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通过氯化三苯基四氮唑染色与体内注射碘化丙啶测量梗死面积

Infarct size measurement by triphenyltetrazolium chloride staining versus in vivo injection of propidium iodide.

作者信息

Ito W D, Schaarschmidt S, Klask R, Hansen S, Schäfer H J, Mathey D, Bhakdi S

机构信息

Department of Cardiology, University Hospital Eppendorf, Hamburg, Germany.

出版信息

J Mol Cell Cardiol. 1997 Aug;29(8):2169-75. doi: 10.1006/jmcc.1997.0456.

Abstract

Infarct size delineation by triphenyltetrazolium chloride (TTC) staining is dependent on sufficient reperfusion. We therefore evaluated the possibility of using propidium iodide (PI), a reagent conventionally used in flow cytometry to fluorescently stain dead cells, for infarct size analysis after short periods of reperfusion. Forty-five rabbits were subjected to either 15 min, 2 h or 4.5 h of coronary artery occlusion without reperfusion, or to 15 min, 30 min and 2 h of coronary artery occlusion followed by 30 min, 1 h and 3 h of reperfusion. Fifteen min before terminating the experiment, PI was injected into the left atrium. Patent blue violet was used to delineate the area at risk. Following incubation in TTC, the area at risk was excised and cross sections obtained for microscopical infarct size quantification by PI fluorescence. PI fluorescence was absent after permanent occlusion and in control areas. Infarct sizes measured by TTC staining were significantly smaller after 1 h of reperfusion as compared to 3 h of reperfusion (30 min occlusion: 1+/-1 v 34+/-9%; P<0.05; 2 h occlusion: 9+/-6 v 47+/-8%; P<0.01). In contrast, infarct sizes determined by PI fluorescence reached values comparable to those measured by TTC staining or conventional histology after longer times of reperfusion already after 30 min of reperfusion (30 min occlusion: 35+/-16.5%; 2 h of occlusion: 61+/-8%). Therefore, after short times of reperfusion infarct size measurement by PI fluorescence is more reliable than by TTC staining.

摘要

通过氯化三苯基四氮唑(TTC)染色来描绘梗死面积取决于充分的再灌注。因此,我们评估了使用碘化丙啶(PI)的可能性,PI是一种常用于流式细胞术对死细胞进行荧光染色的试剂,用于短时间再灌注后的梗死面积分析。45只兔子接受了15分钟、2小时或4.5小时的冠状动脉闭塞且无再灌注,或者接受了15分钟、30分钟和2小时的冠状动脉闭塞,随后分别进行30分钟、1小时和3小时的再灌注。在实验结束前15分钟,将PI注入左心房。专利蓝紫用于描绘危险区域。在TTC中孵育后,切除危险区域并获取横截面,通过PI荧光对显微镜下的梗死面积进行定量。永久性闭塞后以及在对照区域均未观察到PI荧光。与再灌注3小时相比,再灌注1小时后通过TTC染色测量的梗死面积显著更小(闭塞30分钟:1±1%对34±9%;P<0.05;闭塞2小时:9±6%对47±8%;P<0.01)。相比之下,通过PI荧光测定的梗死面积在再灌注30分钟后,经过更长时间的再灌注,已经达到了与通过TTC染色或传统组织学测量的值相当的水平(闭塞30分钟:35±16.5%;闭塞2小时:61±8%)。因此,在短时间再灌注后,通过PI荧光测量梗死面积比通过TTC染色更可靠。

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