Voltage-Gated and Ca2+-Activated Conductances Mediating and Controlling Graded Electrical Activity in Crayfish Muscle

Author:

Araque Alfonso1,Marchand Alain2,Buño Washington1

Affiliation:

1. Instituto Cajal, Consejo Superior de Investigaciones Cientı́ficas, E-28002 Madrid, Spain; and

2. Laboratoire de Neurobiologie et Mouvements, Centre National de la Recherche Scientifique, F-13402 Marseille, France

Abstract

Araque, Alfonso, Alain Marchand, and Washington Buño. Voltage-gated and Ca2+-activated conductances mediating and controlling graded electrical activity in crayfish muscle. J. Neurophysiol. 79: 2338–2344, 1998. Crayfish opener muscle fibers provide a unique preparation to quantitatively evaluate the relationships between the voltage-gated Ca2+ ( I Ca) and Ca2+-activated K+ ( I K(Ca)) currents underlying the graded action potentials (GAPs) that typify these fibers. I Ca, I K(Ca), and the voltage-gated K+ current ( I K) were studied using two-electrode voltage-clamp applying voltage commands that simulated the GAPs evoked in current-clamp conditions by 60-ms current pulses. This methodology, unlike traditional voltage-clamp step commands, provides a description of the dynamic aspects of the interaction between different conductances participating in the generation of the natural GAP. The initial depolarizing phase of the GAP was due to activation of the I Ca on depolarization above approximately −40 mV. The resulting Ca2+ inflow induced the activation of the fast I K(Ca) (<3 ms), which rapidly repolarized the fiber (<6 ms). Because of its relatively slow activation, the contribution of I K to the GAP repolarization was delayed. During the final steady GAP depolarization I Ca and I K(Ca) were simultaneously activated with similar magnitudes, whereas I K aided in the control of the delayed sustained response. The larger GAPs evoked by higher intensity stimulations were due to the increase in I Ca. The resulting larger Ca2+ inflow increased I K(Ca), which acted as a negative feedback that precisely controlled the fiber's depolarization. Hence I K(Ca) regulated the Ca2+-inflow needed for the contraction and controlled the depolarization that this Ca2+ inflow would otherwise elicit.

Publisher

American Physiological Society

Subject

Physiology,General Neuroscience

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