TY - JOUR
T1 - Peroxynitrite Decreases Rabbit Tissue Factor Activity In Vitro
AU - Nielsen, Vance G.
AU - Crow, John P.
PY - 2004/3
Y1 - 2004/3
N2 - Tissue factor (TF) is a primary initiator of physiological coagulation in vivo. Peroxynitrite (OONO-), a molecule formed from nitric oxide (NO) and superoxide (O2 · -), decreases human TF activity in vitro. Coagulopathy has been associated with hepatoenteric ischemia-reperfusion known to involve formation of OONO-. Further, circulating TF activity decreases in rabbits after hepatoenteric ischemia-reperfusion. We hypothesized that exposure of rabbit TF to OONO - would result in a decrease in activity. OONO- generation was performed with 3-morpholinosydnonimine (SIN-1), a molecule that produces both nitric oxide and superoxide. Rabbit brain TF was incubated at 37°C for 90 min with 1) 0 mM SIN-1, 2) 5 mM SIN-1, 3) 5 mM SIN-1 and 2000 U/mL recombinant human superoxide dismutase (hSOD1), or 4) 2000 U/mL hSOD1 (n = 8 per condition). TF activity was assessed by addition of TF samples to human plasma and measuring clot formation kinetics with a thrombelastograph®. TF exposure to SIN-1 resulted in a 48% decrease in activity that was significantly different from the other three conditions (P < 0.001). There were no significant differences between the other conditions. We conclude that rabbit TF is inhibited by OONO-, and further investigation to determine the role of OONO- in coagulopathies associated with hepatoenteric ischemia-reperfusion is warranted.
AB - Tissue factor (TF) is a primary initiator of physiological coagulation in vivo. Peroxynitrite (OONO-), a molecule formed from nitric oxide (NO) and superoxide (O2 · -), decreases human TF activity in vitro. Coagulopathy has been associated with hepatoenteric ischemia-reperfusion known to involve formation of OONO-. Further, circulating TF activity decreases in rabbits after hepatoenteric ischemia-reperfusion. We hypothesized that exposure of rabbit TF to OONO - would result in a decrease in activity. OONO- generation was performed with 3-morpholinosydnonimine (SIN-1), a molecule that produces both nitric oxide and superoxide. Rabbit brain TF was incubated at 37°C for 90 min with 1) 0 mM SIN-1, 2) 5 mM SIN-1, 3) 5 mM SIN-1 and 2000 U/mL recombinant human superoxide dismutase (hSOD1), or 4) 2000 U/mL hSOD1 (n = 8 per condition). TF activity was assessed by addition of TF samples to human plasma and measuring clot formation kinetics with a thrombelastograph®. TF exposure to SIN-1 resulted in a 48% decrease in activity that was significantly different from the other three conditions (P < 0.001). There were no significant differences between the other conditions. We conclude that rabbit TF is inhibited by OONO-, and further investigation to determine the role of OONO- in coagulopathies associated with hepatoenteric ischemia-reperfusion is warranted.
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U2 - 10.1213/01.ANE.0000101988.62847.0C
DO - 10.1213/01.ANE.0000101988.62847.0C
M3 - Article
C2 - 14980916
SN - 0003-2999
VL - 98
SP - 668
EP - 671
JO - Anesthesia and analgesia
JF - Anesthesia and analgesia
IS - 3
ER -