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1型纤溶酶原激活物抑制剂(第二部分):在溶栓治疗失败中的作用。PAI-1抵抗作为新型纤溶药物的潜在益处。

Plasminogen activator inhibitor type-1 (part two): role for failure of thrombolytic therapy. PAI-1 resistance as a potential benefit for new fibrinolytic agents.

作者信息

Huber K

机构信息

Department of Cardiology, University of Vienna-General Hospital, Währinger Gürtel 18/20, A-1090 Vienna, Austria.

出版信息

J Thromb Thrombolysis. 2001 May;11(3):195-202. doi: 10.1023/a:1011952602122.

Abstract

Rapid and sustained reperfusion of an occluded coronary artery is the goal of thrombolytic therapy in acute myocardial infarction. However, the clot-dissolving efficacy of fibrinolytic agents such as tissue-type plasminogen activator (t-PA) is limited, in vivo, in part by the action of plasminogen activator inhibitor type-1 (PAI-1). A new generation of fibrinolytic agents has been genetically engineered to have greater resistance to PAI-1 inhibition. This article reviews the pathophysiologic role of PAI-1 in failure of thrombolytic therapy and describes the advantages that PAI-1-resistance may confer upon fibrinolytic agents such as TNK-t-PA, the new fibrinolytic agent with the most powerful PAI-1 resistance.

摘要

使闭塞的冠状动脉迅速且持续再灌注是急性心肌梗死溶栓治疗的目标。然而,诸如组织型纤溶酶原激活剂(t-PA)等纤溶药物在体内溶解血栓的功效受到纤溶酶原激活剂抑制剂1型(PAI-1)作用的部分限制。新一代纤溶药物经基因工程改造后对PAI-1抑制具有更强的抗性。本文综述了PAI-1在溶栓治疗失败中的病理生理作用,并描述了PAI-1抗性可能赋予纤溶药物(如TNK-t-PA,具有最强PAI-1抗性的新型纤溶药物)的优势。

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