Combined antithrombin III and C1-esterase inhibitor treatment decreases intravascular fibrin deposition and attenuates cardiorespiratory impairment in rabbits exposed to Escherichia coli endotoxin
R. Giebler et al., Combined antithrombin III and C1-esterase inhibitor treatment decreases intravascular fibrin deposition and attenuates cardiorespiratory impairment in rabbits exposed to Escherichia coli endotoxin, CRIT CARE M, 27(3), 1999, pp. 597-604
Objective: To assess the effect of a combined antithrombin III and C1-ester
ase inhibitor treatment on intravascular organ fibrin deposition and cardio
respiratory changes following intravenous Escherichia coil endotoxin (lipop
olysaccharide [LPS] 80 mu g/kg iv) exposure.
Design: Prospective, randomized trial.
Setting: Research laboratory of a university medical center.
Subjects: Anesthetized, instrumented and mechanically ventilated rabbits ([
Chbb:CH); n = 40),
Interventions: Endotoxin was given to 30 animals. Ten animals received no i
nhibitor (endotoxin control group). The other animals were either treated b
y high-dose (300 units/kg; n = 10) or low-dose (100 units/kg; n = 10)combin
ed antithrombin III and C1-esterase inhibitor administration, Ten rabbits (
time control group) were given placebo (sodium chloride 0.9%), Cardiorespir
atory variables were assessed at baseline, 120 mins, and 240 mins after end
otoxin or placebo administration. Four hours after endotoxin injection, liv
er, lung, and kidney tissue samples were examined for intravascular fibrin
deposition by light microscopy.
Measurements and Main Results: Inhibitor treatment significantly decreased
clot formation in lungs and livers without, however, demonstrating a clear
dose dependent effect. Combined antithrombin III/C1-esterase treatment atte
nuated the decrease of mean arterial pressure and cardiac output observed f
ollowing endotoxin injection. Blood pressure improvement was significantly
dependent on dosage administered.
Conclusion: Combination of antithrombin III and C1-esterase inhibitor treat
ment during early endotoxin shock decreased organ fibrin deposition and imp
roved cardiovascular stability.