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November 1, 1994AJP Heart and Circulatory Physiology41 citations

L-type calcium current in rod- and spindle-shaped myocytes isolated from rabbit atrioventricular node

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JHJules C. HancoxALA J Levi

Structured PICO

P
Population
Rod- and spindle-shaped myocytes isolated from the rabbit atrioventricular node
I
Intervention
Electrophysiological characterization using voltage clamps and pharmacological blockade (nifedipine 2-20 microM, cadmium 100-200 microM, manganese 1 mM)
O
Outcome
Properties of L-type calcium current (ICa) including activation, inactivation, and current densitysurrogate

L-type calcium current is largely responsible for the action potential upstroke in rabbit atrioventricular node myocytes.

Abstract

The atrioventricular node (AVN) is vital to normal cardiac function. The present report describes the properties of L-type calcium current (ICa) in rod- and spindle-shaped myocytes isolated from the rabbit AVN. With depolarizing voltage clamps from a holding potential of -40 mV, a rapidly activating ICa was observed, which peaked at +10 mV in most cells and exhibited a "bell-shaped" current-voltage relation. ICa was abolished by nifedipine (2-20 microM) and cadmium (100-200 microM) and was greatly reduced by manganese (1 mM). At +10 mV, time to peak ICa was 3.3 +/- 0.15 (SE) ms (n = 12) and ICa current density was 9.3 +/- 1.2 pA/pF (n = 9). Steady-state activation and inactivation curves for ICa showed half-maximal activation at -3.6 mV slope factor (k) = 6.6 mV and half-maximal inactivation at -25.8 mV (k = 6.5 mV). The time course of decay of ICa during a depolarizing pulse was voltage dependent and biexponential. The time course of recovery of ICa from inactivation was also biexponential (with two time constants tau 1 = 194.7 and tau 2 = 907.4 ms). Under current clamp, spontaneous action potentials from AVN cells were blocked by nifedipine as well as by cadmium, suggesting that L-type ICa was largely responsible for the action potential upstroke.

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Cite This Study

Hancox et al. (1994) studied this question.

synapsesocial.com/papers/6a86c8643a1d8ec5fdd3be06https://doi.org/10.1152/ajpheart.1994.267.5.h1670
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

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