Literature DB >> 11808773

Voltage-clamp analysis of membrane currents and excitation-contraction coupling in a crustacean muscle.

T Weiss1, C Erxleben, W Rathmayer.   

Abstract

A single fibre preparation from the extensor muscle of a marine isopod crustacean is described which allows the analysis of membrane currents and simultaneously recorded contractions under two-electrode voltage-clamp conditions. We show that there are three main depolarisation-gated currents, two are outward and carried by K+, the third is an inward Ca2+ current, I(Ca). Normally, the K+ currents which can be isolated by using K+ channel blockers, mask I(Ca). I(Ca) activates at potentials more positive than -40 mV, is maximal around 0 mV, and shows strong inactivation at higher depolarisation. Inactivation depends on current rather than voltage. Ba2+, Sr2+ and Mg2+ can substitute for Ca2+. Ba2+ currents are about 80% larger than Ca2+ currents and inactivate little. The properties of I(Ca) characterise it as a high threshold L-type current. The outward current consists primarily of a fast, transient A current, I(K(A)) and a maintained, delayed rectifier current, I(K(V)). In some fibres, a small Ca2+-dependent K+ current is also present. I(K(A)) activates fast at depolarisation above -45 mV, shows pronounced inactivation and is almost completely inactivated at holding potentials more positive than -40 mV. I(K(A)) is half-maximally blocked by 70 microM 4-aminopyridine (4-AP), and 70 mM tetraethylammonium (TEA). I(K(V)) activates more slowly, at about -30 mV, and shows no inactivation. It is half-maximally blocked by 2 mM TEA but rather insensitive to 4-AP. Physiologically, the two K+ currents prevent all-or-nothing action potentials and determine the graded amplitude of active electrical responses and associated contractions. Tension development depends on and is correlated with depolarisation-induced Ca2+ influx mediated by I(Ca). The voltage dependence of peak tension corresponds directly to the voltage dependence of the integrated I(Ca). The threshold potential for contraction is at about -38 mV. Peak tension increases with increasing voltage steps, reaches maximum at around 0 mV, and declines with further depolarisation.

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Year:  2001        PMID: 11808773     DOI: 10.1023/a:1013154612985

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  59 in total

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Authors:  R Levi; L J DeFelice
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Authors:  R D Keynes; E Rojas; R E Taylor; J Vergara
Journal:  J Physiol       Date:  1973-03       Impact factor: 5.182

7.  Characterization of the membrane ion currents of a model molluscan muscle, the accessory radula closer muscle of Aplysia californica. II. Depolarization-activated K currents.

Authors:  V Brezina; C G Evans; K R Weiss
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Review 8.  Barnacle muscle: Ca2+, activation and mechanics.

Authors:  C C Ashley; P J Griffiths; T J Lea; I P Mulligan; R E Palmer; S J Simnett
Journal:  Rev Physiol Biochem Pharmacol       Date:  1993       Impact factor: 5.545

9.  Resolution and pharmacological analysis of the voltage-dependent calcium channels of Drosophila larval muscles.

Authors:  M L Gielow; G G Gu; S Singh
Journal:  J Neurosci       Date:  1995-09       Impact factor: 6.167

10.  Voltage-activated currents in somatic muscle of the nematode parasite Ascaris suum.

Authors:  R J Martin; P Thorn; K A Gration; I D Harrow
Journal:  J Exp Biol       Date:  1992-12       Impact factor: 3.312

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  3 in total

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3.  Synaptic Dynamics Convey Differential Sensitivity to Input Pattern Changes in Two Muscles Innervated by the Same Motor Neurons.

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