Efficacy evaluation of r-SaK in a novel canine acute cerebral vessel thromboembolism model

Author:

HONG Qian1,LI Ming2,ZHANG Peng2,WANG Yu2,Zhou Jianming3,XIAO Lu1,WANG Ying1,LIAN Li1,YAN Zhao2

Affiliation:

1. The Affiliated Huaihai Hospital of Xuzhou Medical University (the 71st Group Army Hospital of CPLA Army)

2. Xuzhou New Health Hospital

3. Jiangsu Kanion Modern TCM Research Institute

Abstract

Abstract In order to evaluate the thrombolytic effect of Recombinant staphylokinase for injection (r-SaK) in acute ischemic cerebral infarction, an intracranial large vessel occlusion animal model was generated by pushing an autologous thrombus to the internal carotid artery under X-ray angiography. Thirty dogs were divided into five groups: model group, alteplase group, and r-SaK group (three dosages). Autologous thrombi/saline were injected into the internal carotid artery, and thrombolytic agents were then administrated. Thrombus formation and dissolution were monitored by real-time digital subtraction angiography (DSA), blood coagulation and histopathologic examinations were used as subsidiary methods. The results in the present study showed that the left cerebral vascular thrombotic occlusion model was established stably after the autologous thrombus pushed through the internal carotid artery in dogs. Administration of r-SaK (0.25, 0.5, 1.0 mg/kg) produced effective thrombus dissolution with a recovery of over 80% blood flow, as effective as alteplase (1.68 mg/kg). Correspondingly, blood coagulation was changed by r-SaK, with a dramatic elongation of prothrombin time (PT), activated partial thromboplastin time (APTT), and thrombin time (TT) and reduction of fibrinogen (FIB). In contrast to the model group, pathological improvement in the two thrombolytic groups were mainly manifested in the improvement of the structural integrity of the gray matter, and the reduction of the infiltration of inflammatory cells and neuronal damage in the intracranial blood vessels. Besides, no adverse reactions related to bleeding in this model were found. The results indicate that intravenous infusion of r-SaK has a significant thrombolytic effect on intracranial large vessel occlusion model, and can prevents brain tissue and neuron damage induced by thromboembolism. We also provide a new preclinical pharmacodynamic evaluation method (DTICI) of cerebral thrombolytics using beagle dogs with an acute thrombotic cerebrovascular occlusion, The efficacy of r-SaK against acute thrombotic cerebral vessel occlusion in comparison to alteplase was also clarified for the first time, and this model could be further applied to studies of novel thrombolytic therapies.

Publisher

Research Square Platform LLC

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