epiyangambin的药理学特征:具有PAF拮抗剂活性的呋喃木脂素。

Journal of lipid mediators Pub Date : 1993-05-01
H C Castro-Faria-Neto, M A Martins, P M Silva, P T Bozza, H N Cruz, M de Queiroz-Paulo, M A Kaplan, R S Cordeiro
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引用次数: 0

摘要

研究了呋喃木脂素epiyangambin对paf诱导的兔体外血小板聚集和大鼠血小板减少的抑制作用。Epiyangambin剂量依赖性地抑制paf诱导的血小板聚集,而不改变最大反应的幅度,表明竞争性拮抗剂。epiyangambin对10(-9)M paf诱导聚集的IC50值为6.1 × 10(-7) M, Schild分析得出pA2为6.91 +/- 0.2,斜率为0.98 +/- 0.25 (n = 4), pKb为6.94 +/- 0.19。Epiyangambin对胶原、凝血酶、ADP诱导的血小板聚集无影响。体内给药20 mg/kg木脂素可显著抑制paf诱导的大鼠血小板减少症。这些数据表明,epiyangambin在体外和体内都是一种有效的选择性PAF拮抗剂。
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Pharmacological profile of epiyangambin: a furofuran lignan with PAF antagonist activity.

The ability of a furofuran lignan, epiyangambin, to inhibit PAF-induced rabbit platelet aggregation in vitro and thrombocytopenia in rats was investigated. Epiyangambin dose-dependently inhibited PAF-induced platelet aggregation without modifying the amplitude of the maximal response, indicating a competitive antagonism. The IC50 value of epiyangambin for 10(-9) M PAF-induced aggregation was 6.1 x 10(-7) M and the Schild analysis provided a pA2 of 6.91 +/- 0.2 with a slope of 0.98 +/- 0.25 (n = 4) and a pKb of 6.94 +/- 0.19. Epiyangambin had no effect upon the platelet aggregation induced by collagen, thrombin or ADP. The in vivo administration of the lignan at 20 mg/kg significantly inhibited PAF-induced thrombocytopenia in rats. These data indicate that epiyangambin is a potent and selective antagonist of PAF both in vitro and in vivo.

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