Ytrehus K, Gunnes S, Myklebust R, Mjøs O D
Institute of Medical Biology, University of Tromsø, Norway.
Cardiovasc Res. 1987 Jul;21(7):492-9. doi: 10.1093/cvr/21.7.492.
To determine the protective effect during ischaemia and reperfusion of removing oxygen radicals two groups of isolated Langendorff perfused rat hearts were arrested with cardioplegic solution at 4 degrees C and kept ischaemic at 15 degrees C for 210 min before being reperfused for 60 min at 37 degrees C. To remove oxygen radicals superoxide dismutase and catalase were added to the cardioplegic solution and to the buffer during the first 30 min of reperfusion in one group, the other group serving as control. At the end of reperfusion the first derivative of left ventricular developed pressure (dP/dt), coronary flow, high energy phosphate concentrations, and ultrastructure were determined. The ultrastructure was examined using a stereological method based on point counting and the results presented as volume fractions (Vv). DP/dt after 60 min of reperfusion was 61.6(5.6)% (mean (SEM)) of the initial values in the control group and 77.6(3.4)% in the superoxide dismutase and catalase supplemented group (p less than 0.05). In the supplemented group coronary flow was significantly higher than in the control group but only in the first part of reperfusion. The concentrations of adenosine triphosphate and creatine phosphate in the control group were 9.9(1.0) and 19.6(1.8) mumol.g-1 dry weight respectively; corresponding values in the supplemented group were 14.4(2.1) and 29.4(3.6) mumol.g-1 dry weight. The morphometric examination of the ultrastructure showed no significant difference in interstitial fluid accumulation evaluated by Vv(myocyte/myocardium) measurements and there was no difference in mitochondrial alteration between the two groups. There was, however, a significant reduction in the volume of cellular oedema (Vv(cell oedema/myocyte)) in the supplemented group.(ABSTRACT TRUNCATED AT 250 WORDS)
为了确定清除氧自由基在缺血及再灌注过程中的保护作用,将两组经Langendorff离体灌注的大鼠心脏用心脏停搏液在4℃停搏,于15℃保持缺血210分钟,然后在37℃再灌注60分钟。在再灌注的前30分钟,向一组心脏停搏液及缓冲液中加入超氧化物歧化酶和过氧化氢酶以清除氧自由基,另一组作为对照。再灌注结束时,测定左心室发展压的一阶导数(dP/dt)、冠脉流量、高能磷酸浓度及超微结构。超微结构采用基于点计数的体视学方法检查,结果以体积分数(Vv)表示。再灌注60分钟后,对照组dP/dt为初始值的61.6(5.6)%(均值(标准误)),超氧化物歧化酶和过氧化氢酶补充组为77.6(3.4)%(p<0.05)。补充组冠脉流量显著高于对照组,但仅在再灌注的第一阶段。对照组三磷酸腺苷和磷酸肌酸浓度分别为9.9(1.0)和19.6(1.8)μmol·g-1干重;补充组相应值分别为14.4(2.1)和29.4(3.6)μmol·g-1干重。超微结构的形态计量学检查显示,通过Vv(心肌细胞/心肌)测量评估的间质液积聚无显著差异,两组线粒体改变也无差异。然而,补充组细胞水肿体积(Vv(细胞水肿/心肌细胞))显著减少。(摘要截短于250词)