Tf. Tvedskov et al., STUDIES OF THE INITIAL ANTICOAGULANT RESPONSE IN TISSUE-THROMBOPLASTIN INDUCED INTRAVASCULAR COAGULATION, Blood coagulation & fibrinolysis, 7(6), 1996, pp. 595-601
The very early anticoagulant response was analysed in non-pregnant fem
ale New Zealand rabbits infused with rabbit brain tissue thromboplasti
n for a period of 10 min (n = 6), 20 min (n = 6), and 30 min (n = 6).
The rabbits infused with thromboplastin responded with a significant d
rop in mean arterial pressure (P < 0.05), an increase in blood p(a)O(2
) (P < 0.05) and a decrease in p(a)CO(2) (P < 0.05), while control ani
mals remained stable with respect to these variables. The thromboplast
in-treated animals had an immediate drop in platelet count (P < 0.05),
plasma fibrinogen (P < 0.05) and a prolongation in prothrombin time (
P < 0.05) and activated partial thromboplastin time (P < 0.05). The co
ncentrations in a number of proteins involved in the anticoagulant res
ponse (antithrombin, plasminogen, antiplasmin) as well as global fibri
nolytic activity did not change significantly following 10, 20 and 30
min infusion of thromboplastin, while the concentration of protein C d
ecreased continuously during the infusion periods (P < 0.05) to reach
the lowest level (similar to 60%) in animals infused with thromboplast
in for 30 min. The animals infused with tissue thromboplastin had micr
othrombi in 1-6% of the renal glomeruli, but the number of microthromb
i did not differ significantly between animals infused for 10, 20 and
30 min. It is concluded that the protein C system may play a key role
during the initial phase of intravascular coagulation and immediate ac
tivation of protein C may protect against excessive deposition of fibr
in.