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A Rat Model of Pulmonary Infection After Cardiac Transplant

机译:心脏移植后肺部感染的大鼠模型

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Objectives: Cardiac allograft rejection and infection are leading causes of morbidity and mortality after transplant. The lack of an animal model has hindered related research. We have developed a rat model of pulmonary infection after cardiac transplant to address this issue. Materials and Methods: Lewis rats received Wistar rat heart allografts, cardiac rejection was induced by cessation of cyclosporine injection, and pulmonary infection was induced by Pseudomonas aeruginosa intrabronchial inoculation. Development of pul-monary infection and/or heart rejection was assessed by histopathology. Results: Histopathologic findings showed that a dose of 2 × 10 8 colony forming units of Pseudo-monas aeruginosa intrabronchial inoculation is sufficient to cause severe pneumonia without being lethal to transplanted animals. Daily administration of 10 mg/kg of cyclosporine reliably suppressed rejection, and withdrawal for 7 days can obtain a consistent International Society for Heart and Lung Transplantation 3R rejection. Conclusions: The current study represents a simple and effective rat model of pulmonary infection along, or in combination, with rejection after heart transplant, which can be used for research of infection-rejection in cardiac transplant settings.
机译:目的:心脏同种异体移植排斥和感染是移植后发病和死亡的主要原因。动物模型的缺乏阻碍了相关研究。我们已经开发了心脏移植后肺部感染的大鼠模型来解决这个问题。材料与方法:Lewis大鼠接受Wistar大鼠心脏同种异体移植,停止环孢菌素注射引起心脏排斥反应,铜绿假单胞菌支气管内接种诱导肺部感染。通过组织病理学评估了肺部感染和/或心脏排斥反应的发生。结果:组织病理学结果显示,铜绿假单胞菌支气管内接种剂量为2×10 8个菌落形成单位,足以引起严重的肺炎,而不会对移植的动物致死。每天施用10 mg / kg的环孢菌素能可靠地抑制排斥反应,而停药7天可以得到国际心肺移植3R排斥反应的一致性。结论:本研究代表了一种简单有效的大鼠肺部感染模型,该模型与心脏移植后排斥反应并存或与之结合,可用于研究心脏移植环境中的感染抑制。

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