Thromb Haemost 1996; 76(04): 621-626
DOI: 10.1055/s-0038-1650632
Original Article
Schattauer GmbH Stuttgart

Antithrombotic Effect of Human Recombinant Tissue Factor Pathway Inhibitor on Endotoxin-induced Intravascular Coagulation in Rats: Concerted Effect with Antithrombin

Yu-ichi Kamikubo
The Chemo-Sero-Therapeutic Research Institute, Kumamoto, Japan
,
Tsutomu Hamuro
The Chemo-Sero-Therapeutic Research Institute, Kumamoto, Japan
,
Jun-ichi Matsuda
The Chemo-Sero-Therapeutic Research Institute, Kumamoto, Japan
,
Noriko Shinya
The Chemo-Sero-Therapeutic Research Institute, Kumamoto, Japan
,
Seiji Miyamoto
The Chemo-Sero-Therapeutic Research Institute, Kumamoto, Japan
,
Akinobu Funatsu
The Chemo-Sero-Therapeutic Research Institute, Kumamoto, Japan
,
Hisao Kato
1   National Cardiovascular Center Research Institute, Osaka, Japan
› Author Affiliations
Further Information

Publication History

Received 25 March 1996

Accepted after resubmission 13 June 1996

Publication Date:
10 July 2018 (online)

Summary

In our current study, we examined the antithrombotic effect of Chinese hamster ovary cell-derived human recombinant tissue factor pathway inhibitor (h-rTFPI) by intravenous injection of h-rTFPI with or without antithrombin into endotoxin-treated rats. An injection of h-rTFPI at a high dose (4 mg/kg of h-rTFPI or three doses of 1 mg/kg) significantly prevented the decrease of fibrinogen and factor VIII and the increase of fibrin/fibrinogen degradation products and glutamic-pyruvic transaminase in rats, while a single injection of 1 mg/kg of h-rTFPI or 250 U/kg of antithrombin did not significantly prevent intravascular coagulation. However, a simultaneous injection of 1 mg/kg of h-rTFPI and 250 U/kg of antithrombin did significantly prevent intravascular coagulation. From the studies on the clearance rate and immunohistochemical staining of injected h-rTFPI into normal rats, we found that most of the intravenously-injected h-rTFPI was localized on the central vein and sinusoids in the liver and catabolized via the proteoglycan-mediated pathway with a half-life of 48 min. These results suggest that h-rTFPI and antithrombin prevented endotoxin-induced intravascular coagulation in concert by binding to the vascular walls of the liver and by inhibiting fibrin formation on Kupffer cells in hepatic sinusoids.

 
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