Juhan-Vague I, Alessi M C, Aillaud M F
Ann Biol Clin (Paris). 1987;45(2):202-6.
Plasminogen Activator Inhibitors (PA Inhibitor) have recently been identified in plasma. They are directed against t-PA and Urokinase. Two PA Inhibitors have been described: PA Inhibitor 1 from endothelial cells, hepatocytes and platelets and PA Inhibitor 2 from placenta. Enzymatic assays have been developed. They show that plasma levels of PA Inhibitor are very low under normal conditions, but a considerable increase (X10 or 20) is found in several pathological conditions (thrombo embolic disease, atherosclerosis, thrombotic risk factors (obesity, hypertriglyceridemia, diabetes) inflammatory syndrome, post operative period for PA Inhibitor 1, and in some physiological conditions (pregnancy for PA Inhibitor 2). These results plead for a pathogenic role of PA Inhibitor 1 in the development of thrombosis. Pharmacological products able to decrease the plasma level of PA Inhibitor are as yet scarce. Stanozolol, an anabolic steroid, some biguanides such as Metformin possess this property.
纤溶酶原激活物抑制剂(PA抑制剂)最近在血浆中被发现。它们作用于组织型纤溶酶原激活物(t-PA)和尿激酶。已描述了两种PA抑制剂:来自内皮细胞、肝细胞和血小板的PA抑制剂1以及来自胎盘的PA抑制剂2。已经开发出酶学检测方法。这些方法表明,在正常情况下,PA抑制剂的血浆水平非常低,但在几种病理状态(血栓栓塞性疾病、动脉粥样硬化、血栓形成危险因素(肥胖、高甘油三酯血症、糖尿病)、炎症综合征、PA抑制剂1的术后阶段)以及一些生理状态(PA抑制剂2在孕期)下,其水平会显著升高(升高10倍或20倍)。这些结果表明PA抑制剂1在血栓形成过程中具有致病作用。目前能够降低PA抑制剂血浆水平的药物很少。司坦唑醇,一种合成代谢类固醇,以及一些双胍类药物如二甲双胍具有这种特性。