[Role of protein C in endotoxin-induced release of plasminogen activator inhibitor from endothelial cell].

K Okajima, S Koga, T Nakagaki, H Okabe, A Funatsu, K Takatsuki
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Abstract

To elucidate the role of protein C (PC) in the release of plasminogen activator inhibitor (PAI) from endothelial cells, the effect of PC and activated protein C (APC) on plasma levels of PAI in endotoxin (ET)-treated rats was examined. When activated by snake venom, human PC significantly prolonged the activated partial thromboplastin time (APTT) of both human and rat plasma samples. Addition of APC also prolonged the APTT of both human and rat plasma samples. PAI activity in plasma from septicemic patients and ET-treated rats was neutralized by APC. A small dose of ET (0.1 microgram/kg) gradually increased plasma PAI activity, which became maximum 3h after ET-treatment. APC administered prior to ET-treatment, PC decreased PAI activity, however, no such inhibition was seen when administered after ET-treatment. A significant negative correlation between PC concentrations and PAI activities was observed in plasma from septicemic patients. These findings indicated that activation of PC on endothelial surface plays a regulatory role in releasing PAI and that endotoxin might inhibit the surface activation of PC.

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[蛋白C在内毒素诱导的纤溶酶原激活物抑制剂从内皮细胞释放中的作用]。
为了阐明蛋白C (PC)在内皮细胞释放纤溶酶原激活物抑制剂(PAI)中的作用,我们观察了蛋白C和活化蛋白C (APC)对内毒素(ET)处理大鼠血浆PAI水平的影响。当被蛇毒激活时,人PC显著延长了人和大鼠血浆样品的活化部分凝血活素时间(APTT)。APC的加入也延长了人和大鼠血浆样品的APTT。APC可中和败血症患者和et治疗大鼠血浆中的PAI活性。小剂量ET(0.1微克/千克)逐渐使血浆PAI活性升高,并在ET处理后3h达到最大值。在et治疗前施用APC, PC降低了PAI活性,但在et治疗后施用APC,没有发现这种抑制作用。败血症患者血浆中PC浓度与PAI活性呈显著负相关。提示内皮细胞表面PC的活化对PAI的释放具有调节作用,内毒素可能抑制了PC的表面活化。
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