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Molecular and cellular mechanisms underlying the therapeutic effects of budesonide in asthma - 25/09/16

Doi : 10.1016/j.pupt.2016.07.001 
Girolamo Pelaia a, , Alessandro Vatrella b, Maria Teresa Busceti a, Francesco Fabiano c, Rosa Terracciano d, Maria Gabriella Matera e, Rosario Maselli a
a Department of Medical and Surgical Sciences, Section of Respiratory Diseases, University “Magna Græcia” of Catanzaro, Italy 
b Department of Medicine and Surgery, Section of Respiratory Diseases, University of Salerno, Italy 
c Pulmonary Rehabilitation, “Fondazione Don Carlo Gnocchi”, Milan, Italy 
d Department of Health Science, University “Magna Græcia” of Catanzaro, Italy 
e Department of Experimental Medicine, Unit of Pharmacology, Second University of Naples, Italy 

Corresponding author. FCCP Campus Universitario “S. Venuta”, Viale Europa – Località Germaneto, 88100, Catanzaro, Italy.FCCP Campus Universitario “S. Venuta”Viale Europa – Località GermanetoCatanzaro88100Italy

Abstract

Inhaled glucocorticoids are the mainstay of asthma treatment. Indeed, such therapeutic agents effectively interfere with many pathogenic circuits underpinning asthma. Among these drugs, during the last decades budesonide has been probably the most used molecule in both experimental studies and clinical practice. Therefore, a large body of evidence clearly shows that budesonide, either alone or in combination with long-acting bronchodilators, provides a successful control of asthma in many patients ranging throughout the overall spectrum of disease severity. These excellent therapeutic properties of budesonide basically depend on its molecular mechanisms of action, capable of inhibiting within the airways the activity of multiple immune-inflammatory and structural cells involved in asthma pathobiology.

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Keywords : Budesonide, Glucocorticoids, Asthma


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© 2016  Elsevier Ltd. Tous droits réservés.
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Vol 40

P. 15-21 - octobre 2016 Retour au numéro
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  • Molecularly targeted therapies for asthma: Current development, challenges and potential clinical translation
  • Ibrahim Sulaiman, Jonathan Chee Woei Lim, Hon Liong Soo, Johnson Stanslas

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