Quantifying Acute Myocardial Injury Using Ratiometric Fluorometry
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biomedical measurement
cardiology
cellular biophysics
diseases
fluorescence
muscle
patient treatment
acute myocardial injury
cell death
cyclosporine A
flavoprotein
fluorescence
ischemia
mitochondrial dysfunction
myocardial infarction
myocardial salvage
nicotinamide adenine dinucleotide
ratiometric fluorometry
reperfusion therapy
time 3 h
time 30 min
Apoptosis
fluorometery
mitochondrial disruption
mitochondrial redox state
myocardial infarction
myocardial reperfusion injury
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Abstract
Early reperfusion is the best therapy for myocardial infarction (MI). Effectiveness, however, varies significantly between patients and has implications for long-term prognosis and treatment. A technique to assess the extent of myocardial salvage after reperfusion therapy would allow for high-risk patients to be identified in the early post-MI period. Mitochondrial dysfunction is associated with cell death following myocardial reperfusion and can be quantified by fluorometry. Therefore, we hypothesized that variations in the fluorescence of mitochondrial nicotinamide adenine dinucleotide (NADH) and flavoprotein (FP) can be used acutely to predict the degree of myocardial injury. Thirteen rabbits had coronary occlusion for 30 min followed by 3 h of reperfusion. To produce a spectrum of infarct sizes, six animals were infused cyclosporine A prior to ischemia. Using a specially designed fluorometric probe, NADH and FP fluorescence were measured in the ischemic area. Changes in NADH and FP fluorescence, as early as 15 min after reperfusion, correlated with postmortem assessment infarct size (r=0.695, p<0.01). This correlation strengthened with time (r=0.827, p<0.01 after 180 min). Clinical application of catheter-based myocardial fluorometry may provide a minimally invasive technique for assessing the early response to reperfusion therapy.