Myers M L, Bolli R, Lekich R F, Hartley C J, Roberts R
Circulation. 1985 Oct;72(4):915-21. doi: 10.1161/01.cir.72.4.915.
Reperfusion after reversible regional ischemia has been shown to result in delayed recovery of myocardial function, but the mechanism responsible for this phenomenon remains unknown. We explored the potential role of oxygen-free radicals as mediators of postischemic dysfunction in open-chest dogs undergoing a 15 min occlusion of the left anterior descending coronary artery (LAD) followed by 2 hr of reperfusion. Treated animals (n = 19) received an infusion of the oxygen free-radical scavengers superoxide dismutase (SOD; 15,000 U/kg) and catalase (CAT; 55,000 U/kg) for 1 hr starting 15 min before LAD occlusion, while control animals (n = 20) received an equal volume of saline. SOD and CAT produced no discernible effect on heart rate, aortic pressure, or left atrial pressure. Collateral flow to the ischemic zone (radioactive microspheres) was 0.07 +/- 0.01 ml/min/g in both groups. The size of the occluded bed as determined by postmortem perfusion was 26.1 +/- 1.2% of the left ventricle in the control group and 26.5 +/- 0.9% in the treated group. Systolic wall thickening (an index of regional function) was assessed with an epicardial pulsed-Doppler probe. The two groups exhibited comparable systolic thickening under baseline conditions and similar degrees of dyskinesia during ischemia. Nevertheless, recovery of function (expressed as percent of baseline) was considerably greater in the treated dogs, both at 1 hr (43.8 +/- 14.3 vs 12.8 +/- 11.6) and 2 hr of reperfusion (74.2 +/- 8.4 vs 31.6 +/- 9.8, p less than .005). This improved recovery of function obtained with SOD and CAT suggests that oxygen-free radicals play an important role in the genesis of myocardial dysfunction after a brief episode of regional ischemia.
可逆性局部缺血后的再灌注已被证明会导致心肌功能延迟恢复,但这种现象的机制仍不清楚。我们探讨了氧自由基在接受左冠状动脉前降支(LAD)15分钟闭塞及随后2小时再灌注的开胸犬缺血后功能障碍中的潜在介导作用。治疗组动物(n = 19)在LAD闭塞前15分钟开始接受1小时的氧自由基清除剂超氧化物歧化酶(SOD;15,000 U/kg)和过氧化氢酶(CAT;55,000 U/kg)输注,而对照组动物(n = 20)接受等体积的生理盐水。SOD和CAT对心率、主动脉压或左心房压无明显影响。两组缺血区的侧支血流(放射性微球)均为0.07±0.01 ml/min/g。通过死后灌注确定的闭塞心肌床大小在对照组为左心室的26.1±1.2%,治疗组为26.5±0.9%。用体表脉冲多普勒探头评估收缩期室壁增厚(局部功能指标)。两组在基线条件下收缩期增厚程度相当,缺血期间运动障碍程度相似。然而,治疗组犬在再灌注1小时(43.8±14.3对12.8±11.6)和2小时(74.2±8.4对31.6±9.8,p<0.005)时功能恢复(以基线百分比表示)明显更好。SOD和CAT获得的这种功能恢复改善表明,氧自由基在短暂局部缺血后心肌功能障碍的发生中起重要作用。