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Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting?
Beta2-adrenoreceptor agonists (β2-agonists) are primarily bronchodilators, targeting airway smooth muscle and providing critical symptomatic relief in conditions such as bronchial asthma and chronic obstructive pulmonary disease. These agents also possess broad-spectrum, secondary, anti-inflammatory...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840775/ https://www.ncbi.nlm.nih.gov/pubmed/24285920 http://dx.doi.org/10.2147/DDDT.S50995 |
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author | Theron, Annette J Steel, Helen C Tintinger, Gregory R Feldman, Charles Anderson, Ronald |
author_facet | Theron, Annette J Steel, Helen C Tintinger, Gregory R Feldman, Charles Anderson, Ronald |
author_sort | Theron, Annette J |
collection | PubMed |
description | Beta2-adrenoreceptor agonists (β2-agonists) are primarily bronchodilators, targeting airway smooth muscle and providing critical symptomatic relief in conditions such as bronchial asthma and chronic obstructive pulmonary disease. These agents also possess broad-spectrum, secondary, anti-inflammatory properties. These are mediated largely, though not exclusively, via interactions with adenylyl cyclase-coupled β2-adrenoreceptors on a range of immune and inflammatory cells involved in the immunopathogenesis of acute and chronic inflammatory disorders of the airways. The clinical relevance of the anti-inflammatory actions of β2-agonists, although often effective in the experimental setting, remains contentious. The primary objectives of the current review are: firstly, to assess the mechanisms, both molecular and cell-associated, that may limit the anti-inflammatory efficacy of β2-agonists; secondly, to evaluate pharmacological strategies, several of which are recent and innovative, that may overcome these limitations. These are preceded by a consideration of the various types of β2-agonists, their clinical applications, and spectrum of anti-inflammatory activities, particularly those involving adenosine 3′,5′-cyclic adenosine monophosphate-activated protein kinase-mediated clearance of cytosolic calcium, and altered gene expression in immune and inflammatory cells. |
format | Online Article Text |
id | pubmed-3840775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38407752013-11-27 Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? Theron, Annette J Steel, Helen C Tintinger, Gregory R Feldman, Charles Anderson, Ronald Drug Des Devel Ther Review Beta2-adrenoreceptor agonists (β2-agonists) are primarily bronchodilators, targeting airway smooth muscle and providing critical symptomatic relief in conditions such as bronchial asthma and chronic obstructive pulmonary disease. These agents also possess broad-spectrum, secondary, anti-inflammatory properties. These are mediated largely, though not exclusively, via interactions with adenylyl cyclase-coupled β2-adrenoreceptors on a range of immune and inflammatory cells involved in the immunopathogenesis of acute and chronic inflammatory disorders of the airways. The clinical relevance of the anti-inflammatory actions of β2-agonists, although often effective in the experimental setting, remains contentious. The primary objectives of the current review are: firstly, to assess the mechanisms, both molecular and cell-associated, that may limit the anti-inflammatory efficacy of β2-agonists; secondly, to evaluate pharmacological strategies, several of which are recent and innovative, that may overcome these limitations. These are preceded by a consideration of the various types of β2-agonists, their clinical applications, and spectrum of anti-inflammatory activities, particularly those involving adenosine 3′,5′-cyclic adenosine monophosphate-activated protein kinase-mediated clearance of cytosolic calcium, and altered gene expression in immune and inflammatory cells. Dove Medical Press 2013-11-22 /pmc/articles/PMC3840775/ /pubmed/24285920 http://dx.doi.org/10.2147/DDDT.S50995 Text en © 2013 Theron et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Theron, Annette J Steel, Helen C Tintinger, Gregory R Feldman, Charles Anderson, Ronald Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
title | Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
title_full | Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
title_fullStr | Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
title_full_unstemmed | Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
title_short | Can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
title_sort | can the anti-inflammatory activities of β2-agonists be harnessed in the clinical setting? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840775/ https://www.ncbi.nlm.nih.gov/pubmed/24285920 http://dx.doi.org/10.2147/DDDT.S50995 |
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