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Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice

The present study investigated the protective effects of Sargassum horneri (S. horneri) ethanol extract (SHE) against atopic dermatitis (AD), known as an abnormal immune response in house dust mite (HDM)/2,4-dinitrochlorobenzene (DNCB)-stimulated NC/Nga mice. The oral administration of SHE attenuate...

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Autores principales: Han, Eui Jeong, Fernando, Ilekuttige Priyan Shanura, Kim, Hyun-Soo, Jeon, You-Jin, Madusanka, Dissanayaka Mudiyanselage Dinesh, Dias, Mawalle Kankanamge Hasitha Madhawa, Jee, Youngheun, Ahn, Ginnae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468899/
https://www.ncbi.nlm.nih.gov/pubmed/32824648
http://dx.doi.org/10.3390/nu12082482
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author Han, Eui Jeong
Fernando, Ilekuttige Priyan Shanura
Kim, Hyun-Soo
Jeon, You-Jin
Madusanka, Dissanayaka Mudiyanselage Dinesh
Dias, Mawalle Kankanamge Hasitha Madhawa
Jee, Youngheun
Ahn, Ginnae
author_facet Han, Eui Jeong
Fernando, Ilekuttige Priyan Shanura
Kim, Hyun-Soo
Jeon, You-Jin
Madusanka, Dissanayaka Mudiyanselage Dinesh
Dias, Mawalle Kankanamge Hasitha Madhawa
Jee, Youngheun
Ahn, Ginnae
author_sort Han, Eui Jeong
collection PubMed
description The present study investigated the protective effects of Sargassum horneri (S. horneri) ethanol extract (SHE) against atopic dermatitis (AD), known as an abnormal immune response in house dust mite (HDM)/2,4-dinitrochlorobenzene (DNCB)-stimulated NC/Nga mice. The oral administration of SHE attenuated the AD symptoms, including the skin dermatitis severity, transepidermal water loss (TEWL), and ear edema in HDM/DNCB-stimulated mice. Moreover, the histological analysis revealed that SHE improved epidermal hyperplasia and hyperkeratosis, and reduced the dermal infiltrations of mast cells and eosinophils. Moreover, SHE downregulated the expression levels of cytokines (interleukin (IL)-6, IL-10, and interferon (IFN)-γ) and chemokines (Regulated on Activation, Normal T Cell Expressed and Secreted (RANTES), Eotaxin, and Thymus and activation-regulated chemokine (TARC)) by decreasing the expression levels of atopic initiators (IL-25 and IL-33) in HDM/DNCB-stimulated skin. The oral administration of SHE decreased the spleen size, reducing expression levels of AD-related cytokines (IL-4, IL-5, IL-6, IL-10, IL-13, IFN-γ, and TARC) by regulating the expressions of Tbx21 (T-bet), GATA Binding Protein 3 (GATA-3), and Signal transducer and activator of transcription 3 (STAT3). Moreover, SHE significantly attenuated the serum immunoglobulin (Ig)G(1) and IgG(2a) levels in HDM/DNCB-stimulated mice. Collectively, these results suggest that S. horneri could be an ingredient of functional food against abnormal immune response.
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spelling pubmed-74688992020-09-04 Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice Han, Eui Jeong Fernando, Ilekuttige Priyan Shanura Kim, Hyun-Soo Jeon, You-Jin Madusanka, Dissanayaka Mudiyanselage Dinesh Dias, Mawalle Kankanamge Hasitha Madhawa Jee, Youngheun Ahn, Ginnae Nutrients Article The present study investigated the protective effects of Sargassum horneri (S. horneri) ethanol extract (SHE) against atopic dermatitis (AD), known as an abnormal immune response in house dust mite (HDM)/2,4-dinitrochlorobenzene (DNCB)-stimulated NC/Nga mice. The oral administration of SHE attenuated the AD symptoms, including the skin dermatitis severity, transepidermal water loss (TEWL), and ear edema in HDM/DNCB-stimulated mice. Moreover, the histological analysis revealed that SHE improved epidermal hyperplasia and hyperkeratosis, and reduced the dermal infiltrations of mast cells and eosinophils. Moreover, SHE downregulated the expression levels of cytokines (interleukin (IL)-6, IL-10, and interferon (IFN)-γ) and chemokines (Regulated on Activation, Normal T Cell Expressed and Secreted (RANTES), Eotaxin, and Thymus and activation-regulated chemokine (TARC)) by decreasing the expression levels of atopic initiators (IL-25 and IL-33) in HDM/DNCB-stimulated skin. The oral administration of SHE decreased the spleen size, reducing expression levels of AD-related cytokines (IL-4, IL-5, IL-6, IL-10, IL-13, IFN-γ, and TARC) by regulating the expressions of Tbx21 (T-bet), GATA Binding Protein 3 (GATA-3), and Signal transducer and activator of transcription 3 (STAT3). Moreover, SHE significantly attenuated the serum immunoglobulin (Ig)G(1) and IgG(2a) levels in HDM/DNCB-stimulated mice. Collectively, these results suggest that S. horneri could be an ingredient of functional food against abnormal immune response. MDPI 2020-08-18 /pmc/articles/PMC7468899/ /pubmed/32824648 http://dx.doi.org/10.3390/nu12082482 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Han, Eui Jeong
Fernando, Ilekuttige Priyan Shanura
Kim, Hyun-Soo
Jeon, You-Jin
Madusanka, Dissanayaka Mudiyanselage Dinesh
Dias, Mawalle Kankanamge Hasitha Madhawa
Jee, Youngheun
Ahn, Ginnae
Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice
title Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice
title_full Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice
title_fullStr Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice
title_full_unstemmed Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice
title_short Oral Administration of Sargassum horneri Improves the HDM/DNCB-Induced Atopic Dermatitis in NC/Nga Mice
title_sort oral administration of sargassum horneri improves the hdm/dncb-induced atopic dermatitis in nc/nga mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468899/
https://www.ncbi.nlm.nih.gov/pubmed/32824648
http://dx.doi.org/10.3390/nu12082482
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