Nitrosative stress plays an important role in inflammatory diseases of the nasal cavity, therefore the study of its manifestations and the possibilities of its pharmacological correction remains relevant.
OBJECTIVE
To assess the state of nitrosative stress and effectiveness of antioxidant therapy in patients with inflammatory diseases of the nasal cavity.
PATIENTS AND METHODS
A total of 156 patients with inflammation of the nasal cavity, divided into 4 groups according to the factor which caused the inflammation and the treatment methods, were examined. The 1st and 2nd groups included 36 patients with acute rhinosinusitis, the 3rd (44 patients) and 4th (40 patients) groups — patients after septoplasty and vasotomy. Subjects of the 2nd and 4th groups, in addition to standard treatment and topical administration of repairing agent into the nasal cavity, were complementary given an antioxidant — 15% solution of dimethyl ether of 1.1-dimethyl-3-oxybutyl phosphonic acid. Concentration of nitrates and nitrites was determined in the nasal secretion of patients at admission, on the 5th, 10th, 21st day.
RESULTS
In the early observation stages of inflammation, an increase in the concentration of nitrogen oxide metabolites with subsequent depletion of the nitroxidergic system and a gradual decrease of their concentration below the control values have been noted. On the 5th day, statistically significant difference was noted between the 1st and 2nd (p1—2=0.0001), the 3rd and 4th (p3—4=0.009) groups. In the 2nd and 4th groups, the concentration of nitrogen oxide metabolites did not exceed the control values.
CONCLUSIONS
Administration of antioxidant therapy in the early period reduced the appearance of nitrosative stress in patients with inflammatory diseases of the nasal cavity. In order to avoid a pronounced and long-lasting inhibition of nitrogen oxide production after administration of antioxidant therapy, which can have a negative effect on the epithelium regeneration, it is necessary to dynamically control the concentration of nitrogen oxide metabolites in the nasal secretion.