Ko F N, Hsiao G, Chen I S, Wu S J, Teng C M
Pharmacological Institute, College of Medicine, National Taiwan University, Tapei.
Biochem Pharmacol. 1993 Oct 5;46(7):1165-73. doi: 10.1016/0006-2952(93)90465-9.
Avicine pseudocyanide, a derivative of avicine isolated from Zanthoxylum integrifoliolum Merr., inhibited collagen-induced platelet aggregation and release reaction in a concentration-dependent manner. Trimucytin is a collagen-like snake venom protein isolated from Trimeresurus mucrosquamatus. Avicine pseudocyanide also inhibited trimucytin (1 microgram/mL)-induced platelet aggregation and release reaction concentration dependently. The IC50 values of avicine pseudocyanide on collagen (10 micrograms/mL)- and trimucytin (1 microgram/mL)-induced platelet aggregation were 47.3 +/- 4.1 and 62.5 +/- 5.6 microM, respectively. Avicine pseudocyanide at a concentration of 300 microM inhibited less than 30% of platelet aggregation induced by ADP (20 microM), AA (100 microM), U46619 (1 microM), PAF (2 ng/mL) and thrombin (0.1 U/mL). The concentration-response curve of collagen-induced platelet aggregation was shifted to the right by avicine pseudocyanide (20-100 microM) concentration dependently. The Schild plot showed that pA2 and pA10 values of avicine pseudocyanide were 4.8 and 4.3, respectively, with slope of -1.9. Avicine pseudocyanide also inhibited collagen (10 micrograms/mL)-induced aggregation of rabbit whole blood with an IC50 of 145 +/- 13 microM. Collagen-induced thromboxane B2 formation was also inhibited by avicine pseudocyanide in a concentration-dependent manner with a maximal effect at 100 microM. However, arachidonic acid (AA)-induced thromboxane B2 and prostaglandin D2 formations were only partially suppressed by a high concentration of avicine pseudocyanide (300 microM). Avicine pseudocyanide (100 microM) inhibited the [3H]inositol monophosphate formation and the rise of intracellular Ca2+ concentration caused by collagen but not those caused by AA, U46619, platelet-activating factor and thrombin. In the presence of prostaglandin E1, Mg(2+)-dependent platelet adhesion to collagen was inhibited by avicine pseudocyanide with an IC50 of 278 +/- 16 microM. These data indicate that avicine pseudocyanide is an inhibitor of collagen-induced platelet aggregation and platelet-collagen adhesion.
从全缘叶花椒中分离得到的阿维辛假氰化物是阿维辛的衍生物,它能以浓度依赖的方式抑制胶原诱导的血小板聚集和释放反应。竹叶青毒素是从竹叶青蛇中分离得到的一种类胶原蛇毒蛋白。阿维辛假氰化物也能浓度依赖性地抑制竹叶青毒素(1微克/毫升)诱导的血小板聚集和释放反应。阿维辛假氰化物对胶原(10微克/毫升)和竹叶青毒素(1微克/毫升)诱导的血小板聚集的IC50值分别为47.3±4.1和62.5±5.6微摩尔。300微摩尔浓度的阿维辛假氰化物对ADP(20微摩尔)、花生四烯酸(AA,100微摩尔)、U46619(1微摩尔)、血小板活化因子(PAF,2纳克/毫升)和凝血酶(0.1单位/毫升)诱导的血小板聚集的抑制率小于30%。阿维辛假氰化物(20 - 100微摩尔)能使胶原诱导的血小板聚集浓度反应曲线依浓度向右移动。Schild图显示阿维辛假氰化物的pA2和pA10值分别为4.8和4.3,斜率为 - 1.9。阿维辛假氰化物也能抑制胶原(10微克/毫升)诱导的兔全血聚集,IC50为145±13微摩尔。阿维辛假氰化物还能以浓度依赖的方式抑制胶原诱导的血栓素B2形成,在100微摩尔时效果最佳。然而,高浓度(300微摩尔)的阿维辛假氰化物只能部分抑制花生四烯酸(AA)诱导的血栓素B2和前列腺素D2形成。阿维辛假氰化物(100微摩尔)能抑制胶原引起的[3H]肌醇单磷酸形成和细胞内Ca2 +浓度升高,但不能抑制AA、U46619、血小板活化因子和凝血酶引起的上述变化。在前列腺素E1存在的情况下,阿维辛假氰化物能抑制Mg(2 +)依赖的血小板与胶原的黏附,IC50为278±16微摩尔。这些数据表明阿维辛假氰化物是胶原诱导的血小板聚集和血小板 - 胶原黏附的抑制剂。