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机构地区:[1]同济医科大学药理教研室
出 处:《药学学报》1997年第1期1-4,共4页Acta Pharmaceutica Sinica
摘 要:用比浊法和放射免疫分析技术研究甲基莲心碱(Nef)抗血小板聚集作用及其对TXA2/PGI2与cAMP/cGMP浓度的影响。结果显示,Nef在体外明显抑制ADP,胶原,AA及PAF诱导的家兔血小板聚集,IC50分别为16,22,193及103μmol·L-1;Nef明显抑制AA诱导的血小板TXA2的生成和释放,对动脉环PGI2的生成有促进作用;Nef剂量依赖性地升高血小板cAMP浓度,对cGMP无明显影响。结果提示Nef抗血小板聚集作用的机理与抑制TXA2生成,增加血管PGI2及血小板cAMP含量有关。Neferine (Nef), a hypotensive agent with antiarrythmic action, is a dibenzyl isoquinoline alkaloid isolated from a Chinese medicinal herb( Nelumbo nucifera Gaertn). Its effects on platelet aggregation and TXA 2/PGI 2 and cAMP/cGMP balance were studied with methods of turbidimetry and RIA. Nef was shown to significantly inhibit rabbit platelet aggregation induced by ADP, collagen, arachidonic acid (AA) and platelet-activating factor(PAF) with IC 50 of 16, 22, 193 and 103 μmol·L -1 , respectively. Nef was found to increase vascular 6 keto PGF 1α and platelet cAMP levels in dose dependent manner, but inhibit AA stimulated TXA 2 release from platelets. Nef showed no significant effect on the platelet cGMP level. The results suggest that the mechanism of Nef on platelet aggregation is related to regulation of TXA 2/PGI 2 and cAMP/cGMP balance.
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