Why the study?
Do various antithrombotic agents, thrombocytopenia, and flow modifications affect time to occlusion and thrombus weight in a rat model of FeCl3-induced thrombosis?
Do various antithrombotic agents, thrombocytopenia, and flow modifications affect time to occlusion and thrombus weight in a rat model of FeCl3-induced thrombosis?
The study demonstrates the flow and platelet dependency of the FeCl3-induced thrombosis model in rats, supporting its physiological relevance for thrombosis research.
Supports FeCl3 rat model validity for thrombosis research; leaves open clinical translation and human applicability.
Further to characterize the processes involved in the FeCl3-induced thrombosis model, we determined the effect of aspirin, heparin, hirudin, trans-4-(aminomethyl) cyclohexane carboxylic acid (AMCHA), thrombocytopenia, and flow modifications on time to occlusion (TTO) and thrombus weight (TW) in the rat carotid artery. Aspirin, from 3 to 100 mg/kg, showed no dose-response relation for either TTO or TW and did not significantly affect ex vivo platelet aggregation. Heparin, at doses that significantly increased the activated partial thromboplastin time (APTT), dose-dependently increased the TTO of animals that showed an occlusion during the monitoring period and also reduced the TW. Hirudin required constant infusion to prevent occlusion and reduce the TW, when the APTT was also significantly increased. AMCHA did not affect the TW but reduced the TTO. Animals made thrombocytopenic by the use of antiplatelet serum did not occlude during the monitoring period, and the TW was significantly reduced. Changes in flow showed that the TTO was not affected, but the TW showed an inverse correlation with average flow. The results obtained for platelet depletion and flow modifications expand on previous findings with this model and support the physiological relevance of the model.
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Lockyer et al. (1999) studied this question.
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