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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >In vivo release of tissue-type plasminogen activator antigen from the human brachial artery.
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In vivo release of tissue-type plasminogen activator antigen from the human brachial artery.

机译:从人肱动脉体内释放组织型纤溶酶原激活剂抗原。

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The rate of secretion of t-PA from vascular endothelial cells has been proposed as a good marker of endothelial function. Our aim was to measure the rate of in vivo t-PA antigen release from the human brachial artery and not from the combined vascular pool of the upper extremity. In 10 healthy male volunteers, we have occluded the forearm by a sphygmomanometer cuff for 5-7 min in order to reduce the blood flow in the brachial artery. Arterial blood samples were taken from the cubital artery above the occlusion and from the contralateral artery that served as the control. The arterial t-PA antigen concentrations were significantly higher after forearm occlusion than in the non-occluded contralateral arteries: median 3.3 (range between first and third quartile 2.1-3.6) vs. 2.5 (2.0-3.2) ng/ml, p=0.03. The PAI-1 antigen concentrations did not change significantly: 6.9 (2.3-18.6) ng/ml in the contralateral artery vs. 5.4 (1.8-8.0) ng/ml after occlusion, p=0.09. The average forward blood flow in the distal 15 cm of the brachial artery that was measured by duplex ultrasound decreased from 107 (97-118) ml/min at baseline to 25 ml/min (19-33) ml/min during occlusion. The release rate of circulating t-PA antigen was calculated as the product of the increment in arterial t-PA concentration and the average plasma flow in the arterial segment of interest with a volume of 2 ml. The median release rate of t-PA antigen under conditions of reduced blood flow in the brachial artery was 3.3 (1.1-11.5) ng/min. We conclude that the secretion of t-PA antigen from arterial endothelium of healthy subjects is substantial, whereas the arterial wall is not an important source of PAI-1 in vivo.
机译:已经提出从血管内皮细胞分泌t-PA的速率是内皮功能的良好标志。我们的目的是测量体内t-PA抗原从人肱动脉释放的速率,而不是从上肢的合并血管池释放的速率。在10名健康的男性志愿者中,我们用血压计袖带封堵了前臂5-7分钟,以减少肱动脉中的血流。从闭塞上方的肘动脉和作为对照的对侧动脉采集动脉血样。前臂闭塞后的动脉t-PA抗原浓度显着高于未闭塞的对侧动脉:中位数3.3(介于第一和第三四分位数之间2.1-3.6)与2.5(2.0-3.2)ng / ml之间,p = 0.03 。 PAI-1抗原浓度没有明显变化:对侧动脉中6.9(2.3-18.6)ng / ml,闭塞后5.4(1.8-8.0)ng / ml,p = 0.09。通过双重超声测量,肱动脉远端15 cm处的平均正向血流从基线时的107(97-118)ml / min降低到闭塞时的25 ml / min(19-33)ml / min。循环t-PA抗原的释放速率计算为动脉t-PA浓度增加量与目标动脉节段中2 ml体积的平均血浆流量的乘积。在肱动脉血流量减少的条件下,t-PA抗原的中位释放速率为3.3(1.1-11.5)ng / min。我们得出结论,健康受试者的动脉内皮中t-PA抗原的分泌是大量的,而动脉壁并不是体内PAI-1的重要来源。

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