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Open Access

Reduction of soluble guanylyl cyclase expression in asthma

  • Andreas Papapetropoulos1, 2Email author,
  • Davina de CM Simoes2,
  • Georgia Xanthou3,
  • Charis Roussos1 and
  • Christina Gratziou1
BMC Pharmacology20055(Suppl 1):P42

https://doi.org/10.1186/1471-2210-5-S1-P42

Published: 16 June 2005

Soluble guanylyl cyclase (sGC) is a ubiquitously expressed enzyme that is highly expressed in the lung. Stimulation of sGC by nitric oxide (NO) increases the conversion of GTP to cGMP, thereby, causing airway smooth muscle relaxation. To determine whether sGC expression is reduced in an animal model of inflammatory airway disease and, therefore, contributes to airway hyperreactivity (AHR), mice were sensitized and challenged with ovalbumin (OVA). Histological and biochemical analyses confirmed the presence of inflammation in the lungs of OVA-challenged mice that was characterized by increased eosinophil infiltration, mucus production and high interleukin-13 levels. Moreover, OVA-challenged mice exhibited increased airway reactivity to methacholine inhalation. Steady-state mRNA levels for all sGC subunits (α1, α2 and β1) were reduced in the lungs of OVA mice by 60–80%, as estimated by real-time PCR. The changes in sGC expression extended to the protein level where α1, α2 and β1 were reduced by 50–70%, as determined by western blotting. Reduced α1 and β1 expression in animals with asthma was confirmed by immunohistochemistry and showed to occur in epithelial and smooth muscle cells. To study if AHR and/or inflammation occur following sGC inhibition in naïve animals, mice we treated with the selective sGC inhibitor 1H-[1,2,4] oxydiazolo[4,3-ea]quinoxalin-1-one (ODQ). Such treatment led to bronchial hyperreactivity to methacholine. However, in the bronchoalveolar lavage fluid of ODQ-treated mice only a small increase in macrophage number was detected, without changes in IL-13 levels or eosinophil infiltration. We conclude that sGC expression is reduced in an animal model of asthma contributing to the observed AHR.

Authors’ Affiliations

(1)
G.P. Livanos and M. Simou Laboratories, Evangelismos Hospital, Department of Critical Care and Pulmonary Services, University of Athens School of Medicine
(2)
Laboratory of Molecular Pharmacology, Department of Pharmacy, University of Patras
(3)
Center for Immunology and Transplantation, Institute for Biomedical Research, Academy of Athens

Copyright

© BioMed Central Ltd 2005

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