from sea urchins, exerts antioxidant and beneficial effects in various inflammatory disease models. In the present study, we tested whether Ech A treatment alleviated AD-like skin lesions. We examined the anti-inflammatory effect of Ech A on 2,4-dinitrochlorobenzene (DNCB)-induced AD-like lesions in an NC/Nga mouse model. AD-like skin symptoms were induced by treatment with 1% DNCB for 1 week and 0.4% DNCB for 5 weeks in NC/Nga mice. The results showed that Ech A alleviated AD clinical symptoms, such as edema, erythema, and dryness. Treatment with Ech A induced the recovery of epidermis skin lesions as observed histologically. Tewameter(®) and Corneometer(®) measurements indicated that Ech A treatment reduced transepidermal water loss and improved stratum corneum hydration, respectively. Ech A treatment also inhibited inflammatory-response-induced mast cell infiltration in AD-like skin lesions and suppressed the expression of proinflammatory cytokines, such as interferon-γ, interleukin-4, and interleukin-13. Collectively, these results suggest that Ech A may be beneficial for treating AD owing to its anti-inflammatory effects. MDPI 2021-11-01 /pmc/articles/PMC8625509/ /pubmed/34822493 http://dx.doi.org/10.3390/md19110622 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yun, Hyeong Rok Ahn, Sang Woo Seol, Bomin Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin Ko, Kyung Soo Rhee, Byoung Doo Seol, Jung Eun Kim, Hyoung Kyu Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression |
title | Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression |
title_full | Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression |
title_fullStr | Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression |
title_full_unstemmed | Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression |
title_short | Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression |
title_sort | echinochrome a treatment alleviates atopic dermatitis-like skin lesions in nc/nga mice via il-4 and il-13 suppression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625509/ https://www.ncbi.nlm.nih.gov/pubmed/34822493 http://dx.doi.org/10.3390/md19110622 |
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