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Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent

Erdosteine is a drug approved for the treatment of acute and chronic pulmonary diseases, originally developed as a mucolytic agent. It belongs to the thiol-based family of drugs that are known to also possess potentially important antioxidant and anti-inflammatory properties, and exhibit antibacteri...

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Autores principales: Cazzola, Mario, Page, Clive, Rogliani, Paola, Calzetta, Luigino, Matera, Maria Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647991/
https://www.ncbi.nlm.nih.gov/pubmed/33025535
http://dx.doi.org/10.1007/s40265-020-01412-x
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author Cazzola, Mario
Page, Clive
Rogliani, Paola
Calzetta, Luigino
Matera, Maria Gabriella
author_facet Cazzola, Mario
Page, Clive
Rogliani, Paola
Calzetta, Luigino
Matera, Maria Gabriella
author_sort Cazzola, Mario
collection PubMed
description Erdosteine is a drug approved for the treatment of acute and chronic pulmonary diseases, originally developed as a mucolytic agent. It belongs to the thiol-based family of drugs that are known to also possess potentially important antioxidant and anti-inflammatory properties, and exhibit antibacterial activity against a variety of medically important bacterial species. Erdosteine is a prodrug that is metabolized to the ring-opening compound metabolite M1 (MET 1), which has mucolytic properties. Experimental studies have documented that erdosteine prevents or reduces lung tissue damage induced by oxidative stress and, in particular, that Met 1 also regulates reactive oxygen species production. The RESTORE study, which has been the only trial that investigated the effects of a thiol-based drug in chronic obstructive pulmonary disease (COPD) frequent exacerbators, documented that erdosteine significantly reduces the risk of acute exacerbations of COPD (AECOPDs), shortens their course, and also decreases the risk of hospitalization from COPD. The preventive action of erdosteine on AECOPDs was not affected by the presence or absence of inhaled corticosteroids (ICSs) or blood eosinophil count. These findings clearly contrast with the Global Initiative for Chronic Obstructive Lung Disease strategy’s approach to use erdosteine only in those COPD patients not treated simultaneously with an ICS. Furthermore, they support the possibility of using erdosteine in a step-down approach that in COPD is characterized by the withdrawal of the ICS.
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spelling pubmed-76479912020-11-10 Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent Cazzola, Mario Page, Clive Rogliani, Paola Calzetta, Luigino Matera, Maria Gabriella Drugs Review Article Erdosteine is a drug approved for the treatment of acute and chronic pulmonary diseases, originally developed as a mucolytic agent. It belongs to the thiol-based family of drugs that are known to also possess potentially important antioxidant and anti-inflammatory properties, and exhibit antibacterial activity against a variety of medically important bacterial species. Erdosteine is a prodrug that is metabolized to the ring-opening compound metabolite M1 (MET 1), which has mucolytic properties. Experimental studies have documented that erdosteine prevents or reduces lung tissue damage induced by oxidative stress and, in particular, that Met 1 also regulates reactive oxygen species production. The RESTORE study, which has been the only trial that investigated the effects of a thiol-based drug in chronic obstructive pulmonary disease (COPD) frequent exacerbators, documented that erdosteine significantly reduces the risk of acute exacerbations of COPD (AECOPDs), shortens their course, and also decreases the risk of hospitalization from COPD. The preventive action of erdosteine on AECOPDs was not affected by the presence or absence of inhaled corticosteroids (ICSs) or blood eosinophil count. These findings clearly contrast with the Global Initiative for Chronic Obstructive Lung Disease strategy’s approach to use erdosteine only in those COPD patients not treated simultaneously with an ICS. Furthermore, they support the possibility of using erdosteine in a step-down approach that in COPD is characterized by the withdrawal of the ICS. Springer International Publishing 2020-10-06 2020 /pmc/articles/PMC7647991/ /pubmed/33025535 http://dx.doi.org/10.1007/s40265-020-01412-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review Article
Cazzola, Mario
Page, Clive
Rogliani, Paola
Calzetta, Luigino
Matera, Maria Gabriella
Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent
title Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent
title_full Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent
title_fullStr Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent
title_full_unstemmed Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent
title_short Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent
title_sort multifaceted beneficial effects of erdosteine: more than a mucolytic agent
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647991/
https://www.ncbi.nlm.nih.gov/pubmed/33025535
http://dx.doi.org/10.1007/s40265-020-01412-x
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