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The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways

Background: The presented study evaluated the suppositional changes in the airway expression of Nav1.8 and Nav1.7 and their role in the airway defense mechanisms in healthy animals and in an experimental asthma model. Methods: The effects of the blockers inhalation on the reactivity of guinea pig ai...

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Autores principales: Kocmalova, Michaela, Kazimierova, Ivana, Barborikova, Jana, Joskova, Marta, Franova, Sona, Sutovska, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304019/
https://www.ncbi.nlm.nih.gov/pubmed/34357161
http://dx.doi.org/10.3390/membranes11070511
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author Kocmalova, Michaela
Kazimierova, Ivana
Barborikova, Jana
Joskova, Marta
Franova, Sona
Sutovska, Martina
author_facet Kocmalova, Michaela
Kazimierova, Ivana
Barborikova, Jana
Joskova, Marta
Franova, Sona
Sutovska, Martina
author_sort Kocmalova, Michaela
collection PubMed
description Background: The presented study evaluated the suppositional changes in the airway expression of Nav1.8 and Nav1.7 and their role in the airway defense mechanisms in healthy animals and in an experimental asthma model. Methods: The effects of the blockers inhalation on the reactivity of guinea pig airways, number of citric-acid-induced coughs and ciliary beating frequency (CBF) were tested in vivo. Chronic inflammation simulating asthma was induced by repetitive exposure to ovalbumin. The expression of Nav1.7 and Nav1.8 was examined by ELISA. Results: The Nav 1.8 blocker showed complex antitussive and bronchodilatory effects and significantly regulated the CBF in healthy and sensitized animals. The Nav1.7 blockers significantly inhibited coughing and participated in CBF control in the ovalbumin-sensitized animals. The increased expression of the respective ion channels in the sensitized animals corresponded to changes in CBF regulation. The therapeutic potency of the Nav1.8 blocker was evidenced in combinations with classic bronchodilators. Conclusion: The allergic-inflammation-upregulated expression of Nav1.7 and Nav1.8 and corresponding effects of blocker inhalation on airway defense mechanisms, along with the Nav1.8 blocker’s compatibility with classic antiasthmatic drugs, bring novel possibilities for the treatment of various respiratory diseases. However, the influence of the Nav1.8 blocker on CBF requires further investigation.
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spelling pubmed-83040192021-07-25 The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways Kocmalova, Michaela Kazimierova, Ivana Barborikova, Jana Joskova, Marta Franova, Sona Sutovska, Martina Membranes (Basel) Article Background: The presented study evaluated the suppositional changes in the airway expression of Nav1.8 and Nav1.7 and their role in the airway defense mechanisms in healthy animals and in an experimental asthma model. Methods: The effects of the blockers inhalation on the reactivity of guinea pig airways, number of citric-acid-induced coughs and ciliary beating frequency (CBF) were tested in vivo. Chronic inflammation simulating asthma was induced by repetitive exposure to ovalbumin. The expression of Nav1.7 and Nav1.8 was examined by ELISA. Results: The Nav 1.8 blocker showed complex antitussive and bronchodilatory effects and significantly regulated the CBF in healthy and sensitized animals. The Nav1.7 blockers significantly inhibited coughing and participated in CBF control in the ovalbumin-sensitized animals. The increased expression of the respective ion channels in the sensitized animals corresponded to changes in CBF regulation. The therapeutic potency of the Nav1.8 blocker was evidenced in combinations with classic bronchodilators. Conclusion: The allergic-inflammation-upregulated expression of Nav1.7 and Nav1.8 and corresponding effects of blocker inhalation on airway defense mechanisms, along with the Nav1.8 blocker’s compatibility with classic antiasthmatic drugs, bring novel possibilities for the treatment of various respiratory diseases. However, the influence of the Nav1.8 blocker on CBF requires further investigation. MDPI 2021-07-07 /pmc/articles/PMC8304019/ /pubmed/34357161 http://dx.doi.org/10.3390/membranes11070511 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kocmalova, Michaela
Kazimierova, Ivana
Barborikova, Jana
Joskova, Marta
Franova, Sona
Sutovska, Martina
The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways
title The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways
title_full The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways
title_fullStr The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways
title_full_unstemmed The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways
title_short The Changes in Expression of Na(V)1.7 and Na(V)1.8 and the Effects of the Inhalation of Their Blockers in Healthy and Ovalbumin-Sensitized Guinea Pig Airways
title_sort changes in expression of na(v)1.7 and na(v)1.8 and the effects of the inhalation of their blockers in healthy and ovalbumin-sensitized guinea pig airways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304019/
https://www.ncbi.nlm.nih.gov/pubmed/34357161
http://dx.doi.org/10.3390/membranes11070511
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