Korninger C, Wagner O, Binder B R
J Lab Clin Med. 1985 Jun;105(6):718-24.
An assay system for determination of the "fast"-acting inhibitor (antiactivator, AA) of tissue-type plasminogen activator (tPA) in human plasma was developed. The system is based on incubation of plasma samples with various amounts of vessel wall-derived tPA for 8 minutes at 25 degrees C, followed by acidification and determination of the residual tPA activity by an indirect spectrophotometric assay. One unit of AA was defined as the amount inhibiting 1 U of tPA. AA levels in normal controls (n = 26) were 1.4 to 17.4 U/ml (median 3.0 U/ml) and 0.9 to 17.5 U/ml (median 3.0 U/ml) in patients with a history of deep venous thrombosis (n = 26). When plasma was subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by reverse fibrin autography, AA activity appeared as an inhibitory band corresponding to a relative molecular mass of 50,000. In six samples the inhibitory activity of this band was directly correlated to the functional AA activity of the plasma samples.
开发了一种用于测定人血浆中组织型纤溶酶原激活物(tPA)“快速”作用抑制剂(抗激活剂,AA)的检测系统。该系统基于将血浆样品与不同量的血管壁来源的tPA在25℃下孵育8分钟,然后酸化并通过间接分光光度法测定残留的tPA活性。1个AA单位定义为抑制1单位tPA的量。正常对照(n = 26)中的AA水平为1.4至17.4 U/ml(中位数3.0 U/ml),有深静脉血栓形成病史的患者(n = 26)中的AA水平为0.9至17.5 U/ml(中位数3.0 U/ml)。当血浆进行十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳,随后进行反向纤维蛋白自显影时,AA活性表现为对应于相对分子质量50,000的抑制带。在六个样品中,该带的抑制活性与血浆样品的功能性AA活性直接相关。