Alexandre Joachim, Schiariti Michele, Rouet René, Puddu Paolo Emilio
CHU de Caen, Department of Cardiology F-14000 Caen, France;
Int J Physiol Pathophysiol Pharmacol. 2013;5(1):52-60. Epub 2013 Mar 8.
An ischemia/reperfusion-simulating model in rabbit tissue should be right oriented and clinically relevant to provide a non expensive approach for manipulations of currents involved in the repolarization process. Standard right ventricular guinea-pig (N=18) and newly investigated rabbit (N=12) myocardial strips were placed in a special perfusion chamber allowing partition into two segments independently superfused with oxygenated Tyrode's solution or a modified Tyrode's solution mimicking ischemia by: 1) increased extracellular potassium concentration (12 mmol/L), 2) decreased HCO3 (-) concentration (9 mmol/L), leading to a decrease in pH (6.90 ± 0.05), 3) decreased pO2 by replacement of 95% O2 and 5% CO2 by 95% N2 and 5% CO2 gas mixture, and 4) complete withdrawal of glucose. There were significant differences in rabbit as compared to guinea-pig preparations in baseline (p<0.02) and post-ischemic-like (p<0.01) APA and RMP with lower values in the formers, and lower post-ischemic Vmax in rabbit preparations (25±15 versus 97±83 V/s, p<0.01) but neither baseline nor post-ischemic-like or absolute changes in APD50, APD90 were different. In ischemia- and reperfusion-like phases, there were high proportions of single spontaneous repetitive responses, both in guinea-pig (respectively 50 and 89%) and rabbit preparations (respectively 67 and 92%). Guinea-pig preparations showed higher incidence of severe spontaneous repetitive responses (61 versus 17%, p<0.02). This rabbit model is proposed to investigate both anti- and pro-arrhythmic effects of drugs acting at various levels electrophysiologically, which may be obtained with great power and relatively few (around 10 per group) preparations. This model should now be tested pharmacologically.
兔组织中的缺血/再灌注模拟模型应定位正确且具有临床相关性,以便为操纵复极化过程中涉及的电流提供一种经济的方法。将标准的豚鼠右心室(N = 18)和新研究的兔(N = 12)心肌条置于一个特殊的灌注室中,该灌注室可分为两个部分,分别用含氧的台氏液或通过以下方式模拟缺血的改良台氏液进行独立灌注:1)增加细胞外钾浓度(12 mmol/L),2)降低HCO3(-)浓度(9 mmol/L),导致pH值降低(6.90±0.05),3)用95% N2和5% CO2的气体混合物替代95% O2和5% CO2,降低pO2,4)完全去除葡萄糖。与豚鼠制剂相比,兔制剂在基线(p<0.02)和缺血样后(p<0.01)的动作电位幅度(APA)和静息膜电位(RMP)存在显著差异,前者的值较低,兔制剂缺血后的最大上升速率(Vmax)较低(25±15对97±83 V/s,p<0.01),但动作电位时程50%(APD50)、动作电位时程90%(APD90)的基线、缺血样后或绝对变化均无差异。在缺血和再灌注样阶段,豚鼠(分别为50%和89%)和兔制剂(分别为67%和92%)中都有高比例的单个自发重复反应。豚鼠制剂中严重自发重复反应的发生率更高(61%对17%,p<0.02)。该兔模型被提议用于研究在电生理各个水平起作用的药物的抗心律失常和促心律失常作用,使用相对较少(每组约10个)的制剂就能获得强大的效果。现在应该对该模型进行药理学测试。