Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis

S. C. Cannon, L. J. Hayward, J. Beech, R. H. Brown

Research output: Contribution to journalArticle

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Abstract

1. Equine hyperkalemic periodic paralysis (E-HPP) is a dominantly inherited disorder of muscle that causes recurrent episodes of stillness (myotonia) and weakness in association with elevated serum K+. Affected horses carry a mutant allele of the skeletal muscle isoform of the Na channel α-subunit. To understand how this mutation may cause the disease phenotype, the functional defect in Na channel behavior was defined physiologically by recording unitary currents from cell attached patches on normal and affected equine myotubes. 2. The presence of the mutation was confirmed in our cell line by restriction digest of polymerase chain reaction (PCR)-amplified genomic DNA. Myotubes from the affected horse were heterozygous for the point mutation that codes for a Phe to Leu substitution in S3 of domain IV. This assay provides a rapid technique to screen for the mutation in horses at risk. 3. The primary physiological defect in mutant Na channels was an impairment of inactivation. This defect was manifest as bursts of persistent activity during which the channel closed and reopened throughout a maintained depolarization. Disrupted inactivation slowed the decay of the ensemble- averaged current and produced an eightfold increase in the steady-state open probability measured at the end of a 40-ms pulse. This point mutation identifies a new region of the α subunit that is important for rapid inactivation of the channel. 4. The persistent Na current was produced by a distinct mode of gating. Failure of a mutant channel to inactivate was infrequent and occurred in groups of consecutive trials. Furthermore, the open time distributions for mutant Na channels contained a second, slow component (τ(s) = 1-2 ms) in addition to a fast component (τ(f) = 0.4 ms), which by itself was sufficient to represent the distribution in normal channels. These observations are consistent with the notion that channels slowly switch between two modes of inactivation: rapid versus noninactivating. Although the variance was high, for mutant channels there was a trend toward more frequent bursts of noninactivating behavior when extracellular K+ was increased. For Na channels in E-HPP myotubes, the ratio of steady-state to peak open probability increased threefold (0.024 from 0.008) in 10 versus 0 mM [K+](o). Conversely, in normal Na channels the steady-state to peak P(open) was 0.003 and invariant with [K+](o).

Original languageEnglish (US)
Pages (from-to)1892-1899
Number of pages8
JournalJournal of Neurophysiology
Volume73
Issue number5
StatePublished - 1995

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Hyperkalemic Periodic Paralysis
Sodium Channels
Horses
Skeletal Muscle Fibers
Point Mutation
Mutation
Myotonia
Normal Distribution
Muscular Diseases
Protein Isoforms
Skeletal Muscle
Alleles
Phenotype
Cell Line
Polymerase Chain Reaction
DNA
Serum

ASJC Scopus subject areas

  • Physiology
  • Neuroscience(all)

Cite this

Cannon, S. C., Hayward, L. J., Beech, J., & Brown, R. H. (1995). Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis. Journal of Neurophysiology, 73(5), 1892-1899.

Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis. / Cannon, S. C.; Hayward, L. J.; Beech, J.; Brown, R. H.

In: Journal of Neurophysiology, Vol. 73, No. 5, 1995, p. 1892-1899.

Research output: Contribution to journalArticle

Cannon, SC, Hayward, LJ, Beech, J & Brown, RH 1995, 'Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis', Journal of Neurophysiology, vol. 73, no. 5, pp. 1892-1899.
Cannon, S. C. ; Hayward, L. J. ; Beech, J. ; Brown, R. H. / Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis. In: Journal of Neurophysiology. 1995 ; Vol. 73, No. 5. pp. 1892-1899.
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