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Journal of Nuclear Medicine Vol. 43 No. 11 1557-1569
© 2002 by Society of Nuclear Medicine


Basic Science Investigations

Delineation of Hypoxia in Canine Myocardium Using PET and Copper(II)-Diacetyl-bis(N4-Methylthiosemicarbazone)

Jason S. Lewis, PhD1, Pilar Herrero, MS1, Terry L. Sharp1, John A. Engelbach1, Yasuhisa Fujibayashi, PhD, DMedSci2, Richard Laforest, PhD1, Attila Kovacs, MD1, Robert J. Gropler, MD1 and Michael J. Welch, PhD1

1 Division of Radiological Sciences, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri
2 Biomedical Imaging Research Center, Fukui Medical University, Matsuoka, Fukui, Japan

Copper(II)-diacetyl-bis(N4-methylthiosemicarbazone) (copper-ATSM) is a hypoxia-avid tracer for the selective identification of hypoxic tissue. Using canine models of hypoxic myocardium, we report our findings on *Cu-ATSM PET (*Cu is defined as either 60Cu, 61Cu, or 64Cu) for the delineation of ischemic and hypoxic myocardium. Methods: In protocol I, myocardial hypoxia was induced by global hypoxia (n = 3). In protocol II, myocardial ischemia was generated by occlusion of the left anterior descending coronary artery (n = 9). In protocol III, coronary artery stenosis was induced by a stenosis in the left anterior descending coronary artery (n = 4). PET dynamic data were acquired immediately after tracer injection. Tracer retention kinetics were analyzed using either monoexponential analysis (1/kmono) or a simple 2-compartment model (1/k4). Results: In protocol I, tracer retention in hypoxic myocardium was 2-fold greater than in normal myocardium, despite a 7-fold increase in blood flow (normal, 0.70 ± 0.42 mL·min-1·g-1; hypoxic, 4.94 ± 3.00 mL·min-1·g-1 [P < 0.005]). In protocol II, ~3 h after occlusion, retention of *Cu-ATSM within 20 min was greater in ischemic regions (myocardial blood flow, 0.28 ± 0.26 mL·min-1·g-1) than in normal tissue (myocardial blood flow, 0.52 ± 0.19 mL·min-1·g-1) (1/kmono, 40.72 ± 39.0 min vs. 26.69 ± 22.29 min [P < 0.05]; 1/k4, 6.85 ± 4.90 min vs. 3.51 ± 1.97 min [P < 0.05]). In selected dogs, tracer retention decreased at 24 h, suggesting the development of necrosis with no subsequent retention of *Cu-ATSM. In protocol III, dobutamine infusion after stenosis placement resulted in increased tracer retention consistent with hypoxia in the damaged regions. Conclusion: *Cu-ATSM PET has shown quantitative selective uptake in hypoxic myocardium within 20 min of tracer administration in 3 canine models of hypoxia.

Key Words: copper(II)-diacetyl-bis(N4-methylthiosemicarbazone) • imaging • ischemia • hypoxia




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