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Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels

BACKGROUND: Cough, the most important airways defensive mechanism is modulated by many afferent inputs either from respiratory tussigenic areas, but also by afferent drive from other organs. In animal models, modulation of cough by nasal afferent inputs can either facilitate or inhibit the cough res...

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Autores principales: Buday, Tomas, Brozmanova, Mariana, Biringerova, Zuzana, Gavliakova, Silvia, Poliacek, Ivan, Calkovsky, Vladimir, Shetthalli, Manjunath V, Plevkova, Jana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546011/
https://www.ncbi.nlm.nih.gov/pubmed/23199233
http://dx.doi.org/10.1186/1745-9974-8-11
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author Buday, Tomas
Brozmanova, Mariana
Biringerova, Zuzana
Gavliakova, Silvia
Poliacek, Ivan
Calkovsky, Vladimir
Shetthalli, Manjunath V
Plevkova, Jana
author_facet Buday, Tomas
Brozmanova, Mariana
Biringerova, Zuzana
Gavliakova, Silvia
Poliacek, Ivan
Calkovsky, Vladimir
Shetthalli, Manjunath V
Plevkova, Jana
author_sort Buday, Tomas
collection PubMed
description BACKGROUND: Cough, the most important airways defensive mechanism is modulated by many afferent inputs either from respiratory tussigenic areas, but also by afferent drive from other organs. In animal models, modulation of cough by nasal afferent inputs can either facilitate or inhibit the cough response, depending on the type of trigeminal afferents stimulated. METHODS: In this study we addressed the question of possible bidirectional modulation of cough response in human healthy volunteers by nasal challenges with TRPA1 and TRPM8 agonists respectively. After nasal challenges with isocyanate (AITC), cinnamaldehyde, (−) menthol and (+) menthol (all 10(-3) M) nasal symptom score, cough threshold (C2), urge to cough (Cu) and cumulative cough response were measured). RESULTS: Nasal challenges with TRPA1 relevant agonists induced considerable nasal symptoms, significantly enhanced urge to cough (p<0.05) but no statistically significant modulation of the C2 and cumulative cough response. In contrast, both TRPM8 agonists administered to the nose significantly modulated all parameters including C2 (p<0.05), Cu (p<0.01) and cumulative cough response (p <0.01) documenting strong anti irritating potential of menthol isomers. CONCLUSIONS: In addition to trigeminal afferents expressing TRP channels, olfactory nerve endings, trigemino – olfactoric relationships, the smell perception process and other supramedullar influences should be considered as potential modulators of the cough response in humans.
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spelling pubmed-35460112013-01-17 Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels Buday, Tomas Brozmanova, Mariana Biringerova, Zuzana Gavliakova, Silvia Poliacek, Ivan Calkovsky, Vladimir Shetthalli, Manjunath V Plevkova, Jana Cough Research BACKGROUND: Cough, the most important airways defensive mechanism is modulated by many afferent inputs either from respiratory tussigenic areas, but also by afferent drive from other organs. In animal models, modulation of cough by nasal afferent inputs can either facilitate or inhibit the cough response, depending on the type of trigeminal afferents stimulated. METHODS: In this study we addressed the question of possible bidirectional modulation of cough response in human healthy volunteers by nasal challenges with TRPA1 and TRPM8 agonists respectively. After nasal challenges with isocyanate (AITC), cinnamaldehyde, (−) menthol and (+) menthol (all 10(-3) M) nasal symptom score, cough threshold (C2), urge to cough (Cu) and cumulative cough response were measured). RESULTS: Nasal challenges with TRPA1 relevant agonists induced considerable nasal symptoms, significantly enhanced urge to cough (p<0.05) but no statistically significant modulation of the C2 and cumulative cough response. In contrast, both TRPM8 agonists administered to the nose significantly modulated all parameters including C2 (p<0.05), Cu (p<0.01) and cumulative cough response (p <0.01) documenting strong anti irritating potential of menthol isomers. CONCLUSIONS: In addition to trigeminal afferents expressing TRP channels, olfactory nerve endings, trigemino – olfactoric relationships, the smell perception process and other supramedullar influences should be considered as potential modulators of the cough response in humans. BioMed Central 2012-12-03 /pmc/articles/PMC3546011/ /pubmed/23199233 http://dx.doi.org/10.1186/1745-9974-8-11 Text en Copyright ©2012 Buday 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
Buday, Tomas
Brozmanova, Mariana
Biringerova, Zuzana
Gavliakova, Silvia
Poliacek, Ivan
Calkovsky, Vladimir
Shetthalli, Manjunath V
Plevkova, Jana
Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels
title Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels
title_full Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels
title_fullStr Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels
title_full_unstemmed Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels
title_short Modulation of cough response by sensory inputs from the nose - role of trigeminal TRPA1 versus TRPM8 channels
title_sort modulation of cough response by sensory inputs from the nose - role of trigeminal trpa1 versus trpm8 channels
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546011/
https://www.ncbi.nlm.nih.gov/pubmed/23199233
http://dx.doi.org/10.1186/1745-9974-8-11
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