Haneberg B, Sørnes S, Bakke O, Solberg C O
Medical Department B, University of Bergen, Norway.
Acta Pathol Microbiol Immunol Scand C. 1987 Aug;95(4):149-53. doi: 10.1111/j.1699-0463.1987.tb00023.x.
A selective zymosan-induced release of lysozyme from freshly prepared human blood granulocytes and monocytes was inhibited by indomethacin, sulindac, piroxicam and ibuprofen. This effect was slightly more marked for granulocytes than for monocytes. Salicylic acid, acetylsalicylic acid and naproxen, even at high concentrations, did not inhibit the enzyme release from either cell type. Since all these nonsteroidal anti-inflammatory agents are cyclooxygenase inhibitors, these findings suggest that lysozyme release is independent of prostaglandin biosynthesis.
新鲜制备的人血粒细胞和单核细胞经酵母聚糖诱导的溶菌酶选择性释放受到吲哚美辛、舒林酸、吡罗昔康和布洛芬的抑制。这种作用在粒细胞中比在单核细胞中略为明显。水杨酸、乙酰水杨酸和萘普生即使在高浓度下也不抑制这两种细胞类型的酶释放。由于所有这些非甾体抗炎药都是环氧化酶抑制剂,这些发现表明溶菌酶的释放与前列腺素生物合成无关。