N-Acetyl-aspartyl-glutamic acid inhibits cellular recruitment and mediator release during the late allergen-induced nasal reaction

European Journal of Clinical Pharmacology - Tập 54 - Trang 515-520 - 1998
A. Miadonna1, N. Milazzo1, C. Salmaso1, M. Cottini2, M. Lorini1, A. Tedeschi1
1Respiratory Allergy and Immunology Unit, Third Division of Internal Medicine, IRCCS Ospedale Maggiore Policlinico, Via F. Sforza 35, I-20122 Milan, Italy Tel.: +39-2-55033383; Fax: +39-2-55192842, , IT
2Allergy and Pneumology Unit, ASL 12, Bergamo Italy, , IT

Tóm tắt

Objective: N-acetyl-aspartyl-glutamic acid (NAAGA) was effective in the treatment of allergic rhinitis, with an action on early allergen-induced nasal symptoms and mediator release. The aim of this study was to evaluate the clinical activity of NAAGA and its effects on the late antigen-induced reaction in the nose. Methods: Ten patients with allergic seasonal rhinitis were included in this randomized double-blind crossover trial of a 6% wt/vol solution of NAAGA (daily dosage 84 mg) versus placebo (lactose). The drug and placebo were administered intranasally five times daily for 1 week, with a 2-week interval between treatments. Results: Treatment with NAAGA, but not with placebo, significantly reduced the late antigen-induced nasal symptoms, mainly nasal obstruction. Eosinophil numbers in the nasal lavages collected 6 h and 24 h after challenge were significantly lower after NAAGA than after placebo. Active treatment also significantly reduced the neutrophil count 6 h after antigen challenge, and significantly lowered eosinophil cationic protein and myeloperoxidase levels in nasal lavages 6 h and 24 h after antigen challenge. Conclusion: These results indicate that treatment for 1 week with NAAGA can reduce the late antigen-induced reaction in the nose. This is accompanied by a reduction in eosinophil and neutrophil recruitment and release of eosinophil cationic protein and myeloperoxidase.