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Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model

Proton pump inhibitors (PPIs) are well-known antacid drugs developed to treat gastric disorders. Emerging studies demonstrate that PPIs possess biological activities that extend beyond inhibition of H(+)/K(+) ATPase (proton pumps) expressed in parietal cells of the stomach. Some of the extra-gastric...

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Autores principales: Nelson, Christina, Lee, Jameisha, Ko, Kang, Sikora, Andrew G., Bonnen, Mark D., Enkhbaatar, Perenlei, Ghebre, Yohannes T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266706/
https://www.ncbi.nlm.nih.gov/pubmed/28184197
http://dx.doi.org/10.3389/fphar.2017.00016
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author Nelson, Christina
Lee, Jameisha
Ko, Kang
Sikora, Andrew G.
Bonnen, Mark D.
Enkhbaatar, Perenlei
Ghebre, Yohannes T.
author_facet Nelson, Christina
Lee, Jameisha
Ko, Kang
Sikora, Andrew G.
Bonnen, Mark D.
Enkhbaatar, Perenlei
Ghebre, Yohannes T.
author_sort Nelson, Christina
collection PubMed
description Proton pump inhibitors (PPIs) are well-known antacid drugs developed to treat gastric disorders. Emerging studies demonstrate that PPIs possess biological activities that extend beyond inhibition of H(+)/K(+) ATPase (proton pumps) expressed in parietal cells of the stomach. Some of the extra-gastric activities of PPIs include modulation of epithelial, endothelial, and immune cell functions. Recently, we reported that PPIs suppress the expression of several proinflammatory and profibrotic molecules, as well as enhance antioxidant mechanisms in order to favorably regulate lung inflammation and fibrosis in an animal model of bleomycin-induced lung injury. In addition, several retrospective clinical studies report that the use of PPIs is associated with beneficial outcomes in chronic lung diseases including idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD). Based on these preclinical and clinical observations, we hypothesized that PPIs ameliorate smoke-induced lung injury. Accordingly, we evaluated the pharmacological efficacy of the PPI esomeprazole in a mouse model of cotton smoke-induced lung injury. The animals were exposed to cotton smoke for 3-weeks in the presence or absence of esomeprazole treatment. We found that therapeutic administration of esomeprazole significantly inhibited the progression of fibrosis throughout the lungs of the animals in this group compared to controls. In addition, esomeprazole also reduced circulating markers of inflammation and fibrosis. Overall, our work extends the emerging anti-inflammatory and antifibrotic potential of PPIs and their role in modulation of chronic lung diseases.
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spelling pubmed-52667062017-02-09 Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model Nelson, Christina Lee, Jameisha Ko, Kang Sikora, Andrew G. Bonnen, Mark D. Enkhbaatar, Perenlei Ghebre, Yohannes T. Front Pharmacol Pharmacology Proton pump inhibitors (PPIs) are well-known antacid drugs developed to treat gastric disorders. Emerging studies demonstrate that PPIs possess biological activities that extend beyond inhibition of H(+)/K(+) ATPase (proton pumps) expressed in parietal cells of the stomach. Some of the extra-gastric activities of PPIs include modulation of epithelial, endothelial, and immune cell functions. Recently, we reported that PPIs suppress the expression of several proinflammatory and profibrotic molecules, as well as enhance antioxidant mechanisms in order to favorably regulate lung inflammation and fibrosis in an animal model of bleomycin-induced lung injury. In addition, several retrospective clinical studies report that the use of PPIs is associated with beneficial outcomes in chronic lung diseases including idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD). Based on these preclinical and clinical observations, we hypothesized that PPIs ameliorate smoke-induced lung injury. Accordingly, we evaluated the pharmacological efficacy of the PPI esomeprazole in a mouse model of cotton smoke-induced lung injury. The animals were exposed to cotton smoke for 3-weeks in the presence or absence of esomeprazole treatment. We found that therapeutic administration of esomeprazole significantly inhibited the progression of fibrosis throughout the lungs of the animals in this group compared to controls. In addition, esomeprazole also reduced circulating markers of inflammation and fibrosis. Overall, our work extends the emerging anti-inflammatory and antifibrotic potential of PPIs and their role in modulation of chronic lung diseases. Frontiers Media S.A. 2017-01-26 /pmc/articles/PMC5266706/ /pubmed/28184197 http://dx.doi.org/10.3389/fphar.2017.00016 Text en Copyright © 2017 Nelson, Lee, Ko, Sikora, Bonnen, Enkhbaatar and Ghebre. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Nelson, Christina
Lee, Jameisha
Ko, Kang
Sikora, Andrew G.
Bonnen, Mark D.
Enkhbaatar, Perenlei
Ghebre, Yohannes T.
Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model
title Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model
title_full Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model
title_fullStr Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model
title_full_unstemmed Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model
title_short Therapeutic Efficacy of Esomeprazole in Cotton Smoke-Induced Lung Injury Model
title_sort therapeutic efficacy of esomeprazole in cotton smoke-induced lung injury model
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266706/
https://www.ncbi.nlm.nih.gov/pubmed/28184197
http://dx.doi.org/10.3389/fphar.2017.00016
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