Original Articles: Rhinitis, Sinusitis, Upper Airway DiseasesNasal mucosal expression of nitric oxide synthases in patients with allergic rhinitis and its relation to asthma
Section snippets
INTRODUCTION
Nitric oxide (NO) is a short-lived, lipophilic free radical that is synthesized from arginine by the action of NO synthase (NOS), which has 3 forms, including constitutive neuronal NOS (nNOS), inducible NOS (iNOS), and constitutive endothelial or epithelial NOS (eNOS). 1, 2, 3, 4 NO is found in higher concentrations in upper airways when compared with the lower airways in healthy individuals. 5 NO has contradictory roles in the pathophysiology of allergic inflammation in both allergic rhinitis
Participants and Study Design
Seventeen patients (10 women and 7 men) with seasonal AR were enrolled in this study along with 9 patients (5 women and 4 men) with nasal septum deviation as the nonallergic control group. Ethical concerns prohibited enrollment of a healthy control group in the study. In patients with seasonal AR, the mean ± SD age was 26.52 ± 5.91 years (age range, 19-37 years). Diagnosis of seasonal AR was based on history, physical examination, and skin testing. Allergic sensitization was demonstrated by
RESULTS
The expression of eNOS in patients with seasonal AR and nonallergic controls was similar. The HSCORE for eNOS in seasonal AR was 1.85 ± 0.78, whereas that in the nonallergic control was 1.63 ± 0.54 (P = .12) Figure 1, Figure 2. On the other hand, a significant difference was found between expressions of iNOS in the 2 groups. The HSCORE for iNOS in the seasonal AR group was 1.75 ± 0.75 and that in the nonallergic control group was 0.71 ± 0.6 (P = .004) Figure 3, Figure 4.
When patients with
DISCUSSION
NO is a short-lived, lipophilic free radical that activates guanylyl cyclase, which catalyzes the formation of guanosine monophosphate that has a role in smooth muscle relaxation, immune regulation, many physiologic organizations, and cell to cell communication. 15, 16 It has dual effects on airway: weak bronchodilation that might be beneficial and cytotoxicity and inflammation that are deleterious. 17 Furthermore, it suppresses T-cell proliferation and TH1 cell response, favoring TH2 response
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Disclosures: Authors have nothing to disclose.