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December 4, 1987Science355 citations

Effect of Membrane Potential Changes on the Calcium Transient in Single Rat Cardiac Muscle Cells

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MCMark B. CannellJBJoshua R. BerlinWLW. Jonathan Lederer

Key Points

  • This research aims to clarify the relationship between membrane potential changes and calcium release in cardiac muscle cells.
  • Used voltage-clamp conditions to monitor intracellular calcium with fura-2 in single rat ventricular cells.

Structured PICO

P
Population
Single rat ventricular cells
I
Intervention
Membrane potential changes (depolarization and repolarization) under voltage-clamp conditions
O
Outcome
Changes in intracellular calcium monitored by the calcium indicator fura-2surrogate

Membrane potential changes directly regulate sarcoplasmic reticulum calcium release and the time course of the calcium transient in cardiac cells, independent of the calcium current.

Abstract

The mechanism that links membrane potential changes to the release of calcium from internal stores to cause contraction of cardiac cells is unclear. By using the calcium indicator fura-2 under voltage-clamp conditions, changes in intracellular calcium could be monitored in single rat ventricular cells while controlling membrane potential. The voltage dependence of the depolarization-induced increase in intracellular calcium was not the same as that of the calcium current (Isi), which suggests that only a small fraction of Isi is required to trigger calcium release from the sarcoplasmic reticulum. In addition, sarcoplasmic reticulum calcium release may be partly regulated by membrane potential, since repolarization could terminate the rise in intracellular calcium. Thus, changes in the action potential will have immediate effects on the time course of the calcium transient beyond those associated with its effects on Isi.

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Cite This Study

Cannell et al. (1987) studied this question.

synapsesocial.com/papers/6a20798acbc595e19031812dhttps://doi.org/10.1126/science.2446391
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