Thromb Haemost 2003; 90(03): 414-421
DOI: 10.1160/TH02-09-0104
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Activated thrombin-activatable fibrinolysis inhibitor attenuates spontaneous fibrinolysis of batroxobin-induced fibrin deposition in rat lungs

Chengliang Wu
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
2   Jiangsu Institute of Hematology, Suzhou University, Suzhou, P.R. China
,
Ningzheng Dong
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
2   Jiangsu Institute of Hematology, Suzhou University, Suzhou, P.R. China
,
Valdeci da Cunha
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
,
Baby Martin-McNulty
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
,
Katherine Tran
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
,
Mariko Nagashima
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
,
Qingyu Wu
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
,
John Morser
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
,
Yi-Xin Wang
1   Departments of Cardiovascular Research and Pharmacology, Berlex Biosciences, Richmond, California, USA
› Author Affiliations
Further Information

Publication History

Received 20 September 2002

Accepted after resubmission 22 May 2003

Publication Date:
05 December 2017 (online)

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Summary

Studies have shown that inhibition of TAFI by small peptides enhances pharmacological effects of tPA in animal models of thrombosis, suggesting that TAFI modulates the fibrinolytic system. In this study, we investigated the effect of activated human TAFI (TAFIa) on endogenous fibrinolysis in a rat model of intravascular fibrin deposition. 125I-labeled fibrinogen was injected intravenously followed by a bolus injection of batroxo-bin, a thrombin-like enzyme. Batroxobin cleaved fibrinogen to form insoluble fibrin that was deposited in tissues, including the lungs. This was shown by a decrease of radioactivity in the blood as a result of consumption of 125I-labeled fibrinogen and an elevation of radioactivity in the lungs 5 min following batroxobin administration. Endogenous fibrinolysis was detected by a gradual increase in radioactivity in the blood and a decrease in radioactivity in the lungs at 30 min, an indication of radio-labeled fibrin degradation products (FDPs) being released into the circulation from the tissues. Intravenous administration of human TAFIa dose-dependently attenuated the later phase reduction of radioactivity in the lungs. When the dose of TAFIa was 218 μg/kg, giving a peak plasma level of TAFIa 0.9 ± 0.05 μg/ml, the spontaneous fibrinolysis was completely prevented. These results provide direct evidence that an increase in circulating TAFIa impairs endogenous clot lysis in a rat model of fibrin deposition.