Selectivity of cyclo-oxygenase inhibitors in human pulmonary epithelial and smooth muscle cells

Cyclo-oxygenase (COX) inhibitors may have a role in reducing inflammation i n asthma and other pulmonary diseases. COX inhibitors have different select ivities for the two COX isoenzymes (COX 1 and COX 2) which vary between pur ified enzyme and intact cell preparations. The relative selectivity of COX inhibitors has not been studied in human airway cells, A number of COX inhibitors in cultured human airway cells were compared whi ch exclusively express either COX 1 (primary degree cultured human airway s mooth muscle (HASM) cells) or COX 2 (A549 pulmonary epithelial cell-line) a s measured by Western blotting. COX activity was assayed by prostaglandin CPG)E-2 production following 30 m in incubation with 5 mM arachidonic acid. COX activity in both cell types w as similar; HASM cells 92.2+/-12.1 ng PGE(2).mg(-1) protein, A549 cells 87. 7+/-24.4 ng PGE(2).mg(-1) protein. In HASM cells the median inhibitory conc entration (IC50) was >10(-5) M for nimesulide, 3.2 x 10(-6) M for N-(2-cycl ohexyloxy-nitrophenyl)-methanesulphonamide (NS398), 1.8 x 10(-8) M for flur biprofen, 6.7 x 10(-9) M for indomethacin and >10(-5) M for aspirin. In A54 9 cells the IC50 was 1.8 x 10(-9) M for nimesulide, 4.1 x 10(-9) M for NS39 8, 6.2 x 10(-10) M for flurbiprofen, 1.3 x 10(-8) M for indomethacin and >1 0(-5) M for aspirin. Sodium valerate had no effect in either HASM or A549 c ells. The COX 2:COX 1 selectivity ratio (COX 2 IC50/COX 1 IC50) was <0.0001 for nimesulide, 0.001 for NS398, 0.03 for flurbiprofen and 1.9 for indomet hacin, In conclusion the present study has shown that cyclo-oxygenase inhibitors h ave a range of selectivities for cyclo-oxygenase 1 and cyclo-oxygenase 2 in intact human airway cells. The relative cyclo-oxygenase 2 selectivity of N -(2-cyclohexyloxy-4-nitrophenyl)-methanesulphonamide and nimesulide may hav e implications for the treatment of asthma and other inflammatory pulmonary diseases.