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Roflumilast N-Oxide in Combination with Formoterol Enhances the Antiinflammatory Effect of Dexamethasone in Airway Smooth Muscle Cells.
Patel, Brijeshkumar S; Rahman, Md Mostafizur; Baehring, Gina; Xenaki, Dikaia; Tang, Francesca Su-May; Oliver, Brian G; Ammit, Alaina J.
Afiliação
  • Patel BS; 1 Faculty of Pharmacy and.
  • Rahman MM; 1 Faculty of Pharmacy and.
  • Baehring G; 2 Woolcock Emphysema Centre and.
  • Xenaki D; 3 Respiratory Cellular and Molecular Biology, Woolcock Institute of Medical Research, University of Sydney, Sydney, New South Wales, Australia; and.
  • Tang FS; 2 Woolcock Emphysema Centre and.
  • Oliver BG; 2 Woolcock Emphysema Centre and.
  • Ammit AJ; 3 Respiratory Cellular and Molecular Biology, Woolcock Institute of Medical Research, University of Sydney, Sydney, New South Wales, Australia; and.
Am J Respir Cell Mol Biol ; 56(4): 532-538, 2017 04.
Article em En | MEDLINE | ID: mdl-27997807
ABSTRACT
Roflumilast is an orally active phosphodiesterase 4 inhibitor approved for use in chronic obstructive pulmonary disease. Roflumilast N-oxide (RNO) is the active metabolite of roflumilast and has a demonstrated antiinflammatory impact in vivo and in vitro. To date, the effect of RNO on the synthetic function of airway smooth muscle (ASM) cells is unknown. We address this herein and investigate the effect of RNO on ß2-adrenoceptor-mediated, cAMP-dependent responses in ASM cells in vitro, and whether RNO enhances steroid-induced repression of inflammation. RNO (0.001-1,000 nM) alone had no effect on AMP production from ASM cells, and significant potentiation of the long-acting ß2-agonist formoterol-induced cAMP could only be achieved at the highest concentration of RNO tested (1,000 nM). At this concentration, RNO exerted a small, but not significantly different, potentiation of formoterol-induced expression of antiinflammatory mitogen-activated protein kinase phosphatase 1. Consequently, tumor necrosis factor-induced IL-8 secretion was unaffected by RNO in combination with formoterol. However, because there was the potential for phosphodiesterase 4 inhibitors and long-acting ß2-agonists to interact with corticosteroids to achieve superior antiinflammatory efficacy, we examined whether RNO, alone or in combination with formoterol, enhanced the antiinflammatory effect of dexamethasone by measuring the impact on IL-8 secretion. Although RNO alone did not significantly enhance the cytokine repression achieved with steroids, RNO in combination with formoterol significantly enhanced the antiinflammatory effect of dexamethasone in ASM cells. This was linked to increased mitogen-activated protein kinase phosphatase 1 expression in ASM cells, suggesting that a molecular mechanism is responsible for augmented antiinflammatory actions of combination therapeutic approaches that include RNO.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzamidas / Dexametasona / Miócitos de Músculo Liso / Fumarato de Formoterol / Aminopiridinas / Pulmão / Anti-Inflamatórios Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzamidas / Dexametasona / Miócitos de Músculo Liso / Fumarato de Formoterol / Aminopiridinas / Pulmão / Anti-Inflamatórios Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article