Article,

Termination of Ca$^2+$ release during Ca$^2+$ sparks in rat ventricular myocytes.

, , and .
J. Physiol., (March 1998)

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.

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