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1 Departments of Veterinary and
Comparative Anatomy,
The objective was to determine the dynamics of
contractile processes from pressure responses to small-amplitude,
sinusoidal volume changes in the left ventricle of the beating heart.
Hearts were isolated from 14 anesthetized rabbits and paced at 1 beats/s. Volume was perturbed sinusoidally at four
frequencies ( f ) (25, 50, 76.9, and 100 Hz) and five amplitudes (0.50, 0.75, 1.00, 1.25, and 1.50% of baseline
volume). A prominent component of the pressure response occurred at the
f of perturbation [in-frequency
response,
(t)].
A model, based on cross-bridge mechanisms and containing both pre- and
postpower stroke states, was constructed to interpret
(t).
Model predictions were that
(t)
consisted of two parts: a part with an amplitude rising and falling in
proportion to the pressure around that which
(t)
occurred
[Pr(t)],
and a part with an amplitude rising and falling in proportion to the
derivative of
Pr(t)
with time. Statistical analysis revealed that both parts
were significant. Additional model predictions concerning response
amplitude and phase were also confirmed statistically. The model was
further validated by fitting simultaneously to all
(t) over the full range of f and
V in a
given heart. Residual errors from fitting were small
(R2 = 0.978) and
were not systematically distributed. Elaborations of the model to
include noncontractile series elastance and distortion-dependent cross-bridge detachment did not improve the ability to represent the
data. We concluded that the model could be used to identify cross-bridge rate constants in the whole heart from responses to 25- to
100-Hz sinusoidal volume perturbations.
cross-bridge model; cross-bridge detachment; cross-bridge power stroke; heart muscle
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