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三磷酸二腺苷(Ap3A)在肝素化富血小板血浆中高效诱导人血小板聚集。

Highly efficient induction of human platelet aggregation in heparinized platelet-rich plasma by diadenosine triphosphate (Ap3A).

作者信息

Lüthje J, Baringer J, Ogilvie A

出版信息

Thromb Haemost. 1985 Aug 30;54(2):469-71.

PMID:4082083
Abstract

Diadenosine triphosphate (Ap3A), which is a releasable dinucleotide of human platelets, induces platelet aggregation when added to heparinized platelet-rich plasma. The concentration dependence of the dinucleotide is similar to ADP. This finding is fully compatible with our recent report of the low potency of Ap3A in citrated platelet-rich plasma relative to ADP. The aggregatory effect of Ap3A in heparinized versus citrated plasma is reflected in the corresponding rates of Ap3A degradation. In citrated plasma, the hydrolysis of Ap3A is drastically slowed down because the hydrolase needs divalent metal ions. The results strongly support the assumption that the aggregatory effect of Ap3A is mediated by the enzymatic hydrolysis of Ap3A which generates ADP as the ultimate stimulus.

摘要

三磷酸二腺苷(Ap3A)是人类血小板中一种可释放的二核苷酸,当添加到肝素化富血小板血浆中时可诱导血小板聚集。该二核苷酸的浓度依赖性与ADP相似。这一发现与我们最近关于相对于ADP,Ap3A在枸橼酸化富血小板血浆中效力较低的报告完全相符。Ap3A在肝素化血浆与枸橼酸化血浆中的聚集作用反映在相应的Ap3A降解速率上。在枸橼酸化血浆中,Ap3A的水解急剧减慢,因为水解酶需要二价金属离子。这些结果有力地支持了这样一种假设,即Ap3A的聚集作用是由Ap3A的酶促水解介导的,该水解产生ADP作为最终刺激物。

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