Key result
The logistic function model was significantly superior to the monoexponential function for fitting [Ca2+]i declines and relaxation force curves in rabbit and mouse papillary muscles.
Why the study?
Does a logistic function provide a better fit than a monoexponential function for the decay of Ca2+ transient and isometric relaxation force curves in rabbit and mouse papillary muscles?
Does a logistic function provide a better fit than a monoexponential function for the decay of Ca2+ transient and isometric relaxation force curves in rabbit and mouse papillary muscles?
The logistic function more reliably characterizes myocardial intracellular calcium decline and relaxation force curves than the conventional monoexponential function, irrespective of animal species.
May improve Ca2+ transient modeling in animal studies; leaves open human validation.
A decrease in myocardial intracellular calcium concentration ([Ca(2+)](i)) precedes relaxation, and a monoexponential function is typically used for fitting the decay of the Ca(2+) transient. However, a logistic function has been shown to be a better fit for the relaxation force curve, compared to the conventional monoexponential function. In the present study, we compared the logistic and monoexponential functions for fitting the [Ca(2+)](i) declines, which were measured using the aequorin method, and isometric relaxation force curves at 4 different onsets: the minimum time-derivative of [Ca(2+)](i) (d[Ca(2+)](i)/dt (min)) and force (dF/dt(min)), and the 10%, 20% and 30% lower [Ca(2+)](i) levels and forces over the data-sampling period in 7 isolated rabbit right ventricular and 15 isolated mouse left ventricular papillary muscles. Logistic functions were significantly superior for fitting the [Ca(2+)] (i) declines and relaxation force curves, compared to monoexponential functions. Changes in the normalized logistic [Ca(2+)] (i) decline and relaxation force time constants at the delayed onsets relative to their 100% values at d[Ca(2+)] (i)/dt(min) and dF/dt(min) were significantly smaller than the changes in the normalized monoexponential time constants. The ratio of the logistic relaxation force time constant relative to the logistic [Ca(2+)](i) decline time constant was significantly smaller in mouse than in rabbit. We conclude that the logistic function more reliably characterizes the [Ca(2+)](i) decline and relaxation force curve at any onset, irrespective of animal species. Simultaneous analyses using the logistic model for decay of the Ca(2+) transient and myocardial lusitropism might be a useful strategy for analysis of species-specific myocardial calcium handling.
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Mizuno et al. (2007) studied Myocardial relaxation and calcium handling (n=22). Logistic function model vs. Monoexponential function model was evaluated on Goodness of fit (correlation coefficient and residual mean squares) for [Ca2+]i declines and relaxation force curves (p=<0.05). The logistic function model was significantly superior to the monoexponential function for fitting [Ca2+]i declines and relaxation force curves in rabbit and mouse papillary muscles.
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