Kotyuk B, Raychaudhuri A, DiPasquale G
Research Department, Ciba-Geigy Corporation, Summit, NJ 07901.
Agents Actions. 1993;39 Spec No:C46-8. doi: 10.1007/BF01972716.
The arachidonic acid (AA)-induced ear edema model in the mouse has been demonstrated as an effective in vivo experimental tool to screen compounds showing anti-inflammatory activity. Since neutrophil influx is a component of the inflammatory reaction, we have modified this assay by quantitating myeloperoxidase (MPO) levels which reflect neutrophil accumulation in the edematous biopsies of the mouse ear. Our work has shown that orally administered 5-lipoxygenase inhibitors, dual inhibitors (CO/LO), and steroids dose-dependently inhibit both edema formation and MPO activity, whereas oral activity is not seen with NSAID's. There is a good correlation between the inhibition of edema formation and of MPO activity by these compounds. Thus, measurement of MPO, in addition to the AA-induced edema in the mouse ear, can provide another parameter to profile potential anti-inflammatory compounds.
花生四烯酸(AA)诱导的小鼠耳部水肿模型已被证明是筛选具有抗炎活性化合物的一种有效的体内实验工具。由于中性粒细胞浸润是炎症反应的一个组成部分,我们通过定量髓过氧化物酶(MPO)水平对该试验进行了改进,MPO水平反映了小鼠耳部水肿活检组织中中性粒细胞的聚集情况。我们的研究表明,口服5-脂氧合酶抑制剂、双重抑制剂(CO/LO)和类固醇能剂量依赖性地抑制水肿形成和MPO活性,而NSAID则未见口服活性。这些化合物对水肿形成和MPO活性的抑制之间存在良好的相关性。因此,除了测量AA诱导的小鼠耳部水肿外,MPO的测量还可以为潜在抗炎化合物的分析提供另一个参数。