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In Vivo Imaging of Brain Infarct with the Novel Fluorescent Probe PSVue 794 in a Rat Middle Cerebral Artery Occlusion-Reperfusion Model

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机构: [1]Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19140 USA; [2]Temple Univ, Sch Med, Dept Neurol, Philadelphia, PA 19140 USA; [3]Capital Med Univ, Dept Neurosurg, Beijing Tiantan Hosp, Beijing 100050, Peoples R China; [4]Natl Hlth Res Inst, Inst Biotechnol & Pharmaceut Res, Zhunan, Taiwan; [5]Mol Targeting Technol Inc, W Chester, PA USA; [6]Temple Univ, Sch Med, Dept Pharmacol, 3420 N Broad St, Philadelphia, PA 19140 USA
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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.

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出版当年[2012]版:
大类 | 3 区 生物
小类 | 2 区 核医学 3 区 生化研究方法
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 生化研究方法 4 区 核医学
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出版当年[2011]版:
Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q2 BIOCHEMICAL RESEARCH METHODS
最新[2023]版:
Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q3 BIOCHEMICAL RESEARCH METHODS

影响因子: 最新[2023版] 最新五年平均 出版当年[2011版] 出版当年五年平均 出版前一年[2010版] 出版后一年[2012版]

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第一作者机构: [1]Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19140 USA; [2]Temple Univ, Sch Med, Dept Neurol, Philadelphia, PA 19140 USA; [3]Capital Med Univ, Dept Neurosurg, Beijing Tiantan Hosp, Beijing 100050, Peoples R China; [4]Natl Hlth Res Inst, Inst Biotechnol & Pharmaceut Res, Zhunan, Taiwan; [5]Mol Targeting Technol Inc, W Chester, PA USA; [6]Temple Univ, Sch Med, Dept Pharmacol, 3420 N Broad St, Philadelphia, PA 19140 USA
通讯作者:
通讯机构: [1]Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19140 USA; [2]Temple Univ, Sch Med, Dept Neurol, Philadelphia, PA 19140 USA; [6]Temple Univ, Sch Med, Dept Pharmacol, 3420 N Broad St, Philadelphia, PA 19140 USA
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