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Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease
- Source :
- American Journal of Physiology-Heart and Circulatory Physiology. 292:H399-H407
- Publication Year :
- 2007
- Publisher :
- American Physiological Society, 2007.
-
Abstract
- Some mutations of the sodium channel gene NaV1.5 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 ΔK1479 shifts the potential of half-activation, V1/2m, to more positive potentials ( V1/2m = −36.8 ± 0.8 and −24.5 ± 1.3 mV for the wild-type and ΔK1479 mutant respectively, n = 11, 10). The depolarizing shift increases the extent of depolarization required for activation. The potential of half-inactivation, V1/2h, is also shifted to more positive potentials ( V1/2h = −85 ± 1.1 and −79.4 ± 1.2 mV for wild-type and ΔK1479 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.
- Subjects :
- medicine.medical_specialty
Pre-Excitation Syndromes
Heart disease
Physiology
Sodium
Action Potentials
Muscle Proteins
chemistry.chemical_element
NAV1.5 Voltage-Gated Sodium Channel
Kidney
medicine.disease_cause
Sodium Channels
Cell Line
Structure-Activity Relationship
Heart Conduction System
Physiology (medical)
Internal medicine
medicine
Humans
Computer Simulation
Brugada Syndrome
Brugada syndrome
Mutation
business.industry
Sodium channel
Models, Cardiovascular
medicine.disease
Kinetics
Endocrinology
chemistry
Circulatory system
Electrical conduction system of the heart
Cardiology and Cardiovascular Medicine
business
Ion Channel Gating
Subjects
Details
- ISSN :
- 15221539 and 03636135
- Volume :
- 292
- Database :
- OpenAIRE
- Journal :
- American Journal of Physiology-Heart and Circulatory Physiology
- Accession number :
- edsair.doi.dedup.....17194d8413a09c8ac666ace9f2e0585e