Villani-Price D, Yang D C, Walsh R E, Fretland D J, Keith R H, Kocan G, Kachur J F, Gaginella T S, Tsai B S
Gastrointestinal Diseases Research, Searle Research and Development, Skokie, Illinois.
J Pharmacol Exp Ther. 1992 Jan;260(1):187-91.
7-[3-(4-acetyl-3-methoxy-2-propylphenoxy)-propoxy]-3,4-dihydro-8- propyl-2H-1-benzopyran-2-carboxylic acid (SC-41930), a leukotriene B4 (LTB4) receptor antagonist with anti-inflammatory activity in animal models of colitis, was evaluated for effects on superoxide, LTB4 and prostaglandin E2 production. SC-41930 inhibited human neutrophil (PMN) superoxide generation maximally stimulated by f-Met-Leu-Phe (IC50 4 microM) and C5a (IC50 approximately 12 microM). Moreover, postreceptor stimulation of superoxide production by NaF (a G protein activator), but not by phorbol myristate acetate, was significantly inhibited by SC-41930, indicating that SC-41930 may act via attenuation of a G protein-mediated signal transduction. SC-41930 also inhibited A23187-stimulated LTB4 production (IC50 5.3 microM) in human PMN as well as LTB4 (IC50 2.1 microM) and prostaglandin E2 (IC50 2.9 microM) production in HL-60 cells. When coinjected intradermally (400 micrograms/site), SC-41930 inhibited A23187-stimulated increases in LTB4 levels in guinea pig skin. SC-41930 inhibited human synovial phospholipase A2 (IC50 72 microM), A23187-stimulated 5-hydroxy-eicosatetranoic acid production in human PMN (IC50 8.5 microM), and rat peritoneal leukotriene A4 hydrolase (IC50 20 microM), but not ram seminal vesical cyclooxygenase. The results suggest that the anti-inflammatory activity of SC-41930 could be attributed to postreceptor inhibition of inflammatory mediator production by PMN and other cells in addition to antagonism of PMN LTB4 receptors.
7-[3-(4-乙酰基-3-甲氧基-2-丙基苯氧基)-丙氧基]-3,4-二氢-8-丙基-2H-1-苯并吡喃-2-羧酸(SC-41930)是一种在结肠炎动物模型中具有抗炎活性的白三烯B4(LTB4)受体拮抗剂,已对其对超氧化物、LTB4和前列腺素E2生成的影响进行了评估。SC-41930最大程度地抑制了由f-甲硫氨酰-亮氨酰-苯丙氨酸(IC50为4 microM)和C5a(IC50约为12 microM)刺激的人中性粒细胞(PMN)超氧化物生成。此外,SC-41930显著抑制了由NaF(一种G蛋白激活剂)而非佛波酯肉豆蔻酸酯对超氧化物生成的受体后刺激,这表明SC-41930可能通过减弱G蛋白介导的信号转导起作用。SC-41930还抑制了人PMN中由A23187刺激的LTB4生成(IC50为5.3 microM)以及HL-60细胞中LTB4(IC50为2.1 microM)和前列腺素E2(IC50为2.9 microM)的生成。当皮内注射(400微克/部位)时,SC-41930抑制了豚鼠皮肤中由A23187刺激的LTB4水平升高。SC-41930抑制了人滑膜磷脂酶A2(IC50为72 microM)、人PMN中由A23187刺激的5-羟基二十碳四烯酸生成(IC50为8.5 microM)以及大鼠腹膜白三烯A4水解酶(IC50为20 microM),但不抑制公羊精囊环氧化酶。结果表明,SC-41930的抗炎活性除了拮抗PMN的LTB4受体外,还可归因于对PMN和其他细胞炎性介质生成的受体后抑制。