首页> 外文期刊>Phytomedicine : >Inhibition of platelet activating factor (PAF)-induced aggregation of human thrombocytes by ginkgolides: considerations on possible bleeding complications after oral intake of Ginkgo biloba extracts.
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Inhibition of platelet activating factor (PAF)-induced aggregation of human thrombocytes by ginkgolides: considerations on possible bleeding complications after oral intake of Ginkgo biloba extracts.

机译:银杏内酯抑制血小板活化因子(PAF)诱导的人类血小板聚集:口服银杏叶提取物后可能的出血并发症的考虑。

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摘要

The special Ginkgo biloba leaf extract EGb 761 is marketed for more then two decades. During this time its therapeutic efficacy and favorable safety profile have been proven in numerous clinical trails as well as by postmarketing surveillance in accordance with German drug regulations. During recent years, however, several cases of hemorrhage have been reported to occur in coincidence with the use of Ginkgo products. Although a clear causality between Ginkgo intake and bleeding could not be established, these observations have generally been explained by the platelet-activating factor (PAF)-antagonistic action of ginkgolides, which represent characteristic constituents of Ginkgo extracts. PAF was originally characterized by inducing aggregation and secretion of serotonin and histamine from rabbit platelets. We now confirmed that induction of aggregation of human platelets by PAF requires at least 200 times higher concentration when compared to rabbit cells. Under the chosen experimental conditions, PAF-mediated aggregation of human platelets was half-maximally inhibited by ginkgolide B, A, C and J at concentrations of 2.5, 15.8, 29.8 and 43.5 microg/ml, respectively. These concentrations are generally more than 100 times higher as the peak plasma values measured after oral intake of EGb 761 at recommended doses between 120 and 240 mg. As PAF is a 'weak' platelet activator, which does not appear to be of importance for primary hemostasis, our results rise serious doubts that the PAF antagonistic effect of ginkgolides could be responsible for hemorrhage in patients taking EGb 761.
机译:特殊的银杏叶提取物EGb 761的上市时间超过了二十年。在这段时间里,它的治疗功效和良好的安全性已在众多临床试验以及根据德国药品法规进行的上市后监测中得到证明。然而,近年来,已经报道了一些与使用银杏产品同时发生的出血事件。尽管无法确定银杏摄入量与出血之间的明确因果关系,但这些观察结果通常由银杏内酯的血小板活化因子(PAF)拮抗作用解释,银杏内酯代表银杏提取物的特征成分。 PAF最初的特征是诱导兔血小板中血清素和组胺的聚集和分泌。现在我们证实,与兔细胞相比,PAF诱导人血小板聚集至少需要200倍以上的浓度。在所选的实验条件下,银杏内酯B,A,C和J分别以2.5、15.8、29.8和43.5 microg / ml的浓度将PAF介导的人类血小板聚集抑制了一半。这些浓度通常是在120至240 mg的推荐剂量口服EGb 761后测得的血浆峰值峰值的100倍以上。由于PAF是一种“弱”血小板活化剂,似乎对原发性止血作用并不重要,因此我们的结果引起了人们的严重怀疑,即银杏内酯的PAF拮抗作用可能是导致服用EGb 761的患者出血的原因。

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