Yang X, Disa J, Rao A K
Thrombosis Research Center, Temple University Health Sciences Center, Philadelphia, PA 19140.
Thromb Res. 1990 Sep 1;59(5):809-18. doi: 10.1016/0049-3848(90)90394-r.
Intravenous infusion of 1-desamino-8-D-arginine vasopressin (DDAVP), an analog of arginine vasopressin (AVP), results in a rise in plasma levels of factor VIII coagulant activity and the von Willebrand factor. DDAVP infusion has been shown to shorten the prolonged bleeding time of patients with inherited platelet defects but the mechanism for this has not been fully clarified. There is little information available on the direct effect of DDAVP on platelets. We examined the effect of DDAVP on platelet responses, including Ca2+ mobilization, to understand the mechanisms by which DDAVP shortens the bleeding time in patients with primary platelet defects. In normal human platelets, DDAVP alone upto 100 microM did not induce aggregation, secretion or a rise in the intracellular Ca2+ concentration, monitored using quin2. In contrast AVP induced all three responses in a dose dependent manner. Interestingly preincubation of platelets with DDAVP at a 100-fold greater concentration inhibited the responses to AVP indicating that DDAVP does interact with the platelets. Moreover, DDAVP did not either potentiate or inhibit the responses to thrombin or ADP. These studies indicate that it is unlikely that the beneficial effect of DDAVP in patients with primary platelet defects is related to a direct stimulatory effect on platelets.
静脉输注精氨酸加压素(AVP)的类似物1-去氨基-8-D-精氨酸加压素(DDAVP)会导致血浆中凝血因子VIII促凝活性和血管性血友病因子水平升高。已证明输注DDAVP可缩短遗传性血小板缺陷患者延长的出血时间,但其机制尚未完全阐明。关于DDAVP对血小板的直接作用的信息很少。我们研究了DDAVP对血小板反应的影响,包括钙离子动员,以了解DDAVP缩短原发性血小板缺陷患者出血时间的机制。在正常人血小板中,高达100微摩尔的DDAVP单独使用不会诱导聚集、分泌或细胞内钙离子浓度升高,使用喹啉2监测。相比之下,AVP以剂量依赖的方式诱导了所有三种反应。有趣的是,用浓度高100倍的DDAVP预孵育血小板会抑制对AVP的反应,表明DDAVP确实与血小板相互作用。此外,DDAVP既不增强也不抑制对凝血酶或ADP的反应。这些研究表明,DDAVP对原发性血小板缺陷患者的有益作用不太可能与对血小板的直接刺激作用有关。