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普通肝素和低分子量肝素对血浆中凝血酶生成的作用方式。

Mode of action of unfractionated and low molecular weight heparins on the generation of thrombin in plasma.

作者信息

Hemker H C, Béguin S

机构信息

Department of Biochemistry, University of Limburg, Maastricht, The Netherlands.

出版信息

Haemostasis. 1990;20 Suppl 1:81-92. doi: 10.1159/000216164.

Abstract

Heparins, unfractionated and low molecular weight, act primarily by their scavenging of thrombin (S-type heparins). Via the feedback effect on factor VIII this has a secondary effect on prothrombin conversion in the intrinsic pathway (activated partial thromboplastin time). The anti-Xa action of a heparin will not significantly inhibit prothrombin conversion, except in the case of ultra low molecular weight heparins (P-type heparins) that have no significant antithrombin activity. These P-type heparins need, therefore, be given at high doses to have an antithrombotic effect. In platelet-rich plasma heparins retard platelet activation by lowering thrombin levels. Activated platelets neutralize up to 0.5 U/ml of unfractionated heparin, but low molecular weight heparin is much less affected.

摘要

普通肝素和低分子肝素主要通过清除凝血酶(S型肝素)发挥作用。通过对因子VIII的反馈作用,这对内源性途径中凝血酶原的转化(活化部分凝血活酶时间)有次要影响。肝素的抗Xa作用不会显著抑制凝血酶原转化,除非是没有显著抗凝血酶活性的超低分子肝素(P型肝素)。因此,这些P型肝素需要高剂量给药才能产生抗血栓作用。在富含血小板的血浆中,肝素通过降低凝血酶水平来延缓血小板活化。活化的血小板可中和高达0.5 U/ml的普通肝素,但低分子肝素受影响小得多。

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