Referenced in: HCN3

Automatically associated channels: HCN3 , HCN4 , Slo1

Title: HCN3 contributes to the ventricular action potential waveform in the murine heart.

Authors: Stefanie Fenske, Robert Mader, Andreas Scharr, Christos Paparizos, Xiaochun Cao-Ehlker, Stylianos Michalakis, Lior Shaltiel, Martha Weidinger, Juliane Stieber, Susanne Feil, Robert Feil, Franz Hofmann, Christian Wahl-Schott, Martin Biel

Journal, date & volume: Circ. Res., 2011 Oct 14 , 109, 1015-23

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21903939

Abstract
The hyperpolarization-activated current I(h) that is generated by hyperpolarization-activated cyclic nucleotide-gated channels (HCNs) plays a key role in the control of pacemaker activity in sinoatrial node cells of the heart. By contrast, it is unclear whether I(h) is also relevant for normal function of cardiac ventricles.To study the role of the HCN3-mediated component of ventricular I(h) in normal ventricular function.To test the hypothesis that HCN3 regulates the ventricular action potential waveform, we have generated and analyzed a HCN3-deficient mouse line. At basal heart rate, mice deficient for HCN3 displayed a profound increase in the T-wave amplitude in telemetric electrocardiographic measurements. Action potential recordings on isolated ventricular myocytes indicate that this effect was caused by an acceleration of the late repolarization phase in epicardial myocytes. Furthermore, the resting membrane potential was shifted to more hyperpolarized potentials in HCN3-deficient mice. Cardiomyocytes of HCN3-deficient mice displayed approximately 30% reduction of total I(h). At physiological ionic conditions, the HCN3-mediated current had a reversal potential of approximately -35 mV and displayed ultraslow deactivation kinetics.We propose that HCN3 together with other members of the HCN channel family confer a depolarizing background current that regulates ventricular resting potential and counteracts the action of hyