前激肽释放酶
凝结
血栓形成
因子十二
医学
静脉血栓形成
发病机制
基因剔除小鼠
组织因子
免疫学
内科学
药理学
激肽释放酶
生物
受体
酶
生物化学
作者
Steven P. Grover,Nigel Mackman
标识
DOI:10.1161/atvbaha.118.312130
摘要
Activation of the intrinsic pathway of coagulation contributes to the pathogenesis of arterial and venous thrombosis. Critical insights into the involvement of intrinsic pathway factors have been derived from the study of gene-specific knockout animals and targeted inhibitors. Importantly, preclinical studies have indicated that targeting components of this pathway, including FXI (factor XI), FXII, and PKK (prekallikrein), reduces thrombosis with no significant effect on protective hemostatic pathways. This review highlights the advances made from studying the intrinsic pathway using gene-specific knockout animals and inhibitors in models of arterial and venous thrombosis. Development of inhibitors of activated FXI and FXII may reduce thrombosis with minimal increases in bleeding compared with current anticoagulant drugs.
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