4.3 Article

Imaging assessment of cardioprotection mediated by a dodecafluoropentane oxygen-carrier administered during myocardial infarction

期刊

NUCLEAR MEDICINE AND BIOLOGY
卷 70, 期 -, 页码 67-77

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2019.01.004

关键词

Myocardial ischemia-reperfusion; Dodecafluoropentane perfluorocarbon emulsion; Phosphatidylethanolamine; Tc-99m-Duramycin; Cell death imaging

资金

  1. Translational Imaging Program Project Stimulus (TIPPS) Award of the University of Arizona
  2. National Institutes of Health (NIH) [NIBIB P41EB002035, NHLBI R01HL136603, NHLBI RO1HL138242]

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Introduction: The objective of this study was to investigate the cardioprotective effects of a dodecafluoropentane (DDFP)-based perfluorocarbon emulsion (DDFPe) as an artificial carrier for oxygen delivery to ischemic myocardium, using Tc-99m-duramycin SPELT imaging. Methods: Rat hearts with Ischemia-reperfusion (I/R) was prepared by coronary ligation for 45-min followed by reperfusion. The feasibility of Tc-99m-duramycin in detecting myocardial I/R injury and its kinetic profile were first verified in the ischemic hearts with 2-h reperfusion (n = 6). DDFPe (0.6 mL/kg) was intravenously administered at 10 min after coronary ligation in fifteen rats and saline was given in thirteen rats as controls. Tc-99m-duramycin SPELT images were acquired in the DDFPe-treated hearts and saline controls at 2-h (DDFPe-2 h, n = 7 and Saline-2 h, n = 6) or 24-h (DDFPe-24 h, n = 8 and Saline-24 h, n = 7) of reperfusion. Results: SPECT images, showing hot-spot Tc-99m-duramycin uptake in the ischemic myocardium, exhibited significantly lower radioactive retention and smaller hot-spot size in the DDFPe-2 h and DDFPe-24 h hearts compared to controls. The infarcts in the Saline-24 h hearts extended significantly relative to measurements in the Saline-2 h. The extension of infarct size did not reach a statistical difference between the DDFPe-2 h and DDFPe-24 h hearts. Ex vivo measurement of Tc-99m-duramycin activity (%ID/g) was lower in the ischemic area of DDFPe-2 h and DDFPe-24 h than that of the Saline-2 h and Saline-24 h hearts (P < 0.05). The area of injured myocardium, delineated by the uptake of Tc-99m-duramycin, extended more substantially outside the infarct zone in the controls. Conclusions: Significant reduction in myocardial I/R injury, as assessed by Tc-99m-duramycin cell death imaging and histopathological analysis, was induced by DDFPe treatment after acute myocardial ischemia. Tc-99m-duramycin imaging can reveal myocardial cell death in ischemic hearts and may provide a tool for the noninvasive assessment of cardioprotective interventions. (C) 2019 Elsevier Inc. All rights reserved.

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