Abstract
1. Confocal Ca$^2+$ imaging was used to measure spontaneous release
events (Ca$^2+$ sparks) in fluo-3-loaded isolated rat ventricular
myocytes. 2. The microscopic Ca$^2+$ release flux underlying
Ca$^2+$ sparks was derived by adapting the methods used previously
to describe macroscopic Ca$^2+$ release from cell-averaged Ca$^2+$
transients. 3. The magnitude of the local release fluxes varied from
2 to 5 microM ms-1, depending on SR Ca$^2+$ loading conditions.
Following spontaneous activation, the release flux rapidly decayed
(tau = 6-12 ms). The rate of termination of release flux was found
to be directly related to the magnitude of the flux (r2 = 0.88).
4. The rate of termination of local release flux was slowed in the
presence of FK506, a compound that is known to reduce inactivation
of SR Ca$^2+$ channels in vitro. 5. These results suggest that
termination of release flux during sparks is not due to a spontaneous
stochastic decay process or local depletion of Ca$^2+$ from the
SR, but rather involves an active extinguishing mechanism such as
Ca$^2+$-dependent inactivation or adaptation.
- 9508828
- algorithms,
- aniline
- animals,
- calcium
- calcium,
- cells,
- channels,
- chemical,
- compounds,
- confocal,
- cultured,
- dyes,
- fluorescent
- gov't,
- heart
- heart,
- kinetics,
- microscopy,
- models,
- non-u.s.
- of
- p.h.s.,
- rats,
- reproducibility
- research
- results,
- reticulum,
- sarcoplasmic
- sprague-dawley,
- support,
- tacrolimus,
- u.s.
- ventricles,
- xanthenes,
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