Nimesulide in cystic fibrosis treatment
Abstract
The purpose of our study was to examine the antiinflammatory effect of nimesulide the novel selective cyclooxygenase-2 inhibitor. Fifteen CF patients (the mean age 11.9 years) were treated with basic therapy and nimesulide in the daily dose of 3 mg per kg of the body weight. Inflammatory markers in the sputum samples (neutrophil elastase activity, TNF-α and IL-8 concentrations) and in peripheral blood (sensitivity of lymphocytes to antiproliferative effect of glucocorticoids and plasma TNF-α level) have been determined. During the six-month period before the start of Nimesulide, most patients had experienced a decline in FEV1 and FVC. Following the nimesulide treatment the lung disease progression became slower. The patients with poor lung function showed an essential elevation of neutrophil elastase activity and decrease of TNF-α in their sputa. Authors postulate that elastase activity elevation is associated with the destruction of neutrophils following the antiinflammatory treatment. Decrease in plasma concentrations of TNF-α as well as in the number of activated lymphocytes in peripheral blood is an evidence of the systemic antiinflammatory effect of nimesulide.
About the Authors
A. L. PukhalskyRussian Federation
L. A. Shabalova
Russian Federation
G. V. Shmarina
Russian Federation
N. I. Kapranov
Russian Federation
S. I. Kokarovtseva
Russian Federation
References
1. Певницкий Л.А., Пухальский А.Л., Капранов И.И. и др. Иммунологический мониторинг больных муковисцидозом. Значение различных лабораторных показателей. Вестн. РАМН 2000; 5: 40—46.
2. Bolten W.W. Scientific rationale for specific inhibition of COX-2. J. Rheumatol. 1998; suppl.51: 2—7.
3. Botting J. Cox-2: Selective inhibitors in clinical trials. Drug News Perspect. 1996; 9: 123—128.
4. Dallegri F., Ottonello L ., Dapino P., Sacchetti C. Effect of nonsteroidal antiinflammatory drugs on the neutrophil promoted inactivation of a -1-proteinase inhibitor. J. Rheumatol. 1992; 19: 419—423.
5. Famaey J.P. In vitro and in vivo pharmacological evidence of selective cyclooxygenase-2 inhibition by nimesulide: an overview. Inflam. Res. 1997; 46: 437—446.
6. Pukhalsky A.L., Kalashnikova E.A., Lyashko V.N., Pevnitsky L.A. Inhibition of phytohemagglutinin-induced lymphocyte proliferation by dexamethasone: mechanisms of individual susceptibility. Int. J. Immunopharmacol. 1990; 12: 657—663.
7. Pukhalsky A.L., Kapranov N.I., Kalashnikova E.A. et al. Inflammatory markers in cystic fibrosis patients with lung Pseudomonas aerugonosa infection. Mediators Inflam. 1999; 8: 159—167.
8. Rabasseda X. Nimesulide: A selective cyclooxygenase 2 inhibitor antiinflammatory drug. Drugs Today 1996; 32 (suppl.D): IS—23S.
9. Stuhlmeier K.M., Li H., Kao J.J. Ibuprofen: New explanation for an old phenomenon. Biochem. Pharmacol. 1999; 57: 313—320.
10. Wanner G.A., Muller P., Ertel W. et al. Differential effect of cyclooxygenase metabolites on proinflammatory cytokine release by Kupffer cells after liver ischemia and repefusion. Am. J. Surg. 1998; 175: 146—151.
Review
For citations:
Pukhalsky A.L., Shabalova L.A., Shmarina G.V., Kapranov N.I., Kokarovtseva S.I. Nimesulide in cystic fibrosis treatment. PULMONOLOGIYA. 2001;(3):46-50. (In Russ.)