H. Miyoshi, Y. Takayama, S. Kitashiro, T. Izuoka, D. Saito, Y. Imuro, J. Mimura, Satoshi Yamamoto, Mari Tokioka, T. Iwasaka
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引用次数: 4
摘要
临床研究证实缺血心肌邻近区域存在非缺血性区域功能障碍。最近的研究表明,血管紧张素II型1 (AT1)受体拮抗剂可减少心肌缺血再灌注损伤。我们通过研究at1受体拮抗剂对心肌功能和梗死面积的影响,探讨再灌注后邻近区域的作用。我们研究了12只开胸麻醉的狗,进行了90分钟的左冠状动脉前降支闭塞和4小时的再灌注。6只再灌注后立即注射at1受体拮抗剂(CV11974)的狗与6只对照狗进行比较。收缩期缩短百分比(%SS)是通过将两组对超声显微镜晶体植入邻近和远端非缺血心肌来测量的。再灌注4 h后,测量梗死面积。两个地区的基线SS %无显著差异。两组再灌注后邻近区%SS较远端区明显降低。两组间无显著差异。at组梗死面积占危险面积的百分比小于对照组(25.49+/-7.53% vs 68.58+/-26.88% P<0.01)。at1受体拮抗剂可减小梗死面积。这种影响与再灌注后邻近区域心肌功能的改变无关。
Influence of angiotensin II type 1-receptor antagonist CV11974 on infarct size and adjacent regional function after ischemia-reperfusion in dogs.
The presence of nonischemic regional dysfunction at the adjacent region of the ischemic myocardium was demonstrated in clinical studies. Recent studies demonstrated an angiotensin II type 1 (AT1)-receptor antagonist reduced myocardial ischemia-reperfusion injury. We investigated the role of the adjacent region after reperfusion by studying the effects of AT1-receptor antagonist on myocardial function and infarct size. We investigated 12 open-chest anesthetized dogs undergoing 90 min of left anterior descending coronary artery occlusion followed by 4 h of reperfusion. Six dogs injected with an AT1-receptor antagonist (CV11974) immediately after reperfusion were compared with 6 control dogs. Percent systolic shortening (%SS) was measured by two sets of the pair sonomicrometer crystals implanted to adjacent and remote nonischemic myocardium. After 4 h of reperfusion, infarct size was measured. There were no significant differences of the %SS at baseline between two regions. In both groups, %SS at adjacent region after reperfusion was significantly decreased as compared with remote region. There were no significant differences between the two groups. Infarct size, as a percentage of the area at risk, was smaller in the AT, group than in control group (25.49+/-7.53% vs 68.58+/-26.88% P<0.01). AT1-receptor antagonist reduces infarct size. This effect is not related to the change of regional myocardial function at adjacent region after reperfusion.