Key result
Oversulfated heparin by-products activate kallikrein and thrombin via contact system stimulation.
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Thrombin generation is thought to be mediated predominantly by the tissue factor or ''extrinsic'' coagulation pathway. An alternate pathway to thrombin generation (the ''intrinsic'' pathway or contact system) has been observed when blood or plasma comes in contact with artificial surfaces. Here we present evidence for a new route to thrombin formation that begins with the activation of the contact system protein prekallikrein by oversulfated heparin (OS-HB). Kallikrein, instead of activated factor X, cleaves prothrombin to form thrombin. Thrombin then cleaves fibrinogen to form fibrin clots. Moreover, we show that OS-HB by-products induce kallikrein- and thrombin-like activities in normal human plasma and in human plasma devoid of coagulation factor X or downstream contact system components factor IX or factor XI. Oversulfated heparin by-product-induced thrombin generation may have had a role in the adverse reactions associated with the recent clinical use of contaminated heparin.
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Qian et al. (2010) studied Adverse reactions associated with contaminated heparin / coagulation pathway activation. Oversulfated heparin by-products (OS-HB) was evaluated on Thrombin generation and kallikrein-like activity. Oversulfated heparin by-products induced kallikrein- and thrombin-like activities in normal human plasma and plasma devoid of factor X, IX, or XI via contact system prekallikrein activation.
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