Cargando…

Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma

Dihydromyricetin (DHM) is a plant flavonoid and is the primary active ingredient isolated from the medicinal herb, Ampelopsis grossedentata. DHM has been shown to possess various pharmacological activities, including anti-inflammatory effects. However, the possible role of DHM in asthma treatment re...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Bin, Huang, Shuran, Wang, Caiying, Zhang, Haitao, Fang, Shengcun, Zhang, Yingming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436282/
https://www.ncbi.nlm.nih.gov/pubmed/28393183
http://dx.doi.org/10.3892/mmr.2017.6428
_version_ 1783237370138591232
author Xu, Bin
Huang, Shuran
Wang, Caiying
Zhang, Haitao
Fang, Shengcun
Zhang, Yingming
author_facet Xu, Bin
Huang, Shuran
Wang, Caiying
Zhang, Haitao
Fang, Shengcun
Zhang, Yingming
author_sort Xu, Bin
collection PubMed
description Dihydromyricetin (DHM) is a plant flavonoid and is the primary active ingredient isolated from the medicinal herb, Ampelopsis grossedentata. DHM has been shown to possess various pharmacological activities, including anti-inflammatory effects. However, the possible role of DHM in asthma treatment remains to be elucidated. The present study aimed to investigate its anti-inflammatory properties in mice with symptoms of allergic asthma. The C57BL/6 mice were sensitized and challenged with ovalbumin (OVA) to induce asthma. DHM or phosphate-buffered saline treatment was administered 1 h prior to the OVA challenge. The levels of interleukin (IL)-4, IL-5 and IL-13 in the bronchoalveolar lavage (BAL) fluid were measured by enzyme-linked immunosorbent assay (ELISA), and OVA-specific serum IgE and IgG1 levels were also determined by ELISA. Histopathological staining was performed to evaluate the infiltration of inflammatory cells into the BAL fluid, lung tissues and goblet cell hyperplasia. DHM treatment significantly reduced the total number of inflammatory cells, including eosinophils, neutrophils, lymphocytes and macrophages, in the BAL fluid. DHM also reduced the levels of IL-4, IL-5 and IL-13 in the BAL fluid, and reduced the secretion of OVA-specific IgE and IgG1 in the serum. The histological staining demonstrated that DHM treatment effectively suppressed the OVA-induced inflammatory cells in the lung tissues and in the mucus hypersecreted by goblet cells in the airway. These results showed that DHM had a potent anti-inflammatory effect in an OVA-induced mouse model of asthma, offering potential as an anti-inflammatory agent for the treatment of asthma.
format Online
Article
Text
id pubmed-5436282
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-54362822017-05-19 Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma Xu, Bin Huang, Shuran Wang, Caiying Zhang, Haitao Fang, Shengcun Zhang, Yingming Mol Med Rep Articles Dihydromyricetin (DHM) is a plant flavonoid and is the primary active ingredient isolated from the medicinal herb, Ampelopsis grossedentata. DHM has been shown to possess various pharmacological activities, including anti-inflammatory effects. However, the possible role of DHM in asthma treatment remains to be elucidated. The present study aimed to investigate its anti-inflammatory properties in mice with symptoms of allergic asthma. The C57BL/6 mice were sensitized and challenged with ovalbumin (OVA) to induce asthma. DHM or phosphate-buffered saline treatment was administered 1 h prior to the OVA challenge. The levels of interleukin (IL)-4, IL-5 and IL-13 in the bronchoalveolar lavage (BAL) fluid were measured by enzyme-linked immunosorbent assay (ELISA), and OVA-specific serum IgE and IgG1 levels were also determined by ELISA. Histopathological staining was performed to evaluate the infiltration of inflammatory cells into the BAL fluid, lung tissues and goblet cell hyperplasia. DHM treatment significantly reduced the total number of inflammatory cells, including eosinophils, neutrophils, lymphocytes and macrophages, in the BAL fluid. DHM also reduced the levels of IL-4, IL-5 and IL-13 in the BAL fluid, and reduced the secretion of OVA-specific IgE and IgG1 in the serum. The histological staining demonstrated that DHM treatment effectively suppressed the OVA-induced inflammatory cells in the lung tissues and in the mucus hypersecreted by goblet cells in the airway. These results showed that DHM had a potent anti-inflammatory effect in an OVA-induced mouse model of asthma, offering potential as an anti-inflammatory agent for the treatment of asthma. D.A. Spandidos 2017-06 2017-04-03 /pmc/articles/PMC5436282/ /pubmed/28393183 http://dx.doi.org/10.3892/mmr.2017.6428 Text en Copyright: © Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Xu, Bin
Huang, Shuran
Wang, Caiying
Zhang, Haitao
Fang, Shengcun
Zhang, Yingming
Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
title Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
title_full Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
title_fullStr Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
title_full_unstemmed Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
title_short Anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
title_sort anti-inflammatory effects of dihydromyricetin in a mouse model of asthma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436282/
https://www.ncbi.nlm.nih.gov/pubmed/28393183
http://dx.doi.org/10.3892/mmr.2017.6428
work_keys_str_mv AT xubin antiinflammatoryeffectsofdihydromyricetininamousemodelofasthma
AT huangshuran antiinflammatoryeffectsofdihydromyricetininamousemodelofasthma
AT wangcaiying antiinflammatoryeffectsofdihydromyricetininamousemodelofasthma
AT zhanghaitao antiinflammatoryeffectsofdihydromyricetininamousemodelofasthma
AT fangshengcun antiinflammatoryeffectsofdihydromyricetininamousemodelofasthma
AT zhangyingming antiinflammatoryeffectsofdihydromyricetininamousemodelofasthma