首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Desmopressin (DDAVP) acts on platelets to generate platelet microparticles and enhanced procoagulant activity.
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Desmopressin (DDAVP) acts on platelets to generate platelet microparticles and enhanced procoagulant activity.

机译:去氨加压素(DDAVP)作用于血小板以产生血小板微粒并增强促凝活性。

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摘要

Desmopressin (DDAVP), an analog of vasopressin (AVP), has wide clinical application as an anti-hemorrhagic (AH) agent. DDAVP in vivo releases vWF from endothelial cells but is reported to have little action on platelets. However, DDAVP is often used to improve hemostasis in platelet dysfunctions. We examined the effect of DDAVP on platelet microparticle (PMP) formation and procoagulant activity in vitro using platelets from normal volunteers and in vivo in six patients receiving DDAVP therapy. In the former, platelets were incubated with DDAVP (0.5 to 25 nM) and PMP released were stained with FITC-labeled MAb alpha-GP IIb/IIIa for flow cytometry. Procoagulant activity was measured in a clot-based assay using Russel's viper venom (RVV) calibrated with cephalin. A mean increase of 2-3 fold was observed in both PMP and procoagulant activity. Parallel to these observations was a dose-dependent rise in organelle-associated Ca2+. The assays were also performed on six patients prior to and at one hour after infusion of DDAVP, and similar but lesser effects were observed. We conclude that DDAVP acts on platelets in vitro, and that these effects may contribute to the hemostatic action of DDAVP in platelet dysfunctions in vivo.
机译:去氨加压素(DDAVP)是血管加压素(AVP)的类似物,作为抗出血(AH)剂具有广泛的临床应用。 DDAVP在体内从内皮细胞释放vWF,但据报道对血小板几乎没有作用。但是,DDAVP通常用于改善血小板功能障碍的止血作用。我们使用六名接受DDAVP治疗的患者使用正常志愿者的血小板和体内检测了DDAVP对血小板微粒(PMP)形成和促凝活性的影响。在前者中,将血小板与DDAVP(0.5至25 nM)孵育,并将释放的PMP用FITC标记的MAb alpha-GP IIb / IIIa染色,以进行流式细胞术。促凝活性是在基于凝块的测定中进行的,该测定使用已用脑苷校正的罗素毒蛇毒(RVV)。在PMP和促凝活性上均观察到2-3倍的平均增加。与这些观察结果平行的是细胞器相关的Ca2 +呈剂量依赖性上升。还在DDAVP输注之前和之后的一小时内对六名患者进行了测定,观察​​到了相似但较少的影响。我们得出结论,DDAVP在体外作用于血小板,并且这些作用可能有助于DDAVP在体内血小板功能障碍中的止血作用。

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