Mannucci P M, Aberg M, Nilsson I M, Robertson B
Br J Haematol. 1975 May;30(1):81-93. doi: 10.1111/j.1365-2141.1975.tb00521.x.
Adrenaline, nicotinic acid (NA), vasopressin (LVP) and other drugs affecting vascular motility are known to increase plasminogen activator (PA) and factor-VIII plasma levels in man. To evaluate the hypothesis that NA, LVP and adrenaline release PA from the endothelial cells of the vessel wall through their common effect on vascular motility, PA has been characterized by means of a histochemical technique on vein biopsies obtained from human volunteers after infusion of the compounds. Furthermore, the effect of single and repeated administration has been compared in order to investigate whether the pattern of PA and factor-VIII variations in plasma is similar with the three drugs. There was no major difference in the PA content of the veins following the marked and sustained increase of the corresponding plasma activities. A simple explanation is that the intensity and duration of the stimulus may not be sufficient to deplete the large stores of the vessel walls. The magnitude, time course and duration of the plasmatic response after single and repeated infusions was on the whole different and peculiar for each drug. A derivative of LVP which is free of vasoactive actions was more effective than LVP in inducing the responses, which could also be elicited in two anephric subjects. These findings suggest that vasoactivity is unlikely to provide the clue to a common pathway for the fibrinolysis and coagulation response after the compounds, and support the existence of different specific receptors.
已知肾上腺素、烟酸(NA)、血管加压素(LVP)和其他影响血管运动的药物可提高人体血浆中纤溶酶原激活物(PA)和因子VIII的水平。为了评估NA、LVP和肾上腺素通过对血管运动的共同作用从血管壁内皮细胞释放PA这一假说,在向人类志愿者输注这些化合物后,通过组织化学技术对取自静脉活检组织的PA进行了特性分析。此外,还比较了单次给药和重复给药的效果,以研究这三种药物使血浆中PA和因子VIII变化的模式是否相似。在相应血浆活性显著且持续升高后,静脉中的PA含量没有重大差异。一个简单的解释是,刺激的强度和持续时间可能不足以耗尽血管壁中的大量储备。单次和重复输注后血浆反应的幅度、时间进程和持续时间总体上各不相同,且每种药物都有其独特之处。一种无血管活性作用的LVP衍生物在诱导反应方面比LVP更有效,这种反应在两名无肾受试者中也能引发。这些发现表明,血管活性不太可能为这些化合物作用后纤溶和凝血反应的共同途径提供线索,并支持存在不同的特异性受体。