Literature DB >> 26623399

Rolipram: Eotaxin and phosphodiesterase IV inhibitor versus bronchial hyper-reactivity response.

Hamza Hassan Khan1, Salman Assad1, Muhammad Aadil Rahman1, Asfandyar Khan Niazi1.   

Abstract

Entities:  

Year:  2015        PMID: 26623399      PMCID: PMC4638055          DOI: 10.4103/2277-9175.166647

Source DB:  PubMed          Journal:  Adv Biomed Res        ISSN: 2277-9175


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Sir, I am writing this letter to comment on several previously published articles on the use of phosphodiesterase (PDE) 3 in combination with PDE 4 in patients with bronchial hyper-reactivity.[12] These articles suggest the superiority of this combination over conventional treatment; however, as discussed later, rolipram, an investigational PDE 4 inhibitor, may comparatively prove to be more beneficial when used in combination with a beta-agonist and corticosteroids. Bronchial hyper-reactivity responses involve bronchial inflammation characterized by activation and accumulation of dendritic cells, eosinophils, mast cells, macrophages, T-lymphocytes, and tissue remodeling process.[3] Eotaxin, a chemo-attractant, causes up regulation of CD11b, eosinophil accumulation during an allergic response in lungs, and shedding of L-selectin in human eosinophils. Rolipram inhibits CD11b up regulations as well as eotaxin-induced trans-endothelial movement of eosinophils causing inhibition of eosinophil recruitment. In addition, rolipram also inhibit tumor necrosis factor (TNF)-alpha, at both mRNA and protein levels, thus enhancing its anti-inflammatory effects.[4] Moreover, Since PDE 4 enzymes are widely present in the respiratory tract that makes them susceptible to their inhibition by local application therefore inhaled administration of PDE 4 inhibitor has shown considerably more improvement.[5] On the other hand, beta-agonist cause bronchodilation therefore the synergistic effect of beta-agonist with PDE 4 inhibitor is indicated by inhibition of antigen-induced contraction and reduction of increase in vascular permeability which are key factors responsible for the patho-physiology of allergic diseases like asthma.[4] Furthermore, corticosteroids such as dexamethasone and fluticasone also partially reduce the release of eotaxin. The combined use of β2-agonists, rolipram, and steroids abolished TNF-α-induced eotaxin release and hence their combination has additive beneficial effects in the treatment of the eosinophilia associated with asthma and other allergic diseases. Rolipram, being an investigational drug, should be combined with salbutamol and corticosteroids for the management of asthma. In addition, specific eotaxin inhibitors need to be identified that may not only help us to rectify asthmatic problems, but also leads to avoidance of asthmatic exacerbations and most other infections leading to eosinophilia.
  4 in total

1.  Superiority of combined phosphodiesterase PDE3/PDE4 inhibition over PDE4 inhibition alone on glucocorticoid- and long-acting β2-adrenoceptor agonist-induced gene expression in human airway epithelial cells.

Authors:  Hawazen BinMahfouz; Bibhusana Borthakur; Dong Yan; Tresa George; Mark A Giembycz; Robert Newton
Journal:  Mol Pharmacol       Date:  2014-10-16       Impact factor: 4.436

2.  Oxidative stress-induced glucocorticoid resistance is prevented by dual PDE3/PDE4 inhibition in human alveolar macrophages.

Authors:  J Milara; A Navarro; P Almudéver; J Lluch; E J Morcillo; J Cortijo
Journal:  Clin Exp Allergy       Date:  2011-04       Impact factor: 5.018

Review 3.  Dual PDE3/4 and PDE4 inhibitors: novel treatments for COPD and other inflammatory airway diseases.

Authors:  Katharine H Abbott-Banner; Clive P Page
Journal:  Basic Clin Pharmacol Toxicol       Date:  2014-03-06       Impact factor: 4.080

4.  Poly(ADP-ribose) polymerase inhibition with HYDAMTIQ reduces allergen-induced asthma-like reaction, bronchial hyper-reactivity and airway remodelling.

Authors:  Laura Lucarini; Alessandro Pini; Elisabetta Gerace; Roberto Pellicciari; Emanuela Masini; Flavio Moroni
Journal:  J Cell Mol Med       Date:  2014-01-20       Impact factor: 5.310

  4 in total

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