Effects of ZK-807834, a novel inhibitor of factor Xa, on arterial and venous thrombosis in rabbits

被引:33
作者
Abendschein, DR
Baum, PK
Martin, DJ
Vergona, R
Post, J
Rumennik, G
Sullivan, ME
Eisenberg, PR
Light, DR
机构
[1] Washington Univ, Sch Med, Div Cardiovasc, St Louis, MO 63110 USA
[2] Berlex Biosci, Richmond, CA USA
关键词
thrombosis; anticoagulants; factor Xa;
D O I
10.1097/00005344-200005000-00018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inhibition of factor Xa (FXa) may interrupt thrombus progression This study compared the antithrombotic activity of a novel FXa inhibitor, ZK-807834 [MW, 527 D; Ki (human FXa), 0.11 nM], with recombinant tick anticoagulant peptide [rTAP: MW, 6,685 D; K-i, (human FXa) = 0.28 nM], and DX-9065a [MW 445 D, K-i (human FXa), 40 nM] in rabbits with arterial thrombosis induced by electrical vascular injury. 2K-807834 also was compared with low molecular weight heparin (LMWH; MW, 5,500 Di during Venous thrombosis induced by placing a copper wire and threads in the vena cava. Inhibitors were administered as an i.v. bolus and 2-h infusion. Total dosages of ZK-807834, greater than or equal to 0.7 mu mol/kg (n = 18); rTAP, greater than or equal to 1 mu mol/kg(n = 18); or DX-9065a, greater than or equal to 11 mu mol/kg(n = 18) decreased the incidence of arterial thrombotic occlusion compared with control animals (p < 0.05). However, five of six animals given the lowest effective dosage of rTAP and four of six animals given DX-9065a bled from a surgical incision >5 min, but only two of dr animals given ZK-807834 bred >5 min. Venous clot weights were reduced compared with controls for dosages of ZK-807834 greater than or equal to 0.007 mu mol/kg (n = 36) or LMWH greater than or equal to 0.2 mu mol/kg (n = 18). Prothrombin time (PT) and activated partial thromboplastin time (aPTT) were unchanged from baseline at the minimally effective dose of 2R-807834, whereas aPTT was increased twofold at the effective dose of LMWH. Thus ZK-807834 may he useful to attenuate thrombosis at lower dosages and with less perturbation of systemic hemostasis compared with available agents.
引用
收藏
页码:796 / 805
页数:10
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