Crucial Role of Sodium Channel Fast Inactivation in Muscle Fibre Inexcitability in a Rat Model of Critical Illness Myopathy

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.

[1]  D. K. Berg,et al.  INCREASED EXTRAJUNCTIONAL ACETYLCHOLINE SENSITIVITY PRODUCED BY CHRONIC POST-SYNAPTIC NEUROMUSCULAR BLOCKADE BY DARWIN K. BERG* AND ZACH W. HALL , 2005 .

[2]  W. Almers,et al.  Effect of glucocorticoid treatment on the excitability of rat skeletal muscle , 1982, Pflügers Archiv.

[3]  S. Bendahhou,et al.  Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5 , 2002, Neurology.

[4]  S. Dib-Hajj,et al.  Glycosylation Alters Steady-State Inactivation of Sodium Channel Nav1.9/NaN in Dorsal Root Ganglion Neurons and Is Developmentally Regulated , 2001, The Journal of Neuroscience.

[5]  H. Fozzard,et al.  The Selectivity Filter of the Voltage-gated Sodium Channel Is Involved in Channel Activation* , 2001, The Journal of Biological Chemistry.

[6]  M. Pinter,et al.  Sodium channel inactivation in an animal model of acute quadriplegic myopathy , 2001, Annals of neurology.

[7]  M. Rich,et al.  Altered Gene Expression in Steroid-Treated Denervated Muscle , 1999, Neurobiology of Disease.

[8]  R. Ruff Effects of temperature on slow and fast inactivation of rat skeletal muscle Na+channels. , 1999, American journal of physiology. Cell physiology.

[9]  H. Hartmann,et al.  Glycosylation Influences Voltage-Dependent Gating of Cardiac and Skeletal Muscle Sodium Channels , 1999, The Journal of Membrane Biology.

[10]  H. Fozzard,et al.  Ultra-slow inactivation in mu1 Na+ channels is produced by a structural rearrangement of the outer vestibule. , 1999, Biophysical journal.

[11]  P. Ruben,et al.  Slow inactivation in human cardiac sodium channels. , 1998, Biophysical journal.

[12]  R. Ruff,et al.  End‐plate voltage‐gated sodium channels are lost in clinical and experimental myasthenia gravis , 1998, Annals of neurology.

[13]  M. Pinter,et al.  Loss of electrical excitability in an animal model of acute quadriplegic myopathy , 1998, Annals of neurology.

[14]  M. Rich,et al.  Direct muscle stimulation in acute quadriplegic myopathy , 1997, Muscle & nerve.

[15]  S. Levinson,et al.  Contribution of Sialic Acid to the Voltage Dependence of Sodium Channel Gating , 1997, The Journal of general physiology.

[16]  P. Ruben,et al.  Interaction between fast and slow inactivation in Skm1 sodium channels. , 1996, Biophysical journal.

[17]  R. Ruff,et al.  Single-channel basis of slow inactivation of Na+ channels in rat skeletal muscle. , 1996, The American journal of physiology.

[18]  F. Sigworth,et al.  Impaired slow inactivation in mutant sodium channels. , 1996, Biophysical journal.

[19]  R. Ruff Sodium channel slow inactivation and the distribution of sodium channels on skeletal muscle fibres enable the performance properties of different skeletal muscle fibre types. , 1996, Acta physiologica Scandinavica.

[20]  M. Rich,et al.  Muscle is electrically inexcitable in acute quadriplegic myopathy , 1996, Neurology.

[21]  A. George,et al.  Comparison of heterologously expressed human cardiac and skeletal muscle sodium channels. , 1996, Biophysical journal.

[22]  S. Bendahhou,et al.  Serine-1321-independent regulation of the mu 1 adult skeletal muscle Na+ channel by protein kinase C. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[23]  R. Kallen,et al.  TTX-sensitive and TTX-insensitive sodium channel mRNA transcripts are independently regulated in adult skeletal muscle after denervation , 1991, Neuron.

[24]  W. Stühmer,et al.  Slow sodium channel inactivation in mammalian muscle: A possible role in regulating excitability , 1988, Muscle & nerve.

[25]  W. M. Roberts Sodium channels near end‐plates and nuclei of snake skeletal muscle. , 1987, The Journal of physiology.

[26]  W. Stühmer,et al.  Slow sodium channel inactivation in rat fast‐twitch muscle. , 1987, The Journal of physiology.

[27]  W. Stühmer,et al.  Comparison between slow sodium channel inactivation in rat slow‐ and fast‐twitch muscle. , 1987, The Journal of physiology.

[28]  W. Almers,et al.  Voltage clamp of rat and human skeletal muscle: measurements with an improved loose‐patch technique. , 1984, The Journal of physiology.

[29]  J. McArdle Molecular aspects of the trophic influence of nerve on muscle , 1983, Progress in Neurobiology.

[30]  H. Lorković,et al.  Potassium and chloride conductances in normal and denervated rat muscles. , 1977, The American journal of physiology.

[31]  D. Camerino,et al.  Effects of denervation and colchicine treatment on the chloride conductance of rat skeletal muscle fibers. , 1976, Journal of neurobiology.

[32]  R. Keynes The ionic channels in excitable membranes. , 1975, Ciba Foundation symposium.

[33]  D. K. Berg,et al.  Increased extrajunctional acetylcholine sensitivity produced by chronic acetylcholine sensitivity produced by chronic post‐synaptic neuromuscular blockade. , 1975, The Journal of physiology.

[34]  D. Noble,et al.  The kinetics and rectifier properties of the slow potassium current in cardiac Purkinje fibres , 1968, The Journal of physiology.

[35]  R B Stein,et al.  The threshold conditions for initiation of action potentials by excitable cells , 1966, The Journal of physiology.