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Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation

BACKGROUND: Previously, we showed that treatment with the Rho-kinase inhibitor Y-27632 was able to control airway responsiveness, inflammation, remodeling, and oxidative stress in an animal model of asthma, suggesting that this drug is beneficial in asthma. However, studies evaluating the effects of...

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Autores principales: Pigati, Patricia Angeli, Righetti, Renato Fraga, Possa, Samantha Souza, Romanholo, Beatriz Saraiva, Rodrigues, Adriana Palmeira Dias, dos Santos, Anelize Sartori Alves, Xisto, Débora Gonçalves, Antunes, Mariana Alves, Prado, Carla Máximo, Leick, Edna Aparecida, de Arruda Martins, Milton, Rocco, Patrícia Rieken Macedo, de Fátima Lopes Calvo Tibério, Iolanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531528/
https://www.ncbi.nlm.nih.gov/pubmed/26264367
http://dx.doi.org/10.1186/s12890-015-0073-4
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author Pigati, Patricia Angeli
Righetti, Renato Fraga
Possa, Samantha Souza
Romanholo, Beatriz Saraiva
Rodrigues, Adriana Palmeira Dias
dos Santos, Anelize Sartori Alves
Xisto, Débora Gonçalves
Antunes, Mariana Alves
Prado, Carla Máximo
Leick, Edna Aparecida
de Arruda Martins, Milton
Rocco, Patrícia Rieken Macedo
de Fátima Lopes Calvo Tibério, Iolanda
author_facet Pigati, Patricia Angeli
Righetti, Renato Fraga
Possa, Samantha Souza
Romanholo, Beatriz Saraiva
Rodrigues, Adriana Palmeira Dias
dos Santos, Anelize Sartori Alves
Xisto, Débora Gonçalves
Antunes, Mariana Alves
Prado, Carla Máximo
Leick, Edna Aparecida
de Arruda Martins, Milton
Rocco, Patrícia Rieken Macedo
de Fátima Lopes Calvo Tibério, Iolanda
author_sort Pigati, Patricia Angeli
collection PubMed
description BACKGROUND: Previously, we showed that treatment with the Rho-kinase inhibitor Y-27632 was able to control airway responsiveness, inflammation, remodeling, and oxidative stress in an animal model of asthma, suggesting that this drug is beneficial in asthma. However, studies evaluating the effects of these inhibitors in conjunction with corticosteroids on chronic pulmonary inflammation have not been conducted. Therefore, we evaluated the effects of treatment with the Rho-kinase inhibitor Y-27632, with or without concurrent dexamethasone treatment, on airway and lung tissue mechanical responses, inflammation, extracellular matrix remodeling, and oxidative stress in guinea pigs with chronic allergic inflammation. METHODS: The guinea pigs were subjected to seven ovalbumin or saline inhalation exposures. Treatment with Y-27632 (1 mM) and dexamethasone (2 mg/kg) started at the fifth inhalation. Seventy-two hours after the seventh inhalation, the pulmonary mechanics were evaluated and exhaled nitric oxide (E(NO)) levels were determined. The lungs were removed and histological analysis was performed using morphometry. RESULTS: The treatment of guinea pigs with the Rho-kinase inhibitor and dexamethasone (ORC group) decreased E(NO), the maximal mechanical responses after antigen challenge, inflammation, extracellular matrix remodeling and oxidative stress in the lungs. This therapeutic strategy reduced the levels of collagen and IFN-γ in the airway walls, as well as IL-2, IFN-γ, 8-iso-PGF2α and NF-κB in the distal parenchyma, when compared to isolated treatment with corticosteroid or Rho-kinase inhibitor (P < 0.05) and reduced the number of TIMP-1-positive cells and eosinophils in the alveolar septa compared to corticosteroid-treated animals (P < 0.05). The combined treatment with the Rho-kinase inhibitor and the corticosteroid provided maximal control over the remodeling response and inflammation in the airways and parenchyma. CONCLUSIONS: Rho-kinase inhibition, alone or in combination with corticosteroids, can be considered a future pharmacological tool for the control of asthma.
