Key result
Label-free optical readouts successfully monitored progressive collagen deposition and metabolic alterations in vivo up to 4 weeks post-myocardial infarction in rats.
Why the study?
The mechanisms of cardiac remodeling following myocardial infarction in infarcted and remote myocardium are not fully understood.
Does label-free optical monitoring detect structural and metabolic remodeling in the myocardium following infarction in a rat model?
Does label-free optical monitoring detect structural and metabolic remodeling in the myocardium following infarction in a rat model?
Label-free optical spectroscopy can monitor structural and metabolic cardiac remodeling in vivo following myocardial infarction, offering a potential tool for real-time tissue characterization.
Supports preclinical optical monitoring of post-MI remodeling in rats; leaves open clinical translation.
Cardiac remodeling following myocardial infarction (MI) involves structural and functional alterations in the infarcted and remote viable myocardium that can ultimately lead to heart failure. The underlying mechanisms are not fully understood and, following our previous study of the autofluorescence lifetime and diffuse reflectance signatures of the myocardium in vivo at 16 weeks post MI in rats [Biomed. Opt. Express6(2), 324 (2015)], we here present data obtained at 1, 2 and 4 weeks post myocardial infarction that help follow the temporal progression of these changes. Our results demonstrate that both structural and metabolic changes in the heart can be monitored from the earliest time points following MI using label-free optical readouts, not only in the region of infarction but also in the remote non-infarcted myocardium. Changes in the autofluorescence intensity and lifetime parameters associated with collagen type I autofluorescence were indicative of progressive collagen deposition in tissue that was most pronounced at earlier time points and in the region of infarction. In addition to significant collagen deposition in infarcted and non-infarcted myocardium, we also report changes in the autofluorescence parameters associated with reduced nicotinamide adenine (phosphate) dinucleotide (NAD(P)H) and flavin adenine dinucleotide (FAD), which we associate with metabolic alterations throughout the heart. Parallel measurements of the diffuse reflectance spectra indicated an increased contribution of reduced cytochrome c. Our findings suggest that combining time-resolved spectrofluorometry and diffuse reflectance spectroscopy could provide a useful means to monitor cardiac function in vivo at the time of surgery.
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Lagarto et al. (2019) studied Myocardial infarction. Label-free optical monitoring was evaluated on Structural and metabolic changes (collagen deposition, NAD(P)H, FAD, cytochrome c). Label-free optical readouts successfully monitored progressive collagen deposition and metabolic alterations in vivo up to 4 weeks post-myocardial infarction in rats.
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