Insights into the molecular mechanisms of bradycardia-triggered arrhythmias in long QT-3 syndrome

Colleen E Clancy, Michihiro Tateyama, Robert S. Kass

Research output: Contribution to journalArticlepeer-review

73 Scopus citations


Congenital long QT syndrome is a rare disease in which the electrocardiogram QT interval is prolonged due to dysfunctional ventricular repolarization. Variant 3 (LQT-3) is associated with mutations in SCN5A, the gene coding for the heart Na+ channel α subunit. Arrhythmias in LQT-3 mutation carriers are more likely to occur at rest, when heart rate is slow. Several LQT-3 Na+ channel mutations exert their deleterious effects by promoting a mode of Na+ channel gating wherein a fraction of channels fails to inactivate. This gating mode, termed "bursting," results in sustained macroscopic inward Na+ channel current (Isus), which can delay repolarization and prolong the QT interval. However, the mechanism of heart-rate dependence of Isus has been unresolved at the single-channel level. We investigate an LQT-3 mutant (Y1795C) using experimental and theoretical frameworks to elucidate the molecular mechanism of Isus rate dependence. Our results indicate that mutation-induced changes in the length of time mutant channels spend bursting, rather than how readily they burst, determines Isus inverse heart-rate dependence. These results link mutation-induced changes in Na+ channel gating mode transitions to heart rate-dependent changes in cellular electrical activity underlying a key LQT-3 clinical phenotype.

Original languageEnglish (US)
Pages (from-to)1251-1262
Number of pages12
JournalJournal of Clinical Investigation
Issue number9
StatePublished - Nov 2002
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)


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