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Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease.

Publication ,  Journal Article
Zhang, Z-S; Tranquillo, J; Neplioueva, V; Bursac, N; Grant, AO
Published in: Am J Physiol Heart Circ Physiol
January 2007

Some mutations of the sodium channel gene Na(V1.5) are multifunctional, causing combinations of LQTS, Brugada syndrome and progressive cardiac conduction system disease (PCCD). The combination of Brugada syndrome and PCCD is uncommon, although they both result from a reduction in the sodium current. We hypothesize that slow conduction is sufficient to cause S-T segment elevation and undertook a combined experimental and theoretical study to determine whether conduction slowing alone can produce the Brugada phenotype. Deletion of lysine 1479 in one of two positively charged clusters in the III/IV inter-domain linker causes both syndromes. We have examined the functional effects of this mutation using heterologous expression of the wild-type and mutant sodium channel in HEK-293-EBNA cells. We show that DeltaK1479 shifts the potential of half-activation, V(1/2m), to more positive potentials (V(1/2m) = -36.8 +/- 0.8 and -24.5 +/- 1.3 mV for the wild-type and DeltaK1479 mutant respectively, n = 11, 10). The depolarizing shift increases the extent of depolarization required for activation. The potential of half-inactivation, V(1/2h), is also shifted to more positive potentials (V(1/2h) = -85 +/- 1.1 and -79.4 +/- 1.2 mV for wild-type and DeltaK1479 mutant respectively), increasing the fraction of channels available for activation. These shifts are quantitatively the same as a mutation that produces PCCD only, G514C. We incorporated experimentally derived parameters into a model of the cardiac action potential and its propagation in a one dimensional cable (simulating endo-, mid-myocardial and epicardial regions). The simulations show that action potential and ECG changes consistent with Brugada syndrome may result from conduction slowing alone; marked repolarization heterogeneity is not required. The findings also suggest how Brugada syndrome and PCCD which both result from loss of sodium channel function are sometimes present alone and at other times in combination.

Duke Scholars

Published In

Am J Physiol Heart Circ Physiol

DOI

ISSN

0363-6135

Publication Date

January 2007

Volume

292

Issue

1

Start / End Page

H399 / H407

Location

United States

Related Subject Headings

  • Structure-Activity Relationship
  • Sodium Channels
  • Pre-Excitation Syndromes
  • NAV1.5 Voltage-Gated Sodium Channel
  • Mutation
  • Muscle Proteins
  • Models, Cardiovascular
  • Kinetics
  • Kidney
  • Ion Channel Gating
 

Citation

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MLA
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Zhang, Z.-S., Tranquillo, J., Neplioueva, V., Bursac, N., & Grant, A. O. (2007). Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease. Am J Physiol Heart Circ Physiol, 292(1), H399–H407. https://doi.org/10.1152/ajpheart.01025.2005
Zhang, Zhu-Shan, Joseph Tranquillo, Valentina Neplioueva, Nenad Bursac, and Augustus O. Grant. “Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease.Am J Physiol Heart Circ Physiol 292, no. 1 (January 2007): H399–407. https://doi.org/10.1152/ajpheart.01025.2005.
Zhang Z-S, Tranquillo J, Neplioueva V, Bursac N, Grant AO. Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease. Am J Physiol Heart Circ Physiol. 2007 Jan;292(1):H399–407.
Zhang, Zhu-Shan, et al. “Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease.Am J Physiol Heart Circ Physiol, vol. 292, no. 1, Jan. 2007, pp. H399–407. Pubmed, doi:10.1152/ajpheart.01025.2005.
Zhang Z-S, Tranquillo J, Neplioueva V, Bursac N, Grant AO. Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease. Am J Physiol Heart Circ Physiol. 2007 Jan;292(1):H399–H407.

Published In

Am J Physiol Heart Circ Physiol

DOI

ISSN

0363-6135

Publication Date

January 2007

Volume

292

Issue

1

Start / End Page

H399 / H407

Location

United States

Related Subject Headings

  • Structure-Activity Relationship
  • Sodium Channels
  • Pre-Excitation Syndromes
  • NAV1.5 Voltage-Gated Sodium Channel
  • Mutation
  • Muscle Proteins
  • Models, Cardiovascular
  • Kinetics
  • Kidney
  • Ion Channel Gating