Contribution of in vivo models of thrombosis to the discovery and development of novel antithrombotic agents

• Published in: Journal of pharmacological and toxicological methods Vol. 43; no. 2; pp. 101 - 116
• Main Authors: Leadley, Robert J., Chi, Liguo, Rebello, Sam S., Gagnon, Alison
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.2000
• Subjects: Animal models; Animals; Anti-thrombotics; Disease Models, Animal; Factor Xa; Factor Xa Inhibitors; Fibrinolytic Agents - therapeutic use; Hemostasis; Humans; In vivo; Mice; Mice, Knockout; Species Specificity; Thrombosis; Thrombosis - etiology; In vivo; Factor Xa; Animal models; Anti-thrombotics; Thrombosis
• ISSN: 1056-8719; 1873-488X
• DOI: 10.1016/S1056-8719(00)00095-2

Cardiovascular and cerebrovascular diseases continue to be the leading cause of death throughout the world. Over the past two decades, great advances have been made in the pharmacological treatment and prevention of thrombotic disorders (e.g., tissue plasminogen activators, platelet GPIIb/IIIa antagonists, ADP receptor antagonists such as clopidogrel, low-molecular weight heparins, and direct thrombin inhibitors). New research is leading to the next generation of antithrombotic compounds such as direct coagulation FVIIa inhibitors, tissue factor pathway inhibitors, gene therapy, and orally active direct thrombin inhibitors and coagulation Factor Xa (FXa) inhibitors. Animal models of thrombosis have played a crucial role in discovering and validiting novel drug targets, selecting new agents for clinical evaluation, and providing dosing and safety information for clinical trials. In addition, these models have provided valuable information regarding the mechanisms of these new agents and the interactions between antithrombotic agents that work by different mechanisms. This review briefly presents the pivitol preclinical studies that led to the development of drugs that have proven to be effective clinicallly. The role that animal models of thrombosis are playing in the discovery and development of novel antithrombotic agents is also described, with specific emphasis on FXa inhibitors. The major issues regarding the use of animal models of thrombosis, such as the use of positive controls, appropriate pharmacodynamic markers of activity, safety evaluation, species-specificity, and pharmacokinetics, are highlighted. Finally, the use of genetic models in thrombosis/hemostasis research and pharmacology is presented using gene-therapy for hemophilia as an example of how animal models have aided in the development of these therapies that are now being evaluated clinically. In summary, animal models have contributed greatly to the discovery of currently available antithrombotic agents and will play a primary role in the discovery and characterization of the novel antithrombotic agents that will provide safe and effective pharmacological treatment for life-threatening thrombotic diseases.