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Detection of Myocardial Ischemia-Reperfusion Injury Using a Fluorescent Near-Infrared Zinc(II)-Dipicolylamine Probe and 99mTc Glucarate

机译:使用心肌缺血再灌注损伤的检测荧光近红外锌(II)-Dipicolylamine探针与99mTc葡糖

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摘要

A fluorescent zinc 2,2′-dipicolylamine coordination complex PSVue®794 (probe 1) is known to selectively bind to phosphatidylserine exposed on the surface of apoptotic and necrotic cells. In this study, we investigated the cell death targeting properties of probe 1 in myocardial ischemia-reperfusion injury. A rat heart model of ischemia-reperfusion was used. Probe 1, control dye, or 99mTc glucarate was intravenously injected in rats subjected to 30-minute and 5-minute myocardial ischemia followed by 2-hour reperfusion. At 90 minutes or 20 hours postinjection, myocardial uptake was evaluated ex vivo by fluorescence imaging and autoradiography. Hematoxylin-eosin and cleaved caspase-3 staining was performed on myocardial sections to demonstrate the presence of ischemiareperfusion injury and apoptosis. Selective accumulation of probe 1 could be detected in the area at risk up to 20 hours postinjection. Similar topography and extent of uptake of probe 1 and 99mTc glucarate were observed at 90 minutes postinjection. Histologic analysis demonstrated the presence of necrosis, but only a few apoptotic cells could be detected. Probe 1 selectively accumulates in myocardial ischemia-reperfusion injury and is a promising cell death imaging tool.
机译:已知一种荧光锌2,2​​'-二聚溶胶胺配位复合PSVUE794(探针1),可选择性地结合在凋亡和坏死细胞表面上暴露的磷脂酰丝氨酸。在该研究中,我们研究了探针1在心肌缺血再灌注损伤中的细胞死亡靶向性质。使用了缺血再灌注的大鼠心脏模型。探针1,控制染料或 99m孔静脉内注射到30分钟和5分钟的心肌缺血后的大鼠中,然后再灌注2小时。在发布90分钟或20小时,通过荧光成像和放射自显影评估MECARDARDIAL摄取。在心肌切片上进行苏木精 - 曙红和切割的Caspase-3染色,以证明存在耐血液灌注损伤和凋亡。可以在危险面积上检测到危机1的选择性累积,高达20小时推出。在90分钟后,在90分钟内观察到类似的地形和摄取探针1和 99m Tc葡萄糖。组织学分析证明了坏死的存在,但只能检测到一些凋亡细胞。探针1在心肌缺血再灌注损伤中选择性地积累,并且是一个有前途的细胞死亡成像工具。

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