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1"G. P. Livanos and M. Simou" Laboratories, Evangelismos Hospital, Department of Critical Care and Pulmonary Services, University of Athens School of Medicine, Athens; 2Laboratory of Molecular Pharmacology, Department of Pharmacy, University of Patras, Patras; and 3Center for Immunology and Transplantation, Institute for Biomedical Research, Academy of Athens, Athens, Greece
Submitted 26 July 2005 ; accepted in final form 27 August 2005
Soluble guanylyl cyclase (sGC) is an enzyme highly expressed in the lung that generates cGMP contributing to airway smooth muscle relaxation. To determine whether the bronchoconstriction observed in asthma is accompanied by changes in sGC expression, we used a well-established murine model of allergic asthma. Histological and biochemical analyses confirmed the presence of inflammation in the lungs of mice sensitized and challenged with ovalbumin (OVA). Moreover, mice sensitized and challenged with OVA exhibited airway hyperreactivity to methacholine inhalation. Steady-state mRNA levels for all sGC subunits (
1,
2, and
1) were reduced in the lungs of mice with allergic asthma by 6080%, as estimated by real-time PCR. These changes in mRNA were paralleled by changes at the protein level:
1,
2, and
1 expression was reduced by 5080% as determined by Western blotting. Reduced
1 and
1 expression in bronchial smooth muscle cells was demonstrated by immunohistochemistry. To study if sGC inhibition mimics the airway hyperreactivity seen in asthma, we treated naïve mice with a selective sGC inhibitor. Indeed, in mice receiving ODQ the methacholine dose response was shifted to the left. We conclude that sGC expression is reduced in experimental asthma contributing to the observed airway hyperreactivity.
nitric oxide; guanosine 3',5'-cyclic monophosphate, airway hyperreactivity; bronchoconstriction
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