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低分子量肝素的药理学

Pharmacology of low molecular weight heparins.

作者信息

Harenberg J

机构信息

Department of Medicine, Faculty of Clinical Medicine, University of Heidelberg, Mannheim, FRG.

出版信息

Semin Thromb Hemost. 1990 Oct;16 Suppl:12-8.

PMID:1962899
Abstract

The investigations on LMW heparins that are reviewed in this article demonstrate that there is no relationship between the specific anti-Factor Xa activity and the release of HTGL activity after intravenous or subcutaneous administration to man. The measurement of anti-Factor Xa-like activity in patients treated with unfractionated or with LMW heparin was validated in whole blood samples obtained from the fingertip using Heptest reagents. Administration of high doses of LMW heparin twice daily resulted in a small but significant accumulation in healthy persons. The half-life of anti-Factor Xa-like activity increased after repeated administration, indicating that glycosaminoglycans or other compounds are released by LMW heparin into the bloodstream. The studies indicated that the improved pharmacologic properties may induce fewer side effects than unfractionated heparin and that patients with contraindications to unfractionated heparin or oral anticoagulants may be given long-term treatment with LMW heparin.

摘要

本文中所综述的关于低分子量肝素的研究表明,对人体进行静脉或皮下给药后,其特定的抗Xa因子活性与肝甘油三酯脂肪酶(HTGL)活性的释放之间不存在关联。使用Heptest试剂,对来自指尖的全血样本进行检测,验证了接受普通肝素或低分子量肝素治疗患者的抗Xa因子样活性。健康人每日两次大剂量给予低分子量肝素后,会出现少量但显著的蓄积。重复给药后,抗Xa因子样活性的半衰期延长,这表明低分子量肝素可将糖胺聚糖或其他化合物释放到血液中。研究表明,与普通肝素相比,低分子量肝素改善后的药理特性可能会减少副作用,并且对于普通肝素或口服抗凝剂有禁忌的患者,也可给予低分子量肝素进行长期治疗。

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