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Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice
BACKGROUND: Morus alba, a medicinal plant in Asia, has been used traditionally to treat diabetes mellitus and hypoglycemia. However, the effects of M. alba extract (MAE) on atopic dermatitis have not been verified scientifically. We investigated the effects of MAE on atopic dermatitis through in vit...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003291/ https://www.ncbi.nlm.nih.gov/pubmed/24755250 http://dx.doi.org/10.1186/1472-6882-14-139 |
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author | Lim, Hye-Sun Ha, Hyekyung Lee, Hoyoung Lee, Jun Kyung Lee, Mee-Young Shin, Hyeun-Kyoo |
author_facet | Lim, Hye-Sun Ha, Hyekyung Lee, Hoyoung Lee, Jun Kyung Lee, Mee-Young Shin, Hyeun-Kyoo |
author_sort | Lim, Hye-Sun |
collection | PubMed |
description | BACKGROUND: Morus alba, a medicinal plant in Asia, has been used traditionally to treat diabetes mellitus and hypoglycemia. However, the effects of M. alba extract (MAE) on atopic dermatitis have not been verified scientifically. We investigated the effects of MAE on atopic dermatitis through in vitro and in vivo experiments. METHODS: We evaluated the effects of MAE on the production of nitric oxide (NO) and prostaglandin E(2) (PGE(2)) in RAW 264.7, as well as thymus and activation-regulated chemokine (TARC/CCL17) in HaCaT cells. In an in vivo experiment, atopic dermatitis was induced by topical application of house dust mites for four weeks, and the protective effects of MAE were investigated by measuring the severity of the skin reaction on the back and ears, the plasma levels of immunoglobulin E (IgE) and histamine, and histopathological changes in the skin on the back and ears. RESULTS: MAE suppressed the production of NO and PGE(2) in RAW 264.7 cells, as well as TARC in HaCaT cells, in a dose-dependent manner. MAE treatment of NC/Nga mice reduced the severity of dermatitis and the plasma levels of IgE and histamine. MAE also reduced the histological manifestations of atopic dermatitis-like skin lesions such as erosion, hyperplasia of the epidermis and dermis, and inflammatory cell infiltration in the skin on the back and ears. CONCLUSION: Our results suggest that MAE has potent inhibitory effects on atopic dermatitis-like lesion and may be a beneficial natural resource for the treatment of atopic dermatitis. |
format | Online Article Text |
id | pubmed-4003291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40032912014-04-30 Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice Lim, Hye-Sun Ha, Hyekyung Lee, Hoyoung Lee, Jun Kyung Lee, Mee-Young Shin, Hyeun-Kyoo BMC Complement Altern Med Research Article BACKGROUND: Morus alba, a medicinal plant in Asia, has been used traditionally to treat diabetes mellitus and hypoglycemia. However, the effects of M. alba extract (MAE) on atopic dermatitis have not been verified scientifically. We investigated the effects of MAE on atopic dermatitis through in vitro and in vivo experiments. METHODS: We evaluated the effects of MAE on the production of nitric oxide (NO) and prostaglandin E(2) (PGE(2)) in RAW 264.7, as well as thymus and activation-regulated chemokine (TARC/CCL17) in HaCaT cells. In an in vivo experiment, atopic dermatitis was induced by topical application of house dust mites for four weeks, and the protective effects of MAE were investigated by measuring the severity of the skin reaction on the back and ears, the plasma levels of immunoglobulin E (IgE) and histamine, and histopathological changes in the skin on the back and ears. RESULTS: MAE suppressed the production of NO and PGE(2) in RAW 264.7 cells, as well as TARC in HaCaT cells, in a dose-dependent manner. MAE treatment of NC/Nga mice reduced the severity of dermatitis and the plasma levels of IgE and histamine. MAE also reduced the histological manifestations of atopic dermatitis-like skin lesions such as erosion, hyperplasia of the epidermis and dermis, and inflammatory cell infiltration in the skin on the back and ears. CONCLUSION: Our results suggest that MAE has potent inhibitory effects on atopic dermatitis-like lesion and may be a beneficial natural resource for the treatment of atopic dermatitis. BioMed Central 2014-04-23 /pmc/articles/PMC4003291/ /pubmed/24755250 http://dx.doi.org/10.1186/1472-6882-14-139 Text en Copyright © 2014 Lim et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Article Lim, Hye-Sun Ha, Hyekyung Lee, Hoyoung Lee, Jun Kyung Lee, Mee-Young Shin, Hyeun-Kyoo Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice |
title | Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice |
title_full | Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice |
title_fullStr | Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice |
title_full_unstemmed | Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice |
title_short | Morus alba L. suppresses the development of atopic dermatitis induced by the house dust mite in NC/Nga mice |
title_sort | morus alba l. suppresses the development of atopic dermatitis induced by the house dust mite in nc/nga mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003291/ https://www.ncbi.nlm.nih.gov/pubmed/24755250 http://dx.doi.org/10.1186/1472-6882-14-139 |
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