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新型荧光探针 PSVue 794 在大鼠大脑中动脉闭塞再灌注模型中对脑梗死的体内成像。

In vivo imaging of brain infarct with the novel fluorescent probe PSVue 794 in a rat middle cerebral artery occlusion-reperfusion model.

机构信息

Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA 19140, USA.

出版信息

Mol Imaging. 2013 Jan-Feb;12(1):8-16.

PMID:23348787
Abstract

The utility of PSVue 794 (PS794), a near-infrared fluorescent dye conjugated to a bis[zinc (II)-dipicolylamine] (Zn-DPA) targeting moiety, in imaging brain infarct was assessed in a rat middle cerebral artery occlusion-reperfusion model. Following reperfusion, 1 mM PS794 solution was administered intravenously via a tail vein. Fluorescence images were captured between 6 to 72 hours postinjection using a LI-COR Biosciences Pearl Imaging System. Strong fluorescence signals, which may represent the infarct core, were detected in the right hemisphere, ipsilateral to the injured site, and weaker signals in areas surrounding the core. In ischemia-reperfusion rats injected with a control dye not linked to a targeting agent, fluorescence was distributed diffusely throughout the brain. To address the issue of whether Zn-DPA targets apoptotic/necrotic cells, HT22 mouse hippocampal neurons were cultured in either Dulbecco's Modified Eagle's Medium, serum-deprived medium, Hank's Balanced Salt Solution, or L-glutamate (10 mM)-containing medium for up to 33 hours. Cells were then double-labeled with PSVue 480 (Zn-DPA conjugated to fluorescein isothiocyanate) and propidium iodide, which labels necrotic cells. Microscopic examination revealed that PS480 targeted apoptotic and necrotic cells. The result indicates that PS794 is applicable to in vivo imaging of brain infarct and that Zn-DPA selectively targets apoptotic/necrotic cells.

摘要

PSVue 794(PS794)是一种近红外荧光染料,与双[锌(II)-二吡啶甲酰胺](Zn-DPA)靶向部分缀合,用于评估在大鼠大脑中动脉闭塞再灌注模型中成像脑梗死的效用。再灌注后,通过尾静脉静脉内给予 1mM PS794 溶液。在注射后 6 至 72 小时使用 LI-COR Biosciences Pearl 成像系统捕获荧光图像。在受伤部位对侧的右半球检测到强烈的荧光信号,可能代表梗死核心,而核心周围区域的信号较弱。在注射未与靶向剂连接的对照染料的缺血再灌注大鼠中,荧光在整个大脑中弥散分布。为了解决 Zn-DPA 是否靶向凋亡/坏死细胞的问题,将 HT22 小鼠海马神经元在含有胎牛血清的 DMEM 培养基、无血清培养基、Hank's 平衡盐溶液或含有 10mM L-谷氨酸的培养基中培养长达 33 小时。然后用 PSVue 480(与荧光素异硫氰酸酯缀合的 Zn-DPA)和碘化丙啶对细胞进行双重标记,碘化丙啶标记坏死细胞。显微镜检查显示 PS480 靶向凋亡和坏死细胞。结果表明 PS794 适用于脑梗死的体内成像,并且 Zn-DPA 选择性地靶向凋亡/坏死细胞。

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