Literature DB >> 1316183

Steady-state availability of sodium channels. Interactions between activation and slow inactivation.

P C Ruben1, J G Starkus, M D Rayner.   

Abstract

Changes in holding potential (Vh), affect both gating charge (the Q(Vh) curve) and peak ionic current (the F(Vh) curve) seen at positive test potentials. Careful comparison of the Q(Vh) and F(Vh) distributions indicates that these curves are similar, having two slopes (approximately 2.5e for Vh from -115 to -90 mV and approximately 4e for Vh from -90 to -65 mV) and very negative midpoints (approximately -86 mV). Thus, gating charge movement and channel availability appear closely coupled under fully-equilibrated conditions. The time course by which channels approach equilibration was explored using depolarizing prepulses of increasing duration. The high slope component seen in the F(Vh) and Q(Vh) curves is not evident following short depolarizing prepulses in which the prepulse duration approximately corresponds to the settling time for fast inactivation. Increasing the prepulse duration to 10 ms or longer reveals the high slope, and left-shifts the midpoint to more negative voltages, towards the F(Vh) and Q(Vh) distributions. These results indicate that a separate slow-moving voltage sensor affects the channels at prepulse durations greater than 10 ms. Charge movement and channel availability remain closely coupled as equilibrium is approached using depolarizing pulses of increasing durations. Both measures are 50% complete by 50 ms at a prepulse potential of -70 mV, with proportionately faster onset rates when the prepulse potential is more depolarized. By contrast, charge movement and channel availability dissociate during recovery from prolonged depolarizations. Recovery of gating charge is considerably faster than recovery of sodium ionic current after equilibration at depolarized potentials. Recovery of gating charge at -140 mV, is 65% complete within approximately 100 ms, whereas less than 30% of ionic current has recovered by this time. Thus, charge movement and channel availability appear to be uncoupled during recovery, although both rates remain voltage sensitive. These data suggest that channels remain inactivated due to a separate process operating in parallel with the fast gating charge. We demonstrate that this behavior can be simulated by a model in which the fast charge movement associated with channel activation is electrostatically-coupled to a separate slow voltage sensor responsible for the slow inactivation of channel conductance.

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Year:  1992        PMID: 1316183      PMCID: PMC1260353          DOI: 10.1016/S0006-3495(92)81901-X

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  35 in total

1.  Structural parts involved in activation and inactivation of the sodium channel.

Authors:  W Stühmer; F Conti; H Suzuki; X D Wang; M Noda; N Yahagi; H Kubo; S Numa
Journal:  Nature       Date:  1989-06-22       Impact factor: 49.962

2.  Intramembrane charge movement in frog skeletal muscle fibres. Properties of charge 2.

Authors:  G Brum; E Rios
Journal:  J Physiol       Date:  1987-06       Impact factor: 5.182

3.  Slow sodium inactivation in Myxicola axons. Evidence for a second inactive state.

Authors:  C L Schauf; T L Pencek; F A Davis
Journal:  Biophys J       Date:  1976-07       Impact factor: 4.033

4.  Solute inaccessible aqueous volume changes during opening of the potassium channel of the squid giant axon.

Authors:  J Zimmerberg; F Bezanilla; V A Parsegian
Journal:  Biophys J       Date:  1990-05       Impact factor: 4.033

5.  Saxitoxin and tetrodotoxin. Electrostatic effects on sodium channel gating current in crayfish axons.

Authors:  S T Heggeness; J G Starkus
Journal:  Biophys J       Date:  1986-03       Impact factor: 4.033

6.  Identification of an intracellular peptide segment involved in sodium channel inactivation.

Authors:  P M Vassilev; T Scheuer; W A Catterall
Journal:  Science       Date:  1988-09-23       Impact factor: 47.728

7.  The steady-state distribution of gating charge in crayfish giant axons.

Authors:  M D Rayner; J G Starkus
Journal:  Biophys J       Date:  1989-01       Impact factor: 4.033

8.  Comparison between slow sodium channel inactivation in rat slow- and fast-twitch muscle.

Authors:  R L Ruff; L Simoncini; W Stühmer
Journal:  J Physiol       Date:  1987-02       Impact factor: 5.182

9.  A neutral amino acid change in segment IIS4 dramatically alters the gating properties of the voltage-dependent sodium channel.

Authors:  V J Auld; A L Goldin; D S Krafte; W A Catterall; H A Lester; N Davidson; R J Dunn
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

10.  The effects of external potassium and long duration voltage conditioning on the amplitude of sodium currents in the giant axon of the squid, Loligo pealei.

Authors:  W J Adelman; Y Palti
Journal:  J Gen Physiol       Date:  1969-11       Impact factor: 4.086

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  26 in total

1.  Slow recovery from inactivation regulates the availability of voltage-dependent Na(+) channels in hippocampal granule cells, hilar neurons and basket cells.

Authors:  R K Ellerkmann; V Riazanski; C E Elger; B W Urban; H Beck
Journal:  J Physiol       Date:  2001-04-15       Impact factor: 5.182

2.  A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivation.

Authors:  Y Y Vilin; E Fujimoto; P C Ruben
Journal:  Biophys J       Date:  2001-05       Impact factor: 4.033

3.  Structural determinants of slow inactivation in human cardiac and skeletal muscle sodium channels.

Authors:  Y Y Vilin; N Makita; A L George; P C Ruben
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

Review 4.  Mechanisms of closed-state inactivation in voltage-gated ion channels.

Authors:  Robert Bähring; Manuel Covarrubias
Journal:  J Physiol       Date:  2010-11-22       Impact factor: 5.182

5.  Slow inactivation of Na+ current and slow cumulative spike adaptation in mouse and guinea-pig neocortical neurones in slices.

Authors:  I A Fleidervish; A Friedman; M J Gutnick
Journal:  J Physiol       Date:  1996-05-15       Impact factor: 5.182

6.  Slow inactivation in human cardiac sodium channels.

Authors:  J E Richmond; D E Featherstone; H A Hartmann; P C Ruben
Journal:  Biophys J       Date:  1998-06       Impact factor: 4.033

7.  Impaired slow inactivation in mutant sodium channels.

Authors:  T R Cummins; F J Sigworth
Journal:  Biophys J       Date:  1996-07       Impact factor: 4.033

8.  A mutation in segment I-S6 alters slow inactivation of sodium channels.

Authors:  S Y Wang; G K Wang
Journal:  Biophys J       Date:  1997-04       Impact factor: 4.033

9.  Prolonged sodium channel inactivation contributes to dendritic action potential attenuation in hippocampal pyramidal neurons.

Authors:  H Y Jung; T Mickus; N Spruston
Journal:  J Neurosci       Date:  1997-09-01       Impact factor: 6.167

10.  Interaction between duration of activity and time course of recovery from slow inactivation in mammalian brain Na+ channels.

Authors:  A Toib; V Lyakhov; S Marom
Journal:  J Neurosci       Date:  1998-03-01       Impact factor: 6.167

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