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Simultaneous Measurement of Cytoplasmic and SR Calcium during Modulation of Ryanodine Receptor Open Probability in Dog Ventricular Myocytes

Greensmith, David J.; Galli, Gina L.J; Morton, Michael J.; Pollard, Christopher E.; Trafford, Andrew W.; Eisner, David A.

Authors

Gina L.J Galli

Michael J. Morton

Christopher E. Pollard

Andrew W. Trafford

David A. Eisner



Abstract

We have previously found that, in rat ventricular myocytes, increasing ryanodine receptor open probability using low concentrations of caffeine had no maintained effect on the amplitude of systolic Ca. On application of caffeine, following an initial increase, systolic Ca returned to control levels in around 20 s and it was argued that this was due to a concurrent decrease in SR Ca. In the present study, we sought to obtain direct evidence for the involvement of a decrease of SR Ca in this transient response.
SR Ca was measured directly with Mag-Fura-2. Application of 0.5 mM caffeine initially caused a 197 % increase in the amplitude of systolic Ca. This was associated with a 874 % increase in the amplitude of SR Ca loss and a 328 and 178 % increase in the rate of systolic cytoplasmic Ca removal and SR Ca replenishment respectively. In sustained caffeine exposure, all these parameters returned to levels comparable to control, typically within 1 - 2 beats. During caffeine exposure, SR Ca content rapidly decreased within 1 - 2 beats to a new steady state level. All measured parameters recovered to control levels on removal of caffeine.
These data show, on RyR potentiation, following the initial increase, the secondary decrease of systolic Ca is due to a decrease in SR Ca.

Presentation Conference Type Conference Abstract
Conference Name The 57th Annual Meeting of the Biophysical Society
Start Date Feb 2, 2013
End Date Feb 6, 2013
Publication Date 2013-01
Deposit Date Jun 24, 2025
Journal Biophysical Journal
Print ISSN 0006-3495
Electronic ISSN 1542-0086
Publisher Biophysical Society
Peer Reviewed Peer Reviewed
Volume 104
Issue 2
Article Number 438A
DOI https://doi.org/10.1016/j.bpj.2012.11.2433