Killackey J J, Killackey B A, Cerskus I, Philp R B
Inflammation. 1984 Jun;8(2):157-69. doi: 10.1007/BF00916091.
3-Hydroperoxy-3-methylphthalide (3-HMP), a structural analog of acetylsalicylic acid (ASA), was found to have some antiinflammatory properties which are distinct from those of ASA. 3-HMP inhibits human platelet aggregation and ATP release in response to low concentrations of collagen but is less effective than ASA. 3-HMP inhibits prostaglandin and thromboxane production from exogenous [14C]arachidonic acid by human platelet lysates in vitro and does so at lower concentrations than ASA (3-HMP IC50 = 10 microM; ASA IC50 = 50 microM). 3-HMP is also more effective than ASA as an inhibitor of prostacyclin-like activity production by rings of rabbit aorta. Human polymorphonuclear (PMN) leukocyte [14C]arachidonic acid metabolism is inhibited by 3-HMP but not ASA. In urethane-anesthetized rats, 3-HMP (10 mg/kg intravenously) is effective in inhibiting PMN leukocyte accumulation in response to intrapleural carrageenan administration whereas ASA is ineffective (100 mg/kg intravenously). This hydroperoxy analog of ASA has antiinflammatory activity which may result from a combination of the ASA-like and hydroperoxide-related pharmacological properties.
3-氢过氧基-3-甲基苯酞(3-HMP)是乙酰水杨酸(ASA)的结构类似物,已发现其具有一些与ASA不同的抗炎特性。3-HMP可抑制低浓度胶原蛋白诱导的人血小板聚集和ATP释放,但效果不如ASA。3-HMP在体外可抑制人血小板裂解物从外源性[14C]花生四烯酸生成前列腺素和血栓素,且所需浓度低于ASA(3-HMP的IC50 = 10 microM;ASA的IC50 = 50 microM)。作为兔主动脉环生成前列环素样活性的抑制剂,3-HMP也比ASA更有效。3-HMP可抑制人多形核(PMN)白细胞的[14C]花生四烯酸代谢,而ASA则无此作用。在氨基甲酸乙酯麻醉的大鼠中,3-HMP(静脉注射10 mg/kg)可有效抑制胸膜内注射角叉菜胶后PMN白细胞的聚集,而ASA(静脉注射100 mg/kg)则无效。这种ASA的氢过氧基类似物具有抗炎活性,可能是ASA样和氢过氧化物相关药理特性共同作用的结果。