F. Urthaler et al., BEAT-TO-BEAT MEASUREMENTS OF [CA2-MUSCLE AFTER CHEMICAL LOADING OF AEQUORIN(](I) AND FORCE IN FERRET CARDIAC), The American journal of physiology, 265(6), 1993, pp. 30001703-30001710
This communication reports the development of a modified procedure for
chemical loading of aequorin in small multicellular cardiac preparati
ons, with special emphasis directed toward the implementation of a new
method for computer-controlled low-photon counting and digital proces
sing and analysis of the data to obtain intracellular Ca2+ concentrati
on ([Ca2+]i). In eight ferret right ventricular trabeculae, we measure
d the mechanical performance and found that, at 1.25 mM extracellular
Ca2+ concentration ([Ca2+]o), resting tension, developed tension, and
time to peak tension were unchanged by the loading procedure. Estimate
d resting and peak systolic [Ca2+]i were 299 +/- 65 and 766 +/- 131 nM
, respectively. Thirty minutes after raising the [Ca2+]o to 5 mM, ther
e was a robust increase in mechanical performance, with peak systolic
[Ca2+]i averaging 1,218 +/- 222 nM. The diastolic [Ca2+]i remained unc
hanged. In four other trabeculae, exposure to a low-Na+-containing sup
erfusate demonstrated a remarkable beat-to-beat correspondence of incr
eases in diastolic [Ca2+]i and resting tensions. The same beat-to-beat
concordance was also observed between the rapidly changing amplitudes
of peak [Ca2+]i and developed tension. In additional experiments, sim
ultaneous recordings of [Ca2+]i and force transients were obtained dur
ing rapid pace pause maneuvers. These studies showed distinct and quan
tifiable fluctuations of [Ca2+]i in a 1:1 relation to the mechanical r
ecord to a frequency of at approximately 300 beats/min. These results
demonstrate that beat-to-beat measurements of [Ca2+]i and tension tran
sients can be obtained with good resolution in multicellular cardiac p
reparations.