Li G C, Vasquez J A, Gallagher K P, Lucchesi B R
Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109-0626.
Circulation. 1990 Aug;82(2):609-19. doi: 10.1161/01.cir.82.2.609.
Myocardial preconditioning with brief coronary artery occlusions before a sustained ischemic period is reported to reduce infarct size. To determine the number of occlusive episodes required to produce the preconditioning effect, we performed single or multiple occlusions of the left circumflex coronary artery (LCx) followed by a sustained occlusion (60 minutes) of the LCx. Anesthetized dogs underwent one (P1), six (P6), or 12 (P12) 5-minute occlusions of the LCx. Each occlusion period was followed by a 10-minute reperfusion period. A 60-minute occlusion of the LCx followed the preconditioning sequences. A control group received a 60-minute occlusion of the LCx without preconditioning. All groups were subjected to 6 hours of reperfusion after which the heart was removed for calculating infarct size (IS), area at risk (AR), and left ventricular mass (LV). The IS/AR ratio for the control group was 29.8 +/- 4.4% (n = 17), which was substantially greater (p less than 0.001) than that of the preconditioned groups: P1, 3.9 +/- 1.3% (n = 14); P6, 0.4 +/- 0.3% (n = 5); and P12, 2.9 +/- 2.8% (n = 5). There were no significant differences in the IS/AR ratio among the three preconditioned groups. The AR/LV ratio was comparable among all groups and did not differ statistically: control, 40.4 +/- 1.3%; P1, 36.2 +/- 1.7%; P6, 36.1 +/- 1.7%; and P12, 37.3 +/- 2.1%. Collateral blood flow to the inner two thirds of the risk region determined with radiolabeled microspheres during ischemia did not differ significantly between the control group (0.03 +/- 0.01 ml/min/g, n = 8) and single occlusion group (0.06 +/- 0.02 ml/min/g, n = 8), indicating that the marked disparity in infarct size could not be attributed to differences in collateral blood flow. The data indicate that preconditioning with one brief ischemic interval is as effective as preconditioning with multiple ischemic periods.
据报道,在持续缺血期之前短暂阻断冠状动脉进行心肌预处理可减小梗死面积。为了确定产生预处理效果所需的阻断次数,我们对左旋冠状动脉(LCx)进行单次或多次阻断,随后对LCx进行持续阻断(60分钟)。麻醉的犬接受1次(P1)、6次(P6)或12次(P12)5分钟的LCx阻断。每次阻断期后接着是10分钟的再灌注期。在预处理序列后对LCx进行60分钟的阻断。对照组接受一次60分钟的LCx阻断,不进行预处理。所有组均接受6小时的再灌注,之后取出心脏计算梗死面积(IS)、危险区域面积(AR)和左心室质量(LV)。对照组的IS/AR比值为29.8±4.4%(n = 17),显著高于(p<0.001)预处理组:P1组为3.9±1.3%(n = 14);P6组为0.4±0.3%(n = 5);P12组为2.9±2.8%(n = 5)。三个预处理组之间的IS/AR比值无显著差异。所有组的AR/LV比值相当,无统计学差异:对照组为40.4±1.3%;P1组为36.2±1.7%;P6组为36.1±1.7%;P12组为37.3±2.1%。在缺血期间用放射性微球测定的危险区域内三分之二的侧支血流量在对照组(0.03±0.01 ml/min/g,n = 8)和单次阻断组(0.06±0.02 ml/min/g,n = 8)之间无显著差异,表明梗死面积的显著差异不能归因于侧支血流量的差异。数据表明,一次短暂缺血间隔的预处理与多次缺血期的预处理效果相同。