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Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD

BACKGROUND: Exposure in a pig barn induces airway inflammation that has similarities with the response observed in acute exacerbations in COPD. METHODS: A total of 15 smokers with COPD and 15 healthy non-smokers were exposed for 2 hours in a pig barn (in vivo exposure). Symptoms were assessed, lung...

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Autores principales: Palmberg, Lena, Sundblad, Britt-Marie, Ji, Jie, Karén, Jakob, Larsson, Kjell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219273/
https://www.ncbi.nlm.nih.gov/pubmed/30464444
http://dx.doi.org/10.2147/COPD.S171495
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author Palmberg, Lena
Sundblad, Britt-Marie
Ji, Jie
Karén, Jakob
Larsson, Kjell
author_facet Palmberg, Lena
Sundblad, Britt-Marie
Ji, Jie
Karén, Jakob
Larsson, Kjell
author_sort Palmberg, Lena
collection PubMed
description BACKGROUND: Exposure in a pig barn induces airway inflammation that has similarities with the response observed in acute exacerbations in COPD. METHODS: A total of 15 smokers with COPD and 15 healthy non-smokers were exposed for 2 hours in a pig barn (in vivo exposure). Symptoms were assessed, lung function measured, and blood and sputum samples taken before and after exposure. Blood neutrophils were isolated and stimulated ex vivo with dust from a pig barn and acetylcholine, and inflammatory markers were analyzed. RESULTS: In vivo exposure caused more symptoms and greater lung function fall in COPD patients than in controls. Baseline concentrations of MMP9, TIMP1, IL6, CXCL8, in sputum and neutrophil blood count were higher in COPD patients than in controls. In vivo exposure increased MMP9, TIMP1, IL6, CXCL8, TNFα, and LTB(4) in sputum and MMP9 and IL6 in blood, with no difference between the groups, and serum CRP increased more in COPD subjects. Expression of choline acetyltransferase and acetylcholinesterase on sputum and blood cells was similar in the groups and uninfluenced by in vivo exposure. Dust exposure ex vivo increased choline acetyltransferase expression in neutrophils, but the dust and acetylcholine response did not differ between the groups before and after in vivo exposure. CONCLUSION: COPD patients exposed in a pig barn experience symptoms similar to those in acute exacerbations and lung function deterioration that is unrelated to bronchial responsiveness. Cholinergic mechanisms are involved in the inflammatory response to dust, with no difference between COPD and non-smokers.
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spelling pubmed-62192732018-11-21 Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD Palmberg, Lena Sundblad, Britt-Marie Ji, Jie Karén, Jakob Larsson, Kjell Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Exposure in a pig barn induces airway inflammation that has similarities with the response observed in acute exacerbations in COPD. METHODS: A total of 15 smokers with COPD and 15 healthy non-smokers were exposed for 2 hours in a pig barn (in vivo exposure). Symptoms were assessed, lung function measured, and blood and sputum samples taken before and after exposure. Blood neutrophils were isolated and stimulated ex vivo with dust from a pig barn and acetylcholine, and inflammatory markers were analyzed. RESULTS: In vivo exposure caused more symptoms and greater lung function fall in COPD patients than in controls. Baseline concentrations of MMP9, TIMP1, IL6, CXCL8, in sputum and neutrophil blood count were higher in COPD patients than in controls. In vivo exposure increased MMP9, TIMP1, IL6, CXCL8, TNFα, and LTB(4) in sputum and MMP9 and IL6 in blood, with no difference between the groups, and serum CRP increased more in COPD subjects. Expression of choline acetyltransferase and acetylcholinesterase on sputum and blood cells was similar in the groups and uninfluenced by in vivo exposure. Dust exposure ex vivo increased choline acetyltransferase expression in neutrophils, but the dust and acetylcholine response did not differ between the groups before and after in vivo exposure. CONCLUSION: COPD patients exposed in a pig barn experience symptoms similar to those in acute exacerbations and lung function deterioration that is unrelated to bronchial responsiveness. Cholinergic mechanisms are involved in the inflammatory response to dust, with no difference between COPD and non-smokers. Dove Medical Press 2018-11-01 /pmc/articles/PMC6219273/ /pubmed/30464444 http://dx.doi.org/10.2147/COPD.S171495 Text en © 2018 Palmberg et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Palmberg, Lena
Sundblad, Britt-Marie
Ji, Jie
Karén, Jakob
Larsson, Kjell
Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD
title Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD
title_full Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD
title_fullStr Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD
title_full_unstemmed Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD
title_short Cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with COPD
title_sort cholinergic mechanisms in an organic dust model simulating an acute exacerbation in patients with copd
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219273/
https://www.ncbi.nlm.nih.gov/pubmed/30464444
http://dx.doi.org/10.2147/COPD.S171495
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