Key result
In a rabbit model of acute myocardial infarction, [(123)I]MIH microSPECT successfully delineated infarcts in vivo, achieving a high mean infarct-to-viable tissue activity ratio of 61/1 at 24 hours.
Why the study?
Does mono-[123I]iodohypericin microSPECT imaging allow for non-invasive detection and quantification of acute myocardial infarction in rabbit models?
Does mono-[123I]iodohypericin microSPECT imaging allow for non-invasive detection and quantification of acute myocardial infarction in rabbit models?
Mono-[123I]iodohypericin microSPECT is a suitable imaging modality for the in vivo visualization and quantification of acute myocardial infarction in preclinical models.
[(123)I]MIH microSPECT feasible for infarct visualization in rabbits; leaves open clinical translation pending human studies.
AIMS: Mono-[(123)I]iodohypericin ([(123)I]MIH) has been reported to have high avidity for necrosis. In the present study, by using rabbit models of acute myocardial infarction, we explored the suitability of [(123)I]MIH micro single photon emission computed tomography (microSPECT) for non-invasive visualization of myocardial infarcts in comparison with [(13)N]ammonia micro positron emission tomography (microPET) imaging, postmortem histomorphometry, and [(123)I]MIH autoradiography. METHODS AND RESULTS: Fourteen rabbits were divided into four groups. The left circumflex coronary artery was permanently occluded in group A (n = 3), reperfused by releasing the ligature after 15 min in group B (n = 3) or 90 min in group C (n = 6), or not occluded in group D (n = 2). Animals received [(13)N]ammonia microPET perfusion imaging 18 h after infarct induction followed by microSPECT imaging at 2-3.5, 9-11, and 22-24 h post injection (p.i.) of [(123)I]MIH. The cardiac images were assembled into polar maps for assessment of tracer uptake. Animals were sacrificed and the excised heart was sliced for autoradiography, triphenyl tetrazolium chloride, and haematoxylin-eosin staining. Using [(123)I]MIH microSPECT, infarcts were well delineated at 9 h p.i. Mean microSPECT infarct size was 38.8 and 32.7% of left ventricular area for groups A and C, respectively, whereas group B showed low uptake of [(123)I]MIH. Highest mean infarct/viable tissue activity ratio of 61/1 was obtained by autoradiography in group C animals at 24 h p.i. CONCLUSION: The study indicates the suitability of [(123)I]MIH for in vivo visualization of myocardial infarcts.
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Fonge et al. (2007) studied Acute myocardial infarction (n=14). [(123)I]MIH microSPECT vs. [(13)N]ammonia microPET, histomorphometry, and autoradiography was evaluated on Infarct size and tracer uptake. In a rabbit model of acute myocardial infarction, [(123)I]MIH microSPECT successfully delineated infarcts in vivo, achieving a high mean infarct-to-viable tissue activity ratio of 61/1 at 24 hours.
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