Key result
FUT-175 at doses of 0.01 or 0.1 mg/kg reduced the extent of changes in coagulation parameters caused by endotoxin-induced disseminated intravascular coagulation in rats.
Why the study?
Does FUT-175 improve coagulation parameters and reduce renal fibrin thrombi in a rat model of endotoxin-induced DIC?
Does FUT-175 improve coagulation parameters and reduce renal fibrin thrombi in a rat model of endotoxin-induced DIC?
FUT-175, a synthetic protease inhibitor, mitigates coagulation abnormalities and renal microthrombosis in a rat model of endotoxin-induced DIC.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for FUT-175 in rat endotoxin-induced DIC; human trials required before any clinical consideration.
The effects of FUT-175 (6-amidino-2-naphthyl-4-guanidino benzoate-dimethanesulfonate), a new synthetic protease inhibitor, on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats. Experimental DIC was induced by a 4-hour sustained infusion of endotoxin at a dose of 100 mg/kg. The rats were infused continuously with FUT-175 at 0.001, 0.01, 0.1, 1.0 or 10.0 mg/kg into a femoral vein for 4 h. Simultaneously with the agent infusion, endotoxin (100 mg/kg/4 h) was administered into the contralateral femoral vein. A protective effect against DIC was noted in the rats treated with 0.01 or 0.1 mg/kg of FUT-175 in the following parameters: fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count and the number of renal glomeruli with fibrin thrombi. These results demonstrated that FUT-175 reduces the extent of changes of the coagulation parameters caused by DIC.
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Yoshikawa et al. (2009) studied Endotoxin-induced disseminated intravascular coagulation (DIC). FUT-175 was evaluated on Coagulation parameters (fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count, renal glomeruli with fibrin thrombi). FUT-175 at doses of 0.01 or 0.1 mg/kg reduced the extent of changes in coagulation parameters caused by endotoxin-induced disseminated intravascular coagulation in rats.
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