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Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease

Chronic obstructive pulmonary disease (COPD) is among the leading causes of morbidity and mortality worldwide. Glucocorticoids are currently the most applicable anti-inflammatory treatment for COPD. However, a subset of COPD subjects is relatively insensitive to this treatment. Fenspiride, a non-cor...

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Autores principales: Kuzubova, Nataliya A., Lebedeva, Elena S., Fedin, Anatoliy N., Dvorakovskaya, Ivetta V., Preobrazhenskaya, Tatiana N., Titova, Olga N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Society of Smooth Muscle Research 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137255/
https://www.ncbi.nlm.nih.gov/pubmed/24133694
http://dx.doi.org/10.1540/jsmr.49.46
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author Kuzubova, Nataliya A.
Lebedeva, Elena S.
Fedin, Anatoliy N.
Dvorakovskaya, Ivetta V.
Preobrazhenskaya, Tatiana N.
Titova, Olga N.
author_facet Kuzubova, Nataliya A.
Lebedeva, Elena S.
Fedin, Anatoliy N.
Dvorakovskaya, Ivetta V.
Preobrazhenskaya, Tatiana N.
Titova, Olga N.
author_sort Kuzubova, Nataliya A.
collection PubMed
description Chronic obstructive pulmonary disease (COPD) is among the leading causes of morbidity and mortality worldwide. Glucocorticoids are currently the most applicable anti-inflammatory treatment for COPD. However, a subset of COPD subjects is relatively insensitive to this treatment. Fenspiride, a non-corticosteroid anti-inflammatory drug, has been described to have beneficial effects in patients with COPD, although the mechanism of its action is not well known. The effect of fenspiride on contractile activity of bronchial smooth muscle was studied in a rat model of COPD induced by long-term exposure of the animals to nitrogen dioxide (NO(2)). Contractile activity of bronchial smooth muscle was evaluated in vitro. Isometric contraction of bronchial preparations was measured following electrical stimulation. Fenspiride administration to rats during the acute stage of COPD (15 days of NO(2) exposure) prevented the bronchial constriction induced by NO(2). The bronchodilator effect of a low-dose of fenspiride (0.15 mg/kg) was mediated by interaction with the nerve endings of capsaicin-sensitive C-fibers. Interaction of fenspiride with C-fibers was shown to prevent initiation of neurogenic inflammation, as evidenced by lack of COPD-like structural changes in the lungs. The bronchodilator effect of a high-dose of fenspiride (15 mg/kg) was mediated not only by the afferent component, but also involved a direct relaxing effect on smooth muscle cells. The anti-inflammatory and bronchodilator effects of a low-dose of fenspiride may be used for prevention of COPD development in individuals from high-risk cohorts exposed to aggressive environmental factors.
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spelling pubmed-51372552017-02-14 Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease Kuzubova, Nataliya A. Lebedeva, Elena S. Fedin, Anatoliy N. Dvorakovskaya, Ivetta V. Preobrazhenskaya, Tatiana N. Titova, Olga N. J Smooth Muscle Res Original Chronic obstructive pulmonary disease (COPD) is among the leading causes of morbidity and mortality worldwide. Glucocorticoids are currently the most applicable anti-inflammatory treatment for COPD. However, a subset of COPD subjects is relatively insensitive to this treatment. Fenspiride, a non-corticosteroid anti-inflammatory drug, has been described to have beneficial effects in patients with COPD, although the mechanism of its action is not well known. The effect of fenspiride on contractile activity of bronchial smooth muscle was studied in a rat model of COPD induced by long-term exposure of the animals to nitrogen dioxide (NO(2)). Contractile activity of bronchial smooth muscle was evaluated in vitro. Isometric contraction of bronchial preparations was measured following electrical stimulation. Fenspiride administration to rats during the acute stage of COPD (15 days of NO(2) exposure) prevented the bronchial constriction induced by NO(2). The bronchodilator effect of a low-dose of fenspiride (0.15 mg/kg) was mediated by interaction with the nerve endings of capsaicin-sensitive C-fibers. Interaction of fenspiride with C-fibers was shown to prevent initiation of neurogenic inflammation, as evidenced by lack of COPD-like structural changes in the lungs. The bronchodilator effect of a high-dose of fenspiride (15 mg/kg) was mediated not only by the afferent component, but also involved a direct relaxing effect on smooth muscle cells. The anti-inflammatory and bronchodilator effects of a low-dose of fenspiride may be used for prevention of COPD development in individuals from high-risk cohorts exposed to aggressive environmental factors. Japan Society of Smooth Muscle Research 2013-09-20 2013 /pmc/articles/PMC5137255/ /pubmed/24133694 http://dx.doi.org/10.1540/jsmr.49.46 Text en ©2013 The Japan Society of Smooth Muscle Research http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original
Kuzubova, Nataliya A.
Lebedeva, Elena S.
Fedin, Anatoliy N.
Dvorakovskaya, Ivetta V.
Preobrazhenskaya, Tatiana N.
Titova, Olga N.
Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease
title Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease
title_full Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease
title_fullStr Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease
title_full_unstemmed Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease
title_short Effect of Fenspiride on Bronchial Smooth Muscle of Rats with Chronic Obstructive Pulmonary Disease
title_sort effect of fenspiride on bronchial smooth muscle of rats with chronic obstructive pulmonary disease
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137255/
https://www.ncbi.nlm.nih.gov/pubmed/24133694
http://dx.doi.org/10.1540/jsmr.49.46
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