Thromb Haemost 2003; 89(02): 256-263
DOI: 10.1055/s-0037-1613440
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

In vivo pig models of venous thrombosis mimicking human disease

Chantal Kang
1   I.V.S. Lariboisière Teaching Hospital, Paris
,
Michel Bonneau
2   INRA, UEPSD, Jouy en Josas
,
Jean-Philippe Brouland
3   Pathology Department, Lariboisière Teaching Hospital, Paris, France
,
Claire Bal dit Sollier
1   I.V.S. Lariboisière Teaching Hospital, Paris
,
Ludovic Drouet
1   I.V.S. Lariboisière Teaching Hospital, Paris
2   INRA, UEPSD, Jouy en Josas
› Author Affiliations
Further Information

Publication History

Received 16 October 2002

Accepted after revision 21 November 2002

Publication Date:
07 December 2017 (online)

Summary

Most animal models of venous thrombosis involve acute thrombosis with hypercoagulability in small rodents. To better replicate human disease, we developed two models in the pig, a species similar to humans in size and in vascular and coagulation reactivity. One model involves de-endothelialisation with 50% or 80% stenosis and the other replacement of a venous segment by a Gore-Tex™ vascular prosthesis. Both models were tested with and without acute induced hypercoagulability (thromboplastin infusion). Thrombi obtained without thromboplastin infusion were composed of a multilayered platelet and a fibrin meshwork structure similar to that usually found in humans. With thromboplastin infusion, the thrombi were homogeneous fibrin structures imprisoning red blood cells. The high incidence of thrombosis obtained with the 80% stenosis model would be useful for studying anticoagulant treatments, whereas the low incidence with 50% stenosis would be useful for evaluating procoagulant effects of conditions or treatments. These new models shed further light on the development of venous thrombi under conditions similar to those seen in humans and may prove useful for investigating anticoagulant and procoagulant effects.

 
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