Fretland D J, Widomski D L, Zemaitis J M, Djurić S W, Shone R L
Department of Gastrointestinal Research, G.D. Searle and Co., Skokie, Illinois 60077.
Inflammation. 1989 Oct;13(5):601-5. doi: 10.1007/BF00916766.
Leukotriene B4 (LTB4) is a proinflammatory product of arachidonic acid metabolism that has been implicated as a mediator in a number of inflammatory diseases. When injected intradermally into the cavine. LTB4 elicits a dose-dependent immigration (chemotaxis) of neutrophils (PMNs) into the injection sites as assessed by the presence of a neutrophil marker enzyme myeloperoxidase. SC-41930 (7-[3-(4-acetyl-3-methoxy-2-propylphenoxy)propoxy]-3,4-dihydro-8-p ropyl-2H- 1-benzopyran-2-carboxylic acid), a potent LTB4 receptor antagonist inhibited the chemotactic actions of LTB4 when coadministered into the dermal site and when given intravenously or orally with ED50 values of 200 ng, 0.5 mg/kg, and 0.6 mg/kg respectively. This compound may well have application in disease states, such as inflammatory bowel disease and psoriasis, where LTB4 is implicated as a proinflammatory mediator.
白三烯B4(LTB4)是花生四烯酸代谢的促炎产物,在多种炎症性疾病中被认为是一种介质。当皮内注射到豚鼠体内时,通过中性粒细胞标记酶髓过氧化物酶的存在评估,LTB4会引起中性粒细胞(PMN)向注射部位的剂量依赖性迁移(趋化作用)。SC - 41930(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),一种强效的LTB4受体拮抗剂,当与LTB4共同皮内给药时,以及分别以200 ng、0.5 mg/kg和0.6 mg/kg的ED50值静脉内或口服给药时,均能抑制LTB4的趋化作用。该化合物很可能在诸如炎症性肠病和银屑病等疾病状态中有应用,在这些疾病中LTB4被认为是促炎介质。