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Department of Kinesiology and Applied Physiology and The University of Colorado Cardiovascular Institute, University of Colorado at Boulder, Boulder, Colorado 80309
The effects of
endurance run training on
Na+-dependent
Ca2+ regulation in rat left
ventricular myocytes were examined. Myocytes were isolated from
sedentary and trained rats and loaded with fura 2. Contractile dynamics
and fluorescence ratio transients were recorded during electrical
pacing at 0.5 Hz, 2 mM extracellular Ca2+ concentration, and 29°C.
Resting and peak cytosolic Ca2+
concentration
([Ca2+]c)
did not change with exercise training. However, resting and peak
[Ca2+]c
increased significantly in both groups during 5 min of continuous pacing, although diastolic
[Ca2+]c
in the trained group was less susceptible to this elevation of
intracellular Ca2+. Run training
also significantly reduced the rate of
[Ca2+]c
decay during relaxation. Myocytes were then exposed to 10 mM caffeine
in the absence of external Na+ or
Ca2+ to trigger sarcoplasmic
reticular Ca2+ release and to
suppress cellular Ca2+ efflux.
This maneuver elicited an elevated steady-state
[Ca2+]c.
External Na+ was then added, and
the rate of
[Ca2+]c
clearance was determined. Run training significantly reduced the rate
of Na+-dependent clearance of
[Ca2+]c
during the caffeine-induced contractures. These data demonstrate that
the removal of cytosolic Ca2+ was
depressed with exercise training under these experimental conditions
and may be specifically reflective of a training-induced decrease in
the rate of cytosolic Ca2+ removal
via
Na+/Ca2+
exchange and/or in the amount of
Ca2+ moved across the sarcolemma
during a contraction.
sodium/calcium exchange; fura 2; caffeine; sarcolemma; sarcoplasmic reticulum
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