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Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice

BACKGROUND: Tulobuterol patch, one of strongest bronchodilators, was recently shown to improve bronchial hyperresponsiveness and significantly decrease the sputum eosinophil counts by combining with nonspecific anti-inflammatory drugs on patients with asthma. However, there is limited study on the a...

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Autores principales: Fu, Lixia, Guan, Jing, Zhang, Yujia, Ma, Pei, Zhuang, Yuanyuan, Bai, Jinye, Ding, Yasi, Hou, Qi, Gong, Wan, Lin, Mingbao, Zheng, Wensheng, Zhang, Jianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844735/
https://www.ncbi.nlm.nih.gov/pubmed/29552299
http://dx.doi.org/10.18632/oncotarget.24348
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author Fu, Lixia
Guan, Jing
Zhang, Yujia
Ma, Pei
Zhuang, Yuanyuan
Bai, Jinye
Ding, Yasi
Hou, Qi
Gong, Wan
Lin, Mingbao
Zheng, Wensheng
Zhang, Jianmin
author_facet Fu, Lixia
Guan, Jing
Zhang, Yujia
Ma, Pei
Zhuang, Yuanyuan
Bai, Jinye
Ding, Yasi
Hou, Qi
Gong, Wan
Lin, Mingbao
Zheng, Wensheng
Zhang, Jianmin
author_sort Fu, Lixia
collection PubMed
description BACKGROUND: Tulobuterol patch, one of strongest bronchodilators, was recently shown to improve bronchial hyperresponsiveness and significantly decrease the sputum eosinophil counts by combining with nonspecific anti-inflammatory drugs on patients with asthma. However, there is limited study on the anti-inflammatory activities of tulobuterol patch and its potential machenism. RESULTS: The tulobuterol patch significantly ameliorated inflammatory cell infiltration in the lung tissue, reduced the number of total leukocytes and its differential count, markedly reduced the production of IL-1β, TNF-α, IL-6, CCL-11 and IL-4 in bronchial alveolar lavage fluid, as well as a reduction in IL-4/IFN-γ ratio. Tulobuterol patch exhibited the best effect on allergic inflammation compared with formoterol and salbutamol. Furthermore, tulobuterol patch treatment significantly suppressed the expression and activation of Syk and its downdream signaling NF-κB and p-NF-κB. CONCLUSIONS: The present studies revealed that tulobuterol patch effectively ameliorated airway inflammatory responses in allergic asthma, and its mechanisms, at least partially, via down-regulating Syk/NF-κB pathway. METHODS: An ovalbumin induced allergic asthma mouse model were used, and the effects of tulobuterol patch on allergic airway inflammation were evaluated. Also, its anti-airway inflammatory potential was compared with two other β(2)-agonists, salbutamol and formoterol. Its possible anti-inflammatory mechanisms were identified by using western blotting and immunohistochemistry.
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spelling pubmed-58447352018-03-16 Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice Fu, Lixia Guan, Jing Zhang, Yujia Ma, Pei Zhuang, Yuanyuan Bai, Jinye Ding, Yasi Hou, Qi Gong, Wan Lin, Mingbao Zheng, Wensheng Zhang, Jianmin Oncotarget Research Paper BACKGROUND: Tulobuterol patch, one of strongest bronchodilators, was recently shown to improve bronchial hyperresponsiveness and significantly decrease the sputum eosinophil counts by combining with nonspecific anti-inflammatory drugs on patients with asthma. However, there is limited study on the anti-inflammatory activities of tulobuterol patch and its potential machenism. RESULTS: The tulobuterol patch significantly ameliorated inflammatory cell infiltration in the lung tissue, reduced the number of total leukocytes and its differential count, markedly reduced the production of IL-1β, TNF-α, IL-6, CCL-11 and IL-4 in bronchial alveolar lavage fluid, as well as a reduction in IL-4/IFN-γ ratio. Tulobuterol patch exhibited the best effect on allergic inflammation compared with formoterol and salbutamol. Furthermore, tulobuterol patch treatment significantly suppressed the expression and activation of Syk and its downdream signaling NF-κB and p-NF-κB. CONCLUSIONS: The present studies revealed that tulobuterol patch effectively ameliorated airway inflammatory responses in allergic asthma, and its mechanisms, at least partially, via down-regulating Syk/NF-κB pathway. METHODS: An ovalbumin induced allergic asthma mouse model were used, and the effects of tulobuterol patch on allergic airway inflammation were evaluated. Also, its anti-airway inflammatory potential was compared with two other β(2)-agonists, salbutamol and formoterol. Its possible anti-inflammatory mechanisms were identified by using western blotting and immunohistochemistry. Impact Journals LLC 2018-01-31 /pmc/articles/PMC5844735/ /pubmed/29552299 http://dx.doi.org/10.18632/oncotarget.24348 Text en Copyright: © 2018 Fu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Fu, Lixia
Guan, Jing
Zhang, Yujia
Ma, Pei
Zhuang, Yuanyuan
Bai, Jinye
Ding, Yasi
Hou, Qi
Gong, Wan
Lin, Mingbao
Zheng, Wensheng
Zhang, Jianmin
Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice
title Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice
title_full Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice
title_fullStr Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice
title_full_unstemmed Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice
title_short Tulobuterol patch alleviates allergic asthmic inflammation by blockade of Syk and NF-κB activation in mice
title_sort tulobuterol patch alleviates allergic asthmic inflammation by blockade of syk and nf-κb activation in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844735/
https://www.ncbi.nlm.nih.gov/pubmed/29552299
http://dx.doi.org/10.18632/oncotarget.24348
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