Although a considerable number of studies have characterized inactivation and facilitation of macroscopic L-type Ca2+ channel currents, the single channel properties underlying these important regulatory processes have only rarely been examined using Ca2+ ions. We have compared unitary L-type Ca2+ channel currents recorded with a low concentration of Ca2+ ions with those recorded with Ba2+ ions to elucidate the ionic dependence of the mechanisms responsible for the prepulse-dependent modulation of Ca2+ channel gating kinetics. Conditioning prepulses were applied across a wide range of voltages to examine their effects on the subsequent Ca2+ channel activity, recorded at a constant test potential. All recordings were made in the absence of any Ca2+ channel agonists. Moderate-depolarizing prepulses resulted in a decrease in the probability of opening of the Ca2+ channels during subsequent test voltage steps (inactivation), the extent of which was more dramatic with Ca2+ ions than Ba2+ ions. Facilitation, or increase of the average probability of opening with strong predepolarization, was due to long-duration mode 2 openings with Ca2+ ions and Ba2+ ions, despite a decrease in Ca2+ channel availability (inactivation) under these conditions. The degree of both prepulse-induced inactivation and facilitation decreased with increasing Ba2+ ion concentration. The time constants (and their proportions) describing the distributions of Ca2+ channel open times (which reflect mode switching) were also prepulse-, and ion-dependent. These results support the hypothesis that both prior depolarization and the nature and concentration of permeant ions modulate the gating properties of cardiac L-type Ca2+ channels.
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Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
Navedo, Manuel F.
Cheng, Edward P.
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Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
Cheng, Edward P.
Yuan, Can
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Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
Yuan, Can
Votaw, Scott
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Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
Votaw, Scott
Molkentin, Jeffery D.
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Howard Hughes Med Inst, Cincinnati, OH USA
Childrens Hosp Med Ctr Mol Cardiovasc Biol, Cincinnati, OH USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
Molkentin, Jeffery D.
Scott, John D.
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Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
Univ Washington, Dept Pharmacol, Seattle, WA 98195 USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
Scott, John D.
Santana, Luis F.
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Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USAUniv Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA