Xu Ru Kun, Ding Pei Cheng, Wang JianKai, Liu YiMing, Wang Lei, Shi HongWei, Wang XiaoLiang
Department of Anesthesiology, Nanjing First Hospital, Nanjing Medical University, Jiangsu, China.
Department of Cardiothoracic Surgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Perfusion. 2023 Aug 26:2676591231199214. doi: 10.1177/02676591231199214.
A small animal model would be an effective tool for research on the pathophysiology of cardiopulmonary bypass (CPB). However, numerous CPB models do not involve myocardial arrest and resuscitation. The aim of this research is to establish an easily achievable myocardial arrest and resuscitation CPB model through hyperkalemia and landiolol, simulating clinical cardiac surgery.
Ten Sprague-Dawley rats were chosen for CPB. Rats underwent sevoflurane inhalation induction anesthesia and were sustained in an anesthesia state by intubation and intraperitoneal injection's of esketamine and propofol. The entire CPB circuit include a reservoir, a membrane oxygenator and a roller pump, which were connected into a complete loop via silicon tubes and infusion tube.After CPB was established through the tail artery and internal jugular vein, cardioplegic arrest was induced and maintained for 5 min at a rectum temperature of 28.5 ± 0.5°C with hyperkalemia and landiolol. Calcium chloride, epinephrine and insulin were then used for resuscitation.
All rats successfully finished cardioplegic arrest, resuscitation procedure and survived 2 h postoperatively. Mean hematocrit during CPB was significantly lower than physiologic values of the baseline. The mean time of arrest-resuscitation and CPB was 5.4 ± 0.8 min and 98.5 ± 5.0 min. The blood gas at each detection point were in range with the normal standard requirement of CPB.
The establishment of cardioplegic arrest and resuscitation procedure via hyperkalemia and landiolol during CPB of WD rat could be achieved successfully. This animal model could be an alternative organ injury research on organ injury of patients undergoing cardiac surgery.
小动物模型将是研究体外循环(CPB)病理生理学的有效工具。然而,众多CPB模型未涉及心肌停搏和复苏。本研究的目的是通过高钾血症和兰地洛尔建立一种易于实现的心肌停搏和复苏CPB模型,以模拟临床心脏手术。
选择10只Sprague-Dawley大鼠进行CPB。大鼠经七氟醚吸入诱导麻醉,并通过插管及腹腔注射艾司氯胺酮和丙泊酚维持麻醉状态。整个CPB回路包括一个储液器、一个膜式氧合器和一个滚压泵,它们通过硅胶管和输液管连接成一个完整的环路。经尾动脉和颈内静脉建立CPB后,在直肠温度为28.5±0.5°C时,用高钾血症和兰地洛尔诱导并维持心脏停搏5分钟。然后使用氯化钙、肾上腺素和胰岛素进行复苏。
所有大鼠均成功完成心脏停搏、复苏过程,并在术后存活2小时。CPB期间的平均血细胞比容显著低于基线生理值。心脏停搏-复苏和CPB的平均时间分别为5.4±0.8分钟和98.5±5.0分钟。各检测点的血气均符合CPB的正常标准要求。
在Wistar大鼠CPB期间,通过高钾血症和兰地洛尔成功建立心脏停搏和复苏程序是可行的。该动物模型可作为研究心脏手术患者器官损伤的替代模型。