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  • Title: Identical unitary current amplitude and Ca(2+) block of cardiac Na channel before and during beta-adrenergic stimulation.
    Author: Hirano Y, Hiraoka M.
    Journal: Jpn J Physiol; 2001 Dec; 51(6):679-85. PubMed ID: 11846958.
    Abstract:
    We examined the possibility of Ca(2+) permeation through cardiac Na channels ("slip mode conductance") by an analysis of the voltage-dependent block of Na channels by Ca(2+). A Ca(2+) block of Na channels was evident in rat and guinea pig ventricular myocytes during cell-attached single channel recordings with a physiological ionic environment (140 mM Na(+) and 1 to 10 mM Ca(2+) in the pipette solution). Increasing external Ca(2+) concentration ([Ca(2+)](o)) in the pipette solution reduced the unitary current amplitude predominantly at negative potentials. With [Ca(2+)](o) > 1 mM, unitary current amplitude did not increase at potentials negative to -40 mV in spite of augmented driving forces. The application of 5 microM isoproterenol potentiated the single channel activity elicited by depolarizing pulses from the holding potential of -120 mV, indicating that the channels in the patch under examination were modified by protein kinase A (PKA) stimulation. Increased activity was also confirmed with veratridine-modified Na channels, where channel openings were markedly prolonged. In either case, isoproterenol-induced potentiation neither reduced nor altered the properties of Ca(2+) block of cardiac Na channels, as evidenced by the stable unitary current amplitudes at potential levels from -60 to -20 mV. These results indicate that interactions among Na(+), Ca(2+), and the channel molecule were not modified with respect to permeation properties. They therefore argue against the "slip mode" concept of classical cardiac Na channel if a general concept of ion permeation through "multi-ion pores" is applicable to determine the ionic selectivity of Na channels.
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