Journal of human genetics · 2009
Role of HCN4 channel in preventing ventricular arrhythmia.
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Ueda Kazuo, Hirano Yuji, Higashiuesato Yasushi, Aizawa Yoshiyasu, Hayashi Takeharu, Inagaki Natsuko, Tana Takeshi, Ohya Yusuke, Takishita Shuichi, Muratani Hiromi, Hiraoka Masayasu, Kimura Akinori
Аннотация
Bradycardia is a trigger of ventricular arrhythmias in patients with arrhythmia including Brugada syndrome and long QT syndrome. The HCN4 channel controls the heart rate, and its mutations predispose to inherited sick sinus syndrome and long QT syndrome associated with bradycardia. We found a 4 base-insertion at the splice donor site of the HCN4 gene in a patient with idiopathic ventricular tachycardia, which was supposed to generate a truncated channel. To investigate the role of the HCN4 channel in ventricular arrhythmia, we introduced a ventricular action potential of I(f) channel produced by HCN4 in a computer simulation model and found that the I(f) channel generated a leaky outward current during the plateau phase of ventricular action potential. Currents through the I(f) channel were suggested to contribute to the shortening of the action potential duration and the prevention of early after-depolarization in bradycardia. These observations suggested that the HCN4 channel played a preventive role in triggering bradycardia-induced ventricular arrhythmias.
Предметные рубрики MeSH
Action PotentialsArrhythmias, CardiacBase SequenceComputer SimulationCyclic Nucleotide-Gated Cation ChannelsHeart VentriclesHumansHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsIon Channel GatingModels, BiologicalMolecular Sequence DataMuscle ProteinsMutationPotassium ChannelsRNA Splicing