Literature DB >> 12562930

Crucial role of sodium channel fast inactivation in muscle fibre inexcitability in a rat model of critical illness myopathy.

Mark M Rich1, Martin J Pinter.   

Abstract

Critical illness myopathy is an acquired disorder in which skeletal muscle becomes electrically inexcitable. We previously demonstrated that inactivation of Na+ channels contributes to inexcitability of affected fibres in an animal model of critical illness myopathy in which denervated rat skeletal muscle is treated with corticosteroids (steroid denervated; SD). Our previous work, however, did not address the relative importance of membrane depolarization versus a shift in the voltage dependence of fast inactivation in causing inexcitability. It also remained unknown whether changes in the voltage dependence of activation or slow inactivation play a role in inexcitability. In the current study we found that a hyperpolarizing shift in the voltage dependence of fast inactivation of Na+ channels is the principal factor underlying inexcitability in SD fibres. Although depolarization tends to decrease excitability, it is insufficient to account for inexcitability in SD fibres since many normal and denervated fibres retain normal excitability when depolarized to the same resting potentials as affected SD fibres. Changes in the voltage dependence of activation and slow inactivation of Na+ channels were also observed in SD fibres; however, the changes appear to increase rather than decrease excitability. These results highlight the importance of the change in fast inactivation in causing inexcitability of SD fibres.

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Year:  2003        PMID: 12562930      PMCID: PMC2342662          DOI: 10.1113/jphysiol.2002.035188

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  32 in total

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Authors:  Y Zhang; H A Hartmann; J Satin
Journal:  J Membr Biol       Date:  1999-10-01       Impact factor: 1.843

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Authors:  H Todt; S C Dudley; J W Kyle; R J French; H A Fozzard
Journal:  Biophys J       Date:  1999-03       Impact factor: 4.033

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Journal:  Acta Physiol Scand       Date:  1996-03

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

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Authors:  D E Featherstone; J E Richmond; P C Ruben
Journal:  Biophys J       Date:  1996-12       Impact factor: 4.033

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Journal:  J Physiol       Date:  1987-02       Impact factor: 5.182

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Journal:  J Physiol       Date:  1987-07       Impact factor: 5.182

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9.  Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5.

Authors:  S Bendahhou; T R Cummins; R W Kula; Y-H Fu; L J Ptácek
Journal:  Neurology       Date:  2002-04-23       Impact factor: 9.910

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Journal:  Am J Physiol       Date:  1977-03
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  51 in total

1.  Hyperpolarized shifts in the voltage dependence of fast inactivation of Nav1.4 and Nav1.5 in a rat model of critical illness myopathy.

Authors:  Gregory N Filatov; Mark M Rich
Journal:  J Physiol       Date:  2004-07-14       Impact factor: 5.182

2.  Excitability of the T-tubular system in rat skeletal muscle: roles of K+ and Na+ gradients and Na+-K+ pump activity.

Authors:  O B Nielsen; N Ørtenblad; G D Lamb; D G Stephenson
Journal:  J Physiol       Date:  2004-03-19       Impact factor: 5.182

Review 3.  [Intensive care unit-acquired weakness in the critically ill : critical illness polyneuropathy and critical illness myopathy].

Authors:  K Judemann; D Lunz; Y A Zausig; B M Graf; W Zink
Journal:  Anaesthesist       Date:  2011-10       Impact factor: 1.041

4.  A selective role for MRF4 in innervated adult skeletal muscle: Na(V) 1.4 Na+ channel expression is reduced in MRF4-null mice.

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Journal:  Gene Expr       Date:  2005

5.  Open-label trial of ranolazine for the treatment of myotonia congenita.

Authors:  W David Arnold; David Kline; Alan Sanderson; Ahmed A Hawash; Amy Bartlett; Kevin R Novak; Mark M Rich; John T Kissel
Journal:  Neurology       Date:  2017-07-14       Impact factor: 9.910

6.  Speeding the recovery from ultraslow inactivation of voltage-gated Na+ channels by metal ion binding to the selectivity filter: a foot-on-the-door?

Authors:  Julia Szendroedi; Walter Sandtner; Touran Zarrabi; Eva Zebedin; Karlheinz Hilber; Samuel C Dudley; Harry A Fozzard; Hannes Todt
Journal:  Biophys J       Date:  2007-08-24       Impact factor: 4.033

Review 7.  Diagnosis of acute neuropathies.

Authors:  Clarissa Crone; Christian Krarup
Journal:  J Neurol       Date:  2007-09-21       Impact factor: 4.849

8.  Role of Ca(2+) in injury-induced changes in sodium current in rat skeletal muscle.

Authors:  Gregory N Filatov; Martin J Pinter; Mark M Rich
Journal:  Am J Physiol Cell Physiol       Date:  2009-06-03       Impact factor: 4.249

9.  Review of Critical Illness Myopathy and Neuropathy.

Authors:  Starane Shepherd; Ayush Batra; David P Lerner
Journal:  Neurohospitalist       Date:  2016-08-23

10.  Permanent myopathy caused by mutation of SCN4A Metl592Val: Observation on myogenesis in vitro and on effect of basic fibroblast growth factor on the muscle.

Authors:  Yu Feng; Hong Wang; Xiao-Guang Luo; Yan Ren
Journal:  Neurosci Bull       Date:  2009-04       Impact factor: 5.203

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