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Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs
Cough remains a major unmet clinical need, and preclinical animal models are not predictive for new antitussive agents. We have investigated the mechanisms and pharmacological sensitivity of ozone-induced hypertussive responses in rabbits and guinea pigs. Ozone induced a significant increase in coug...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Pharmacology and Experimental Therapeutics
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977573/ https://www.ncbi.nlm.nih.gov/pubmed/26837703 http://dx.doi.org/10.1124/jpet.115.230227 |
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author | Clay, Emlyn Patacchini, Riccardo Trevisani, Marcello Preti, Delia Branà, Maria Pia Spina, Domenico Page, Clive |
author_facet | Clay, Emlyn Patacchini, Riccardo Trevisani, Marcello Preti, Delia Branà, Maria Pia Spina, Domenico Page, Clive |
author_sort | Clay, Emlyn |
collection | PubMed |
description | Cough remains a major unmet clinical need, and preclinical animal models are not predictive for new antitussive agents. We have investigated the mechanisms and pharmacological sensitivity of ozone-induced hypertussive responses in rabbits and guinea pigs. Ozone induced a significant increase in cough frequency and a decrease in time to first cough to inhaled citric acid in both conscious guinea pigs and rabbits. This response was inhibited by the established antitussive drugs codeine and levodropropizine. In contrast to the guinea pig, hypertussive responses in the rabbit were not inhibited by bronchodilator drugs (β(2) agonists or muscarinic receptor antagonists), suggesting that the observed hypertussive state was not secondary to bronchoconstriction in this species. The ozone-induced hypertussive response in the rabbit was inhibited by chronic pretreatment with capsaicin, suggestive of a sensitization of airway sensory nerve fibers. However, we could find no evidence for a role of TRPA1 in this response, suggesting that ozone was not sensitizing airway sensory nerves via activation of this receptor. Whereas the ozone-induced hypertussive response was accompanied by a significant influx of neutrophils into the airway, the hypertussive response was not inhibited by the anti-inflammatory phosphodiesterase 4 inhibitor roflumilast at a dose that clearly exhibited anti-inflammatory activity. In summary, our results suggest that ozone-induced hypertussive responses to citric acid may provide a useful model for the investigation of novel drugs for the treatment of cough, but some important differences were noted between the two species with respect to sensitivity to bronchodilator drugs. |
format | Online Article Text |
id | pubmed-4977573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The American Society for Pharmacology and Experimental Therapeutics |
record_format | MEDLINE/PubMed |
spelling | pubmed-49775732016-08-17 Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs Clay, Emlyn Patacchini, Riccardo Trevisani, Marcello Preti, Delia Branà, Maria Pia Spina, Domenico Page, Clive J Pharmacol Exp Ther Gastrointestinal, Hepatic, Pulmonary, and Renal Cough remains a major unmet clinical need, and preclinical animal models are not predictive for new antitussive agents. We have investigated the mechanisms and pharmacological sensitivity of ozone-induced hypertussive responses in rabbits and guinea pigs. Ozone induced a significant increase in cough frequency and a decrease in time to first cough to inhaled citric acid in both conscious guinea pigs and rabbits. This response was inhibited by the established antitussive drugs codeine and levodropropizine. In contrast to the guinea pig, hypertussive responses in the rabbit were not inhibited by bronchodilator drugs (β(2) agonists or muscarinic receptor antagonists), suggesting that the observed hypertussive state was not secondary to bronchoconstriction in this species. The ozone-induced hypertussive response in the rabbit was inhibited by chronic pretreatment with capsaicin, suggestive of a sensitization of airway sensory nerve fibers. However, we could find no evidence for a role of TRPA1 in this response, suggesting that ozone was not sensitizing airway sensory nerves via activation of this receptor. Whereas the ozone-induced hypertussive response was accompanied by a significant influx of neutrophils into the airway, the hypertussive response was not inhibited by the anti-inflammatory phosphodiesterase 4 inhibitor roflumilast at a dose that clearly exhibited anti-inflammatory activity. In summary, our results suggest that ozone-induced hypertussive responses to citric acid may provide a useful model for the investigation of novel drugs for the treatment of cough, but some important differences were noted between the two species with respect to sensitivity to bronchodilator drugs. The American Society for Pharmacology and Experimental Therapeutics 2016-04 2016-04 /pmc/articles/PMC4977573/ /pubmed/26837703 http://dx.doi.org/10.1124/jpet.115.230227 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the CC BY Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Gastrointestinal, Hepatic, Pulmonary, and Renal Clay, Emlyn Patacchini, Riccardo Trevisani, Marcello Preti, Delia Branà, Maria Pia Spina, Domenico Page, Clive Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs |
title | Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs |
title_full | Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs |
title_fullStr | Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs |
title_full_unstemmed | Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs |
title_short | Ozone-Induced Hypertussive Responses in Rabbits and Guinea Pigs |
title_sort | ozone-induced hypertussive responses in rabbits and guinea pigs |
topic | Gastrointestinal, Hepatic, Pulmonary, and Renal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977573/ https://www.ncbi.nlm.nih.gov/pubmed/26837703 http://dx.doi.org/10.1124/jpet.115.230227 |
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