Sustained Inhibition of Whole-Blood Clot Procoagulant Activity by Inhibition of Thrombus-Associated Factor Xa
- 1 October 1996
- journal article
- research article
- Published by Wolters Kluwer Health in Arteriosclerosis, Thrombosis, and Vascular Biology
- Vol. 16 (10) , 1285-1291
- https://doi.org/10.1161/01.atv.16.10.1285
Abstract
Progression of arterial thrombosis partly depends on thrombus-associated thrombin and activated factor X (Xa) activity. However, whether Xa or thrombin is the most appropriate target for inhibition of recurrent thrombosis is unknown. This study was designed to determine whether inhibition of Xa results in more sustained attenuation of thrombus-associated procoagulant activity than does inhibition of thrombin. Clots prepared ex vivo from human whole blood and pathological arterial thrombi from patients were preincubated in citrated plasma containing no inhibitor, 0.5 to 1 U/mL heparin, 0.5 to 1 μmol/L hirudin, 5 to 10 μmol/L tick anticoagulant peptide (TAP), 0.15 to 3 μmol/L tissue factor pathway inhibitor (TFPI), or a combination of 1 μmol/L hirudin and 10 μmol/L TAP for 2 hours. After preincubation the clots were removed from first-stage plasma, extensively washed in phosphate-buffered saline, and added to nonanticoagulated whole blood. Clots preincubated in plasma without inhibitors induced marked activation of the coagulation system in whole blood, as characterized by greater increases in the concentration of fibrinopeptide A (FPA) over 7 minutes than in blood without added clots (1522±568 compared with 117±170 ng/mL, P <.01). Preincubation of clots with heparin or hirudin did not attenuate the increases in FPA in whole blood. In contrast, compared with incubation without an inhibitor, preincubation of clots with TAP or TFPI markedly attenuated the increases in FPA when clots were added to whole blood (551±316 and 508±208 ng/mL, respectively, P <.01). Similar results were obtained with arterial thrombi from patients. Inhibition of Xa but not of thrombin results in sustained attenuation of thrombus-associated procoagulant activity. Uninhibited thrombus-associated Xa activity may account for the increases in thrombin activity that are commonly observed in clinical trials after discontinuation of thrombin inhibitors.Keywords
This publication has 22 references indexed in Scilit:
- The Coagulation ExplosionaAnnals of the New York Academy of Sciences, 1994
- Thrombosis and Fibrinolysis in Acute Myocardial InfarctionAlcohol, Clinical and Experimental Research, 1994
- Maintenance of canine coronary artery patency following thrombolysis with front loaded plus low dose maintenance conjunctive therapy. A comparison of factor Xa versus thrombin inhibitionCardiovascular Research, 1994
- Evidence for a rebound coagulation phenomenon after cessation of a 4-hour infusion of a specific thrombin inhibitor in patients with unstable angina pectorisJournal of the American College of Cardiology, 1993
- An ELISA for tissue factor using monoclonal antibodiesBlood Coagulation & Fibrinolysis, 1992
- The Pathogenesis of Coronary Artery Disease and the Acute Coronary SyndromesNew England Journal of Medicine, 1992
- Effect of heparin on coronary arterial patency after thrombolysis with tissue plasminogen activator in acute myocardial infarctionThe American Journal of Cardiology, 1990
- Coronary angiographic ruptured atheromatous plaque as a predictor of future progression of stenosisAmerican Heart Journal, 1990
- Intracoronary thrombus: Role in coronary occlusion complicating percutaneous transluminal coronary angioplastyJournal of the American College of Cardiology, 1985
- Protection of factor Xa from neutralization by the heparin-antithrombin complex.Journal of Clinical Investigation, 1983