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瑞香素,一种从黄芫花中分离出的新型蛋白激酶C激活剂。

Daphnoretin, a new protein kinase C activator isolated from Wikstroemia indica C.A. Mey.

作者信息

Ko F N, Chang Y L, Kuo Y H, Lin Y L, Teng C M

机构信息

Pharmacological Institute, College of Medicine, National Taiwan University, Taipei.

出版信息

Biochem J. 1993 Oct 1;295 ( Pt 1)(Pt 1):321-7. doi: 10.1042/bj2950321.

Abstract

Daphnoretin, a biologically active principle isolated from Wikstroemia indica C.A. Mey., caused platelet aggregation in washed rabbit platelets, platelet-rich plasma and whole blood. The aggregation of and ATP release from platelets induced by daphnoretin were similar to phorbol ester- and diacylglycerol-induced aggregation and release. The EC50 values of daphnoretin-, phorbol 12,13-dibutyrate (PDBu)- and 1-oleoyl-2-acetylglycerol (OAG)-induced platelet aggregation in washed rabbit platelets were 17.2 +/- 2.8 microM, 20.6 +/- 2.1 nM and 38.6 +/- 1.7 microM respectively. Platelet aggregation induced by daphnoretin and PDBu was not inhibited by indomethacin, BN52021 or sodium nitroprusside. ADP-scavenging systems, apyrase and phosphocreatine/creatine kinase, showed weak inhibition of the aggregation, and EGTA, triflavin, verapamil and prostaglandin E1 markedly inhibited the aggregation. Staurosporine, a potent protein kinase C inhibitor, suppressed daphnoretin-, PDBu- and OAG-induced aggregation and ATP release in a concentration-dependent manner. The IC50 values of staurosporine on daphnoretin (50 microM)-, PDBu (100 nM)- and OAG (50 microM)-induced aggregation were 37.7 +/- 8.3, 52.2 +/- 6.3 and 42.8 +/- 8.9 nM respectively. Daphnoretin did not cause significant thromboxane B2 formation in rabbit platelets. Neither daphnoretin nor PDBu caused [3H]inositol monophosphate formation or an increase in intracellular Ca2+ concentration in myo-[3H]inositol-labelled and Fura-2-loaded platelets. Platelet cytosolic protein kinase C was activated by daphnoretin and PDBu in a concentration-dependent manner with an EC50 of 12.4 +/- 1.2 microM and 18.7 +/- 1.4 nM respectively. Membrane-associated protein kinase C activity was increased by either daphnoretin or PDBu. [3H]PDBu binding to washed rabbit platelets was inhibited by daphnoretin in a concentration-dependent manner with an IC50 value of 45.2 +/- 5.2 microM. These results indicate that daphnoretin is a protein kinase C activator in rabbit platelets.

摘要

瑞香素是从了哥王(Wikstroemia indica C.A. Mey.)中分离得到的一种生物活性成分,可引起洗涤过的兔血小板、富含血小板血浆和全血中的血小板聚集。瑞香素诱导的血小板聚集和ATP释放与佛波酯和二酰基甘油诱导的聚集和释放相似。在洗涤过的兔血小板中,瑞香素、佛波醇12,13 - 二丁酸酯(PDBu)和1 - 油酰基 - 2 - 乙酰甘油(OAG)诱导血小板聚集的EC50值分别为17.2±2.8微摩尔、20.6±2.1纳摩尔和38.6±1.7微摩尔。瑞香素和PDBu诱导的血小板聚集不受吲哚美辛、BN52021或硝普钠的抑制。ADP清除系统、腺苷三磷酸双磷酸酶和磷酸肌酸/肌酸激酶对聚集有微弱抑制作用,而乙二醇双四乙酸、三黄素、维拉帕米和前列腺素E1则显著抑制聚集。强效蛋白激酶C抑制剂星形孢菌素以浓度依赖的方式抑制瑞香素、PDBu和OAG诱导的聚集和ATP释放。星形孢菌素对瑞香素(50微摩尔)、PDBu(100纳摩尔)和OAG(50微摩尔)诱导的聚集的IC50值分别为37.7±8.3、52.2±6.3和42.8±8.9纳摩尔。瑞香素不会在兔血小板中引起显著的血栓素B2形成。瑞香素和PDBu均不会在肌醇 - [3H]标记且负载Fura - 2的血小板中引起[3H]肌醇单磷酸形成或细胞内Ca2 +浓度升高。血小板胞质蛋白激酶C被瑞香素和PDBu以浓度依赖的方式激活,EC50分别为12.4±1.2微摩尔和18.7±1.4纳摩尔。膜相关蛋白激酶C活性被瑞香素或PDBu增强。[3H]PDBu与洗涤过的兔血小板的结合被瑞香素以浓度依赖的方式抑制,IC50值为45.2±5.2微摩尔。这些结果表明瑞香素是兔血小板中的一种蛋白激酶C激活剂。

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