期刊文献+

大鼠体外循环肺损伤动物模型的建立

Establishment of a Rat Model of CPB
下载PDF
导出
摘要 目的为研究大鼠体外循环(CPB)中肺损伤机制与肺保护方法,建立大鼠体外循环肺损伤动物模型。方法雄性SD大鼠30只分为两组,麻醉开胸组10只,体外循环组20只(实验鼠和供血鼠各加10只),颈静脉和股动脉插管,建立体外循环,流量120~150 mL/min,预充液10 mL全血,5 mL代血浆,同时胸骨正中切口阻断肺动脉1 h后开放,逐渐脱离体外循环,开胸对照组10只是开胸全麻。结果所有数据均显示10例体外循环动物模型均建立成功。结论大鼠体外循环肺损伤动物模型方法上是可行的,是研究体外循环肺损伤的优良动物模型。 Objective To establish a rat model of CPB and to investigate the CPB-related lung dysfanction and possible protective interventions. Methods Male SD rats(240-260 g)were randomly divided into CPB(n=10)group and Sham group(n=10). All rats were anaesthetized and mechanically ventilated. The femoral artery and vein were cannulated for continuous blood pressure recordings and fluid replacement, respectively. The CPB circuit comprised a venous reservoir,a membrane oxygenator,and a roller pump. Blood was drained from the right atrium via a jugular vein catheter and returned to the right carotid artery. Priming consisted of 10 mL of homologous blood and 5 mL of colloid. CPB was conducted for 90 rain at a flow rate of 1204 150 mL/kg/min in the CPB group. Haemodynamic investigations, blood gas analysis, and survival studies were performed subsequently. Results Our data showed that the rat model principally simulated the clinical setting of CPB in terms of its construction, configuration, performance, material surface area, and priming volume to blood volume ratio. All CPB rats survived and haemodynamic investigations,blood gas analysis were normal. Conclusion The rat model of CPB was easy to establish and should facilitate the investigation of the pathophysiological processes concerning CPB-related lung dysfunction and possible protective interventions.
出处 《江西医学院学报》 CAS 2007年第4期1-4,共4页 Acta Academiae Medicinae Jiangxi
基金 国家高技术研究发展计划(863计划)(2001AA216061)
关键词 体外循环 大鼠 肺损伤 extracorporeal circulation Rats lung injury
  • 相关文献

参考文献17

  • 1Palanzo D A.Perfusion Safety:Past,Present,and Future[J].J Cardiothorac Vasc Anesth,1997,11:383. 被引量:1
  • 2Paparella D,Yau T M,Young E.Cardiopulmonary Bypass Induced Inflammation:Pathophysiology and Treatment.An update Eur[J].J Cardiothorac Surg,2004,21:232. 被引量:1
  • 3Levy J H,Tanaka K A.Inflammatory Response to Cardiopulmonary Bypass[J].Ann Thorac Surg,2003,75:S715. 被引量:1
  • 4Hiramatsu Y,Gikakis N,Gorman J H.A Baboon Model for Hematologic Studies of Cardiopulmonary Bypass[J].J Lab Clin Med,1997,130:412. 被引量:1
  • 5Kim W G,Moon H J,Won T H.Rabbit Model of Cardiopulmonary Bypass[J].Perfusion,1999,14:101. 被引量:1
  • 6Wittnich C,Belanger M P,Wallen W J.A Long-term Stable Normothermic Cardiopulmonary Bypass Model in Neonatal Swine[J].J Surg Res,2001,101:176. 被引量:1
  • 7Dong X,Liu Y,Du M,et al.P38 Mitogen-activated Protein Kinase Inhibition Attenuates Pulmonary Inflammatory Response in a Rat Cardiopulmonary Bypass Model[J].Eur J Cardiothorac Surg,2006,30(1):77-84. 被引量:1
  • 8Xiao da W,Yang M,Yang J,et al.Lung Damage May Induce Thrombocytopenia[J].Platelets,2006,17(5):347-349. 被引量:1
  • 9An Y,Xiao Y,Zhong Q.Good Recovery after Nontransthoracic Cardiopulmonary Bypass in Rats[J].Heart Surg Forum,2007,10(1):E73-77. 被引量:1
  • 10Yoshitani K,de Lange F,Ma Q,et al.Reduction in Air Bubble Size Using Perfluorocarbons During Cardiopulmonary Bypass in the Rat[J].Anesth Analg,2006,103(5):1089-1093. 被引量:1

二级参考文献4

  • 1张根成 易定华 汪曾炜 等.兔体外循环动物模型的建立[J].中国循环杂志,1998,13:313-313. 被引量:3
  • 2[1]Yoshitaka H,Yoshiki S, Motonobu N, et al. P - selectin monoclonal antibody may attenuate the whole body inflammatory response induced by cardiopulmonary bypass [J]. ASAIO Journal,2000,46: 334 -337. 被引量:1
  • 3[2]Liu Y,Wang Q,Zhu X, et al. Pulmonary artery perfusion with protective solution reduces lung injury after cardiopulmonary bypass[J]. Ann Thorac Surg,2000 ,65 :1402 -1407. 被引量:1
  • 4[4]Adrian J,Levine FRCS,Karen P, et al. The effect of adhesion molecule blockade on pulmonary reperfusion injury [J]. Ann Thorac Surg,2002,73: 1101 - 1106. 被引量:1

共引文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部