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静脉输注去氨加压素后体内的纤溶酶原激活。采用基于新型单克隆抗体的放射免疫分析法对纤溶酶-α2-抗纤溶酶复合物进行定量评估。

Plasminogen activation in vivo upon intravenous infusion of DDAVP. Quantitative assessment of plasmin-alpha 2-antiplasmin complex with a novel monoclonal antibody based radioimmunoassay.

作者信息

Levi M, de Boer J P, Roem D, ten Cate J W, Hack C E

机构信息

Center for Thrombosis, Haemostasis and Atherosclerosis Research, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Thromb Haemost. 1992 Jan 23;67(1):111-6.

PMID:1377412
Abstract

Infusion of desamino-d-arginine vasopressin (DDAVP) results in an increase in plasma plasminogen activator activity. Whether this increase results in the generation of plasmin in vivo has never been established. A novel sensitive radioimmunoassay (RIA) for the measurement of the complex between plasmin and its main inhibitor alpha 2-antiplasmin (PAP complex) was developed using monoclonal antibodies preferentially reacting with complexed and inactivated alpha 2-antiplasmin and monoclonal antibodies against plasmin. The assay was validated in healthy volunteers and in patients with an activated fibrinolytic system. Infusion of DDAVP in a randomized placebo controlled crossover study resulted in all volunteers in a 6.6-fold increase in PAP complex, which was maximal between 15 and 30 min after the start of the infusion. Hereafter, plasma levels of PAP complex decreased with an apparent half-life of disappearance of about 120 min. Infusion of DDAVP did not induce generation of thrombin, as measured by plasma levels of prothrombin fragment F1+2 and thrombin-antithrombin III (TAT) complex. We conclude that the increase in plasminogen activator activity upon the infusion of DDAVP results in the in vivo generation of plasmin, in the absence of coagulation activation. Studying the DDAVP induced increase in PAP complex of patients with thromboembolic disease and a defective plasminogen activator response upon DDAVP may provide more insight into the role of the fibrinolytic system in the pathogenesis of thrombosis.

摘要

输注去氨基 - D - 精氨酸血管加压素(DDAVP)会导致血浆纤溶酶原激活物活性增加。这种增加是否会在体内导致纤溶酶的生成尚未得到证实。我们开发了一种新型的灵敏放射免疫测定法(RIA),用于测量纤溶酶与其主要抑制剂α2 - 抗纤溶酶之间的复合物(PAP复合物),该方法使用了优先与复合且失活的α2 - 抗纤溶酶反应的单克隆抗体以及抗纤溶酶的单克隆抗体。该测定法在健康志愿者和纤维蛋白溶解系统激活的患者中进行了验证。在一项随机安慰剂对照交叉研究中,对志愿者输注DDAVP后,所有志愿者的PAP复合物增加了6.6倍,在输注开始后15至30分钟达到最大值。此后,PAP复合物的血浆水平下降,其表观消失半衰期约为120分钟。通过凝血酶原片段F1 + 2和凝血酶 - 抗凝血酶III(TAT)复合物的血浆水平测量发现,输注DDAVP并未诱导凝血酶的生成。我们得出结论,输注DDAVP后纤溶酶原激活物活性的增加会在不激活凝血的情况下导致体内纤溶酶的生成。研究血栓栓塞性疾病患者中DDAVP诱导的PAP复合物增加以及DDAVP作用下纤溶酶原激活物反应缺陷,可能会为纤维蛋白溶解系统在血栓形成发病机制中的作用提供更多见解。

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