Induction of DIC by Russell’s Viper Venom in the Rat. Preventive Activity of Ticlopidine on Consumption Coagulopathy
The intraperitoneal administration of the LD50 dose of Russell’s viper venom to Sprague Dawley rats induces a DIC with consumption coagulopathy. The PT, TT and APTT are increased and the recalcification time and platelet count is considerably decreased. Also the thromboelastogram is quite perturbed. In order to follow the modifications of the coagulation parameters induced by the venom in the presence and absence of Ticlopidine. Four groups of each eight animals are investigated : Control, Ticlopidine 150 mg/kg/d. P.O. 4 days, Venom LD5O of Russell’s venom viper (Sigma), i.e. 400 μg/kg by I.P. route, 15 hrs before sacrifice, Ticlopidine + Venom T. 150 mg/kq/d. P.O. 4 days and the LD50 venom 15 hrs before sacrifice. The venom showed versus control a significant increase of PT, and APTT a significant decrease of Recalcification time and platelet count. The prevention of the DIC by Ticlopidine is characterized by the normalization of the coagulation factors. In comparison with the venom the Ticlopidine group has an increase of rocalci-fication time and PT, TT, APTT and platelet count were identical with the control group. The fibrinogen level increase significantly. The histopathological examination of kidneys and lunqs show the characteristic lesions of DIC in the venom animals, and the protective activity of Ticlopidine versus the intravascular aggregats in the Ticlopidine venom group. No protection by Ticlopidine however, was shown against the neurotoxicity of the venom. The inhibition of platelet aggregats and the antithrombotic activity of a drug can be evaluated by this experimental model of an acute DIC.