Heyns A D, Lötter M G, Badenhorst P N, Kotze H, Killian F C, Herbst C, van Reenen O R, Minnaar P C
Thromb Haemost. 1980 Oct 31;44(2):65-8.
The pathogenesis of thrombocytopenia induced by intravenous protamine sulphate was studied in six patients who underwent cardiopulmonary bypass surgery, and in three normal volunteers. Autologous platelets were labelled with (111)Indium-oxine. Platelet lifespan was determined. In vivo (111)In-platelet localization, organ redistribution and sites of destruction were quantitated with a scintillation camera and a computer-assisted imaging system. Protamine induced a transient thrombocytopenia, maximal 5-10 min after injection, and 30-40 min in duration. . The thrombocytopenia was accompanied by a transient accumulation of platelets in the liver. The splenic platelet pool remained unaltered and no platelets accumulated in the lungs. Platelet survival, measured in two volunteers, was slightly longer than normal and fitted a linear function best. There was a severe transient neutropenia during the period of thrombocytopenia. We conclude that protamine-induced thrombocytopenia is caused by hepatic accumulation of "activated" platelets or platelet aggregates, the process is reversible, and in the two normal volunteers studied, platelet survival was not affected.
对6例接受体外循环手术的患者及3名正常志愿者,研究了静脉注射硫酸鱼精蛋白所致血小板减少症的发病机制。用(111)铟-氧喹啉标记自体血小板,测定血小板寿命。用闪烁相机和计算机辅助成像系统对体内(111)铟标记血小板的定位、器官再分布及破坏部位进行定量分析。鱼精蛋白引起短暂性血小板减少,注射后5 - 10分钟达峰值,持续30 - 40分钟。血小板减少伴有肝脏内血小板短暂性积聚。脾内血小板池保持不变,肺内无血小板积聚。在两名志愿者中测得的血小板存活时间略长于正常,且最符合线性函数。血小板减少期间出现严重短暂性中性粒细胞减少。我们得出结论,鱼精蛋白诱导的血小板减少是由“活化”血小板或血小板聚集体在肝脏的积聚所致,该过程是可逆的,且在所研究的两名正常志愿者中,血小板存活未受影响。