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spelling pubmed-45315282015-08-12 Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation Pigati, Patricia Angeli Righetti, Renato Fraga Possa, Samantha Souza Romanholo, Beatriz Saraiva Rodrigues, Adriana Palmeira Dias dos Santos, Anelize Sartori Alves Xisto, Débora Gonçalves Antunes, Mariana Alves Prado, Carla Máximo Leick, Edna Aparecida de Arruda Martins, Milton Rocco, Patrícia Rieken Macedo de Fátima Lopes Calvo Tibério, Iolanda BMC Pulm Med Research Article BACKGROUND: Previously, we showed that treatment with the Rho-kinase inhibitor Y-27632 was able to control airway responsiveness, inflammation, remodeling, and oxidative stress in an animal model of asthma, suggesting that this drug is beneficial in asthma. However, studies evaluating the effects of these inhibitors in conjunction with corticosteroids on chronic pulmonary inflammation have not been conducted. Therefore, we evaluated the effects of treatment with the Rho-kinase inhibitor Y-27632, with or without concurrent dexamethasone treatment, on airway and lung tissue mechanical responses, inflammation, extracellular matrix remodeling, and oxidative stress in guinea pigs with chronic allergic inflammation. METHODS: The guinea pigs were subjected to seven ovalbumin or saline inhalation exposures. Treatment with Y-27632 (1 mM) and dexamethasone (2 mg/kg) started at the fifth inhalation. Seventy-two hours after the seventh inhalation, the pulmonary mechanics were evaluated and exhaled nitric oxide (E(NO)) levels were determined. The lungs were removed and histological analysis was performed using morphometry. RESULTS: The treatment of guinea pigs with the Rho-kinase inhibitor and dexamethasone (ORC group) decreased E(NO), the maximal mechanical responses after antigen challenge, inflammation, extracellular matrix remodeling and oxidative stress in the lungs. This therapeutic strategy reduced the levels of collagen and IFN-γ in the airway walls, as well as IL-2, IFN-γ, 8-iso-PGF2α and NF-κB in the distal parenchyma, when compared to isolated treatment with corticosteroid or Rho-kinase inhibitor (P < 0.05) and reduced the number of TIMP-1-positive cells and eosinophils in the alveolar septa compared to corticosteroid-treated animals (P < 0.05). The combined treatment with the Rho-kinase inhibitor and the corticosteroid provided maximal control over the remodeling response and inflammation in the airways and parenchyma. CONCLUSIONS: Rho-kinase inhibition, alone or in combination with corticosteroids, can be considered a future pharmacological tool for the control of asthma. BioMed Central 2015-08-12 /pmc/articles/PMC4531528/ /pubmed/26264367 http://dx.doi.org/10.1186/s12890-015-0073-4 Text en © Pigati et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Pigati, Patricia Angeli
Righetti, Renato Fraga
Possa, Samantha Souza
Romanholo, Beatriz Saraiva
Rodrigues, Adriana Palmeira Dias
dos Santos, Anelize Sartori Alves
Xisto, Débora Gonçalves
Antunes, Mariana Alves
Prado, Carla Máximo
Leick, Edna Aparecida
de Arruda Martins, Milton
Rocco, Patrícia Rieken Macedo
de Fátima Lopes Calvo Tibério, Iolanda
Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
title Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
title_full Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
title_fullStr Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
title_full_unstemmed Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
title_short Y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
title_sort y-27632 is associated with corticosteroid-potentiated control of pulmonary remodeling and inflammation in guinea pigs with chronic allergic inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531528/
https://www.ncbi.nlm.nih.gov/pubmed/26264367
http://dx.doi.org/10.1186/s12890-015-0073-4
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