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Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated

BACKGROUND: Mechanisms behind asthmatic cough are largely unknown. It is known that hyperosmolar challenges provoke cough in asthmatic but not in the healthy subjects. It has been postulated that isocapnic hyperpnea of dry air (IHDA) and hypertonic aerosols act via similar mechanisms in asthma to ca...

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Autores principales: Purokivi, Minna, Koskela, Heikki, Brannan, John D, Kontra, Kirsi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205007/
https://www.ncbi.nlm.nih.gov/pubmed/21999754
http://dx.doi.org/10.1186/1745-9974-7-8
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author Purokivi, Minna
Koskela, Heikki
Brannan, John D
Kontra, Kirsi
author_facet Purokivi, Minna
Koskela, Heikki
Brannan, John D
Kontra, Kirsi
author_sort Purokivi, Minna
collection PubMed
description BACKGROUND: Mechanisms behind asthmatic cough are largely unknown. It is known that hyperosmolar challenges provoke cough in asthmatic but not in the healthy subjects. It has been postulated that isocapnic hyperpnea of dry air (IHDA) and hypertonic aerosols act via similar mechanisms in asthma to cause bronchoconstriction. We investigated whether there is an association between cough response induced by IHDA and hypertonic saline (HS) challenges. METHODS: Thirty-six asthmatic and 14 healthy subjects inhaled HS solutions with increasing osmolalities administered via ultrasonic nebuliser until 15 cumulative coughs were recorded. The IHDA consisted of three three-minute ventilation steps: 30%, 60% and 100% of maximal voluntary ventilation with an end-point of 30 cumulative coughs. The challenges were performed on separate days at least 48 hours between them and within one week. Inhaled salbutamol (400 mcg) was administered before the challenges to prevent bronchoconstriction. The cough response was expressed as the cough-to-dose ratio (CDR) which is the total number of coughs divided by the maximal osmolality inhaled or the maximal ventilation achieved. RESULTS: Cough response to IHDA correlated with the HS challenge (Rs = 0.59, p < 0.001). Cough response to IHDA was at its strongest during the first minute after the challenge. IHDA induced more cough among asthmatic than healthy subjects CDR being (mean ± SD) 0.464 ± 0.514 and 0.011 ± 0.024 coughs/MVV%, p < 0.001, respectively. Salbutamol effectively prevented bronchoconstriction to both challenges. CONCLUSIONS: Asthmatic patients are hypersensitive to the cough-provoking effect of hyperpnoea, as they are to hypertonicity. Cough response induced by IHDA and HS correlated well suggesting similar mechanisms behind the responses.
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spelling pubmed-32050072011-11-01 Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated Purokivi, Minna Koskela, Heikki Brannan, John D Kontra, Kirsi Cough Research BACKGROUND: Mechanisms behind asthmatic cough are largely unknown. It is known that hyperosmolar challenges provoke cough in asthmatic but not in the healthy subjects. It has been postulated that isocapnic hyperpnea of dry air (IHDA) and hypertonic aerosols act via similar mechanisms in asthma to cause bronchoconstriction. We investigated whether there is an association between cough response induced by IHDA and hypertonic saline (HS) challenges. METHODS: Thirty-six asthmatic and 14 healthy subjects inhaled HS solutions with increasing osmolalities administered via ultrasonic nebuliser until 15 cumulative coughs were recorded. The IHDA consisted of three three-minute ventilation steps: 30%, 60% and 100% of maximal voluntary ventilation with an end-point of 30 cumulative coughs. The challenges were performed on separate days at least 48 hours between them and within one week. Inhaled salbutamol (400 mcg) was administered before the challenges to prevent bronchoconstriction. The cough response was expressed as the cough-to-dose ratio (CDR) which is the total number of coughs divided by the maximal osmolality inhaled or the maximal ventilation achieved. RESULTS: Cough response to IHDA correlated with the HS challenge (Rs = 0.59, p < 0.001). Cough response to IHDA was at its strongest during the first minute after the challenge. IHDA induced more cough among asthmatic than healthy subjects CDR being (mean ± SD) 0.464 ± 0.514 and 0.011 ± 0.024 coughs/MVV%, p < 0.001, respectively. Salbutamol effectively prevented bronchoconstriction to both challenges. CONCLUSIONS: Asthmatic patients are hypersensitive to the cough-provoking effect of hyperpnoea, as they are to hypertonicity. Cough response induced by IHDA and HS correlated well suggesting similar mechanisms behind the responses. BioMed Central 2011-10-14 /pmc/articles/PMC3205007/ /pubmed/21999754 http://dx.doi.org/10.1186/1745-9974-7-8 Text en Copyright ©2011 Purokivi 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 cited.
spellingShingle Research
Purokivi, Minna
Koskela, Heikki
Brannan, John D
Kontra, Kirsi
Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
title Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
title_full Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
title_fullStr Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
title_full_unstemmed Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
title_short Cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
title_sort cough response to isocapnic hyperpnoea of dry air and hypertonic saline are interrelated
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205007/
https://www.ncbi.nlm.nih.gov/pubmed/21999754
http://dx.doi.org/10.1186/1745-9974-7-8
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