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Establishment of a novel rat model without blood priming during normothermic cardiopulmonary bypass

机译:常温体外循环过程中无血液灌注的新型大鼠模型的建立

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Objective: An effective animal model was needed for research on the pathophysiology of cardiopulmonary bypass (CPB). Rat models were considered suitable for research into CPB, recently. The aim of the article is to establish a simple and safe CPB model without blood priming in rats, containing the advantages of controlling temperature precisely, being similar to the clinical process and laying the foundation for the further study of a deep hypothermic circulatory arrest (DHCA) model. Materials and Methods: Ten Sprague-Dawley rats, divided into a CPB group (n=7) and a sham group (n=3), received sevoflurane inhalation anesthesia and were maintained in an anesthesia state by intubation. The entire CPB circuit consisted of a reservoir, a membrane oxygenator, a roller pump, a heat exchanger and a heat cooler, all of which were connected via silicon tubes. The volume of the priming solution, composed of 6% HES130/0.4 and 125 IU heparin, was less than 12 ml. In the CPB group, a 22G catheter was placed in the left femoral artery for monitoring arterial blood pressure, a 20G catheter was placed in a tail artery for arterial inflow and a homemade, multiorificed catheter was inserted into a right jugular vein for venous drainage. After 90 minutes, the CPB process was terminated when vital signs were stable. In the sham group, the same surgical process was conducted except for the venous drainage. Post-oxygenator blood gas and hemodynamic parameters were measured at each time point before CPB, during CPB and after CPB. Results: All CPB processes were successfully achieved. Blood gas analysis and hemodynamic parameters of each time point were in accordance with normal ranges. The vital signs of all rats were stable. Conclusion: The establishment of CPB without blood priming in rats can be achieved successfully. The rat model could be used to study short-term or long-term organ injury mechanisms caused by CPB. Furthermore, on the basis of the precise control of temperature and the depth of anesthesia, the DHCA model in rats could be developed further to study pathophysiological changes of neurological and other organ functions in the future.
机译:目的:需要一种有效的动物模型来研究体外循环(CPB)的病理生理。最近,大鼠模型被认为适合研究CPB。本文的目的是建立一种简单,安全的无血流刺激的大鼠CPB模型,该模型具有精确控制温度的优点,与临床过程相似,为进一步研究深低温循环性停搏(DHCA)奠定了基础)模型。材料与方法:将十只Sprague-Dawley大鼠分为CPB组(n = 7)和假组(n = 3),接受七氟醚吸入麻醉,并通过插管维持麻醉状态。整个CPB回路由一个储罐,一个膜式充氧器,一个辊泵,一个热交换器和一个冷却器组成,所有这些都通过硅管连接。由6%HES130 / 0.4和125 IU肝素组成的灌注溶液的体积小于12 ml。在CPB组中,将22G导管置于左股动脉中以监测动脉血压,将20G导管置于尾动脉中以供动脉流入,并将自制的多孔导管插入右颈静脉以进行静脉引流。 90分钟后,生命体征稳定后,CPB流程终止。在假手术组中,除了静脉引流外,进行了相同的手术过程。在CPB之前,CPB期间和CPB之后的每个时间点,测量氧合器后的血气和血液动力学参数。结果:所有CPB流程均成功实现。每个时间点的血气分析和血液动力学参数均在正常范围内。所有大鼠的生命体征稳定。结论:可成功建立无血源性CPB。大鼠模型可用于研究由CPB引起的短期或长期器官损伤机制。此外,在精确控制温度和麻醉深度的基础上,将来可进一步建立大鼠DHCA模型,以研究神经和其他器官功能的病理生理变化。

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