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Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation

Ambroxol is used in COPD and asthma to increase mucociliary clearance and regulate surfactant levels, perhaps through anti-oxidant and anti-inflammatory activities. To determine the role and effect of ambroxol in an experimental model of asthma, BALB/c mice were sensitized to ovalbumin (OVA) followe...

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Autores principales: Takeda, Katsuyuki, Miyahara, Nobuaki, Matsubara, Shigeki, Taube, Christian, Kitamura, Kenichi, Hirano, Astushi, Tanimoto, Mitsune, Gelfand, Erwin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917400/
https://www.ncbi.nlm.nih.gov/pubmed/27340385
http://dx.doi.org/10.4110/in.2016.16.3.165
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author Takeda, Katsuyuki
Miyahara, Nobuaki
Matsubara, Shigeki
Taube, Christian
Kitamura, Kenichi
Hirano, Astushi
Tanimoto, Mitsune
Gelfand, Erwin W.
author_facet Takeda, Katsuyuki
Miyahara, Nobuaki
Matsubara, Shigeki
Taube, Christian
Kitamura, Kenichi
Hirano, Astushi
Tanimoto, Mitsune
Gelfand, Erwin W.
author_sort Takeda, Katsuyuki
collection PubMed
description Ambroxol is used in COPD and asthma to increase mucociliary clearance and regulate surfactant levels, perhaps through anti-oxidant and anti-inflammatory activities. To determine the role and effect of ambroxol in an experimental model of asthma, BALB/c mice were sensitized to ovalbumin (OVA) followed by 3 days of challenge. Airway hyperresponsiveness (AHR), lung cell composition and histology, and cytokine and protein carbonyl levels in bronchoalveolar lavage (BAL) fluid were determined. Ambroxol was administered either before the first OVA challenge or was begun after the last allergen challenge. Cytokine production levels from lung mononuclear cells (Lung MNCs) or alveolar macrophages (AM) were also determined. Administration of ambroxol prior to challenge suppressed AHR, airway eosinophilia, goblet cell metaplasia, and reduced inflammation in subepithelial regions. When given after challenge, AHR was suppressed but without effects on eosinophil numbers. Levels of IL-5 and IL-13 in BAL fluid were decreased when the drug was given prior to challenge; when given after challenge, increased levels of IL-10 and IL-12 were detected. Decreased levels of protein carbonyls were detected in BAL fluid following ambroxol treatment after challenge. In vitro, ambroxol increased levels of IL-10, IFN-γ, and IL-12 from Lung MNCs and AM, whereas IL-4, IL-5, and IL-13 production was not altered. Taken together, ambroxol was effective in preventing AHR and airway inflammation through upregulation of Th1 cytokines and protection from oxidative stress in the airways.
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spelling pubmed-49174002016-06-23 Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation Takeda, Katsuyuki Miyahara, Nobuaki Matsubara, Shigeki Taube, Christian Kitamura, Kenichi Hirano, Astushi Tanimoto, Mitsune Gelfand, Erwin W. Immune Netw Original Article Ambroxol is used in COPD and asthma to increase mucociliary clearance and regulate surfactant levels, perhaps through anti-oxidant and anti-inflammatory activities. To determine the role and effect of ambroxol in an experimental model of asthma, BALB/c mice were sensitized to ovalbumin (OVA) followed by 3 days of challenge. Airway hyperresponsiveness (AHR), lung cell composition and histology, and cytokine and protein carbonyl levels in bronchoalveolar lavage (BAL) fluid were determined. Ambroxol was administered either before the first OVA challenge or was begun after the last allergen challenge. Cytokine production levels from lung mononuclear cells (Lung MNCs) or alveolar macrophages (AM) were also determined. Administration of ambroxol prior to challenge suppressed AHR, airway eosinophilia, goblet cell metaplasia, and reduced inflammation in subepithelial regions. When given after challenge, AHR was suppressed but without effects on eosinophil numbers. Levels of IL-5 and IL-13 in BAL fluid were decreased when the drug was given prior to challenge; when given after challenge, increased levels of IL-10 and IL-12 were detected. Decreased levels of protein carbonyls were detected in BAL fluid following ambroxol treatment after challenge. In vitro, ambroxol increased levels of IL-10, IFN-γ, and IL-12 from Lung MNCs and AM, whereas IL-4, IL-5, and IL-13 production was not altered. Taken together, ambroxol was effective in preventing AHR and airway inflammation through upregulation of Th1 cytokines and protection from oxidative stress in the airways. The Korean Association of Immunologists 2016-06 2016-06-17 /pmc/articles/PMC4917400/ /pubmed/27340385 http://dx.doi.org/10.4110/in.2016.16.3.165 Text en Copyright © 2016 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Takeda, Katsuyuki
Miyahara, Nobuaki
Matsubara, Shigeki
Taube, Christian
Kitamura, Kenichi
Hirano, Astushi
Tanimoto, Mitsune
Gelfand, Erwin W.
Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation
title Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation
title_full Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation
title_fullStr Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation
title_full_unstemmed Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation
title_short Immunomodulatory Effects of Ambroxol on Airway Hyperresponsiveness and Inflammation
title_sort immunomodulatory effects of ambroxol on airway hyperresponsiveness and inflammation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917400/
https://www.ncbi.nlm.nih.gov/pubmed/27340385
http://dx.doi.org/10.4110/in.2016.16.3.165
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