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体内鱼精蛋白氯化物对低分子量肝素的抑制作用。

Inhibition of low molecular weight heparin by protamine chloride in vivo.

作者信息

Harenberg J, Gnasso A, de Vries J X, Zimmermann R, Augustin J

出版信息

Thromb Res. 1985 Apr 1;38(1):11-20. doi: 10.1016/0049-3848(85)90003-9.

Abstract

To determine the antagonization of anticoagulant and lipolytic effects of a low molecular weight [LMW] heparin preparation protamine chloride was given intravenously after i.v. injection of LMW or normal heparin. The effects of normal heparin on factor Xa, thrombin, aPTT, lipoprotein [LPL] and hepatic triglyceride lipase [HTGL] activities were neutralized immediately by i.v. protamine. The inhibition of thrombin and aPTT by LMW heparin were also abolished, whereas the effects on LPL and HTGL were counteracted to 80% and on factor Xa only to 40% by i.v. protamine chloride. No rebound of the anticoagulant or lipolytic effect was detected. It is assumed that haemorrhagic complication during therapy can be antagonized by protamine chloride. The incomplete inhibitory effect of protamine chloride on LPL, HTGL and factor Xa activities of LMW heparin indicate that protamine chloride requires more than 14 saccharide units in the heparin molecule for interaction.

摘要

为了确定低分子量(LMW)肝素制剂抗凝和脂解作用的拮抗情况,在静脉注射LMW肝素或普通肝素后静脉注射氯化鱼精蛋白。静脉注射鱼精蛋白可立即中和普通肝素对Xa因子、凝血酶、活化部分凝血活酶时间(aPTT)、脂蛋白脂肪酶(LPL)和肝甘油三酯脂肪酶(HTGL)活性的影响。LMW肝素对凝血酶和aPTT的抑制作用也被消除,而静脉注射氯化鱼精蛋白可使LMW肝素对LPL和HTGL的作用被抵消80%,对Xa因子的作用仅被抵消40%。未检测到抗凝或脂解作用的反弹。推测治疗期间的出血并发症可用氯化鱼精蛋白拮抗。氯化鱼精蛋白对LMW肝素的LPL、HTGL和Xa因子活性的不完全抑制作用表明,肝素分子中与氯化鱼精蛋白相互作用需要超过14个糖单位。

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