Zhang Yinbing, Liu Haifeng, Zhang Yingqian, Wu Qiong, Zhang Yanyan, Zhang Jie, Zhou Xiangshan, Jiao He, Fan Feng, Xue Qi, Wang Xin, Zhong Zhihui
Laboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China,
Sichuan Kangcheng Biomed Co., Ltd., Chengdu, China,
Drug Des Devel Ther. 2018 Nov 1;12:3717-3730. doi: 10.2147/DDDT.S180151. eCollection 2018.
In order to evaluate the thrombolytic effects of reteplase in pulmonary thromboembolism (PTE), we developed a novel canine PTE model. The efficacy of reteplase against PTE in comparison to alteplase was clarified for the first time, and this PTE model could be further applied to studies of novel thrombolytic therapies.
Twenty-four dogs were divided into four groups: sham operation, vehicle, alteplase, and reteplase. Autologous thrombi/saline were injected into the pulmonary artery, and thrombolytic agents were administrated. Thrombus formation and dissolution were monitored by real-time digital subtraction angiography (DSA), and pulmonary pressures were measured simultaneously. Blood coagulation, blood gas, hematology, and histopathologic examinations were used as subsidiary methods.
The canine PTE model was established with a significant decrease of blood flow and ~75% blocking area. Administration of reteplase (0.6 mg/kg) resulted in effective thrombus dissolution with a recovery of over 80% blood flow, as effective as alteplase (1.6 mg/kg). Correspondingly, the elevated pulmonary systolic, diastolic, and mean arterial pressures declined to the normal level. Blood coagulation was changed by reteplase, with a dramatic elongation of prothrombin time, activated partial thromboplastin time, and thrombin time, even longer than alteplase. In contrast to the vehicle group, no obvious pathological changes were found in the two thrombolytic groups. Hematological, blood biochemical, and blood gas results also indicated that reteplase had no adverse reactions in this PTE model.
Reteplase proved to be an effective and safe therapy for PTE for the first time, and a small dosage of reteplase exerted an efficacy comparable to the routine dosage of alteplase. Our findings indicated the potential of reteplase as clinical treatment against PTE. This technically innovative, stability- and validity-proved canine PTE model developed by minimally invasive surgery and DSA resembled major clinical features. This may further facilitate our understanding of thrombotic disorders and development of prophylactic and therapeutic approaches.
为了评估瑞替普酶对肺血栓栓塞症(PTE)的溶栓效果,我们建立了一种新型犬PTE模型。首次明确了瑞替普酶与阿替普酶相比对PTE的疗效,并且该PTE模型可进一步应用于新型溶栓疗法的研究。
将24只犬分为四组:假手术组、溶剂对照组、阿替普酶组和瑞替普酶组。将自体血栓/生理盐水注入肺动脉,并给予溶栓药物。通过实时数字减影血管造影(DSA)监测血栓形成和溶解情况,并同时测量肺动脉压力。采用凝血、血气、血液学和组织病理学检查作为辅助方法。
建立的犬PTE模型血流显著减少,阻塞面积约为75%。给予瑞替普酶(0.6mg/kg)可有效溶解血栓,血流恢复超过80%,与阿替普酶(1.6mg/kg)效果相当。相应地,升高的肺动脉收缩压、舒张压和平均动脉压降至正常水平。瑞替普酶改变了凝血情况,凝血酶原时间、活化部分凝血活酶时间和凝血酶时间显著延长,甚至比阿替普酶组更长。与溶剂对照组相比,两个溶栓组未发现明显病理变化。血液学、血液生化和血气结果也表明,瑞替普酶在该PTE模型中无不良反应。
首次证明瑞替普酶是一种治疗PTE安全有效的疗法,小剂量瑞替普酶的疗效与阿替普酶常规剂量相当。我们的研究结果表明瑞替普酶具有作为PTE临床治疗药物的潜力。通过微创手术和DSA建立的这种技术创新、稳定性和有效性得到验证的犬PTE模型与主要临床特征相似。这可能进一步促进我们对血栓性疾病的理解以及预防和治疗方法的开发。