Fukuyama T, Sobel B E, Roberts R
Cardiovasc Res. 1984 May;18(5):310-20. doi: 10.1093/cvr/18.5.310.
Beneficial effects of reperfusion or revascularisation on acute myocardial injury may be restricted to the initial few hours due in part to the development of myocardial haemorrhage and "no-reflow". In the present study, the severity of regional myocardial haemorrhage was assessed with Cr-51-RBC and compared with regional flow in the same areas assessed with labelled microspheres in 51 dogs to determine the temporal profile of reperfusion induced haemorrhage and "no-reflow" in relation to the duration of preceding ischaemia. Reperfusion was initiated after selected intervals of coronary occlusion (1 to 7 h) in 31 dogs, and results compared to those in 14 dogs with persistent occlusion and six dogs with no occlusion. Regions of decreased perfusion were outlined grossly with lissamine dye. Heart rate, blood pressure and left atrial pressures were monitored continuously. Haemorrhage was confirmed by histology. The amount of blood in normal regions of the heart was 3.2 +/- 0.4% of wet weight. In tissue ischaemic for 1 h without reperfusion, it was less, ie, 2.3 +/- 0.7; with occlusion of seven hours, it was reduced even further to 1.3%. in dogs subjected to reperfusion after selected intervals of ischaemia, haemorrhage (6.6 +/- 3.8 ml X 100 g-1) occurred in the endocardium after 3 h of ischaemia but in this epicardium only after 5 h of ischaemia (3.9 +/- 1). Regional flow was normal in the endocardium with reperfusion after 1 h of ischaemia (0.9 +/- 0.2 ml X min-1 X g-1) but decreased by 50% with ischaemia of 7 h prior to reperfusion. Thus, haemorrhage occurred earlier than "no-reflow". Results indicate that the severity of microvascular damage is a function of the duration of the interval of ischaemia prior to reperfusion and that it is evident earliest in the subendocardium. Since haemorrhage preceded "no-reflow" extravasation of blood may contribute to the "no-reflow" phenomenon. Adjunctive measures designed to delay microvascular deterioration may be useful to prolong the interval in which lysis or bypass surgery can be implemented effectively.
再灌注或血管重建对急性心肌损伤的有益作用可能仅限于最初的几个小时,部分原因是心肌出血和“无复流”现象的出现。在本研究中,用铬-51标记的红细胞评估了51只犬局部心肌出血的严重程度,并与用标记微球评估的同一区域的局部血流进行比较,以确定再灌注诱导的出血和“无复流”与先前缺血持续时间的时间关系。31只犬在选定的冠状动脉闭塞间隔时间(1至7小时)后开始再灌注,并将结果与14只持续闭塞的犬和6只未闭塞的犬的结果进行比较。灌注减少的区域用丽丝胺染料大体勾勒出来。持续监测心率、血压和左心房压力。通过组织学证实出血情况。心脏正常区域的血量为湿重的3.2±0.4%。在缺血1小时未进行再灌注的组织中,血量较少,即2.3±0.7;缺血7小时时,血量进一步减少至1.3%。在缺血选定间隔时间后进行再灌注的犬中,缺血3小时后心内膜出现出血(6.6±3.8 ml×100 g-1),但缺血5小时后仅在心肌外层出现出血(3.9±1)。缺血1小时后再灌注时,心内膜局部血流正常(0.9±0.2 ml×min-1×g-1),但在再灌注前缺血7小时时血流减少50%。因此,出血比“无复流”出现得更早。结果表明,微血管损伤的严重程度是再灌注前缺血间隔时间的函数,并且最早在心肌内膜下明显。由于出血先于“无复流”出现,血液外渗可能导致“无复流”现象。旨在延缓微血管恶化的辅助措施可能有助于延长有效实施溶栓或搭桥手术的时间间隔。