Glaser K B, Carlson R P, Sung A, Bauer J, Lock Y W, Holloway D, Sturm R, Hartman D, Walter T, Woeppel S
Wyeth-Ayerst Research, Princeton, NJ 08543.
Agents Actions. 1993;39 Spec No:C30-2. doi: 10.1007/BF01972711.
WAY-121,520 inhibited human synovial fluid PLA2 (HSF-PLA2) (IC50 = 4 microM) using arachidonic acid-labeled E. coli as substrate. Further biochemical characterization of WAY-121,520 demonstrated potent inhibition of 5-lipoxygenase (5-LO) activity in the murine macrophage (LTC4, IC50 = 4 nM) and rat PMN (LTB4, IC50 = 10 nM) and an ability to antagonize LTD4 binding to isolated guinea-pig trachea (pKB = 6.0). In vivo anti-inflammatory activity was noted in murine TPA-induced (ED50 = 91 micrograms/ear) and arachidonic acid-induced (66% inhibition at 400 micrograms/ear) ear edema and in leukotriene-dependent antigen-induced bronchoconstriction in the guinea pig (73% inhibition at 50 mg/kg, p.o.). WAY-121,520 represents a novel series of indomethacin-based inhibitors of PLA2 with anti-inflammatory activity resulting from a combination of biochemical activities (inhibition of 5-LO and PLA2 and LTD4 antagonism). This agent may provide added therapeutic efficacy over more selective inhibitors.
WAY-121,520以花生四烯酸标记的大肠杆菌为底物,抑制人滑液磷脂酶A2(HSF-PLA2)(IC50 = 4微摩尔)。WAY-121,520的进一步生化特性表明,它能有效抑制小鼠巨噬细胞中的5-脂氧合酶(5-LO)活性(白三烯C4,IC50 = 4纳摩尔)和大鼠多形核白细胞中的5-脂氧合酶活性(白三烯B4,IC50 = 10纳摩尔),并具有拮抗白三烯D4与分离的豚鼠气管结合的能力(pKB = 6.0)。在小鼠佛波酯诱导的耳水肿(ED50 = 91微克/耳)和花生四烯酸诱导的耳水肿(400微克/耳时抑制66%)以及豚鼠白三烯依赖性抗原诱导的支气管收缩(口服50毫克/千克时抑制73%)中,观察到WAY-121,520的体内抗炎活性。WAY-121,520代表了一系列基于吲哚美辛的新型磷脂酶A2抑制剂,具有抗炎活性,这是由多种生化活性(抑制5-LO和磷脂酶A2以及拮抗白三烯D4)共同作用产生的。与更具选择性的抑制剂相比,该药物可能具有更高的治疗效果。