Effect of Cyclooxygenase-2 Specific Inhibitor (SC-58635) on the Production of Nitric Oxide and Prostaglandin E2 in Lipopolysaccharide-stimulated Macrophage Cells.
- Author:
Seung Jae HONG
1
;
Hyung In YANG
;
Hwi Joong YOON
;
Myoung Soo LEE
;
Hyo Jong KANG
;
Wan Uk KIM
;
Sang Heon LEE
;
Chul Soo CHO
;
Ho Youn KIM
Author Information
- Publication Type:Original Article
- Keywords: Celecoxib; nitric oxide; COX-2; NF-kappaB; PGE2
- MeSH: Arthritis, Rheumatoid; Blotting, Western; Celecoxib; Cyclooxygenase 2*; Dinoprostone*; Hydrocortisone; Inflammation; Inflammation Mediators; Macrophages*; NF-kappa B; Nitric Oxide*
- From:Immune Network 2003;3(1):69-77
- CountryRepublic of Korea
- Language:Korean
- Abstract: BACKGROUND: Celecoxib, a COX-2 specific inhibitor, has recently been used for the treatment of rheumatoid arthritis. However, the molecular and cellular mechanisms of celecoxib against RA inflammation remain to be defined. To elucidate the action mechanism of celecoxib on inflammatory cells, we investigated the effect of celecoxib on the production of two important mediators of inflammation, nitric oxide and PGE2 METHODS: RAW 264.7 cells stimulated with LPS were preincubated with various concentrations of celecoxib (from 10(-8) to 10(-5) M) and 10muM hydrocortisone, respectively. The production of NO and PGE2, the end products of iNOS and COX-2 genes, were estimated in culture supernatants by Greiss method and EIA, respectively. The expression of iNOS gene, COX-2 gene, NF-kappaB, and I-kappaB were determined by RT-PCR and western blot analysis. RESULTS: Celecoxib and hydrocortisone inhibited the production of NO and PGE2 in dose dependent manner, when RAW 264.7 cells were stimulated with LPS. The expression of iNOS was also down-regulated by celecoxib and hydrocortisone. Interestingly, COX-2 gene differentially expressed according to the dose of celecoxib, a decrease with lower dose (10(-8) M) but an increase with higher dose (10(-5) M). NF-kappaB binding activity was decreased by lower dose of celecoxib, whereas was not affected by higher dose of it. The expression of I-kappaB was suppressed by higher dose of celecoxib. CONCLUSION: The celecoxib strongly suppressed the production of NO and PGE2 in LPS-stimulated RAW264.7 cells. The decrease of NO seems to be linked to the inhibition of iNOS by celecoxib. The lower and higher dose of celecoxib differentially regulated the COX-2 expression and NF-kappaB activity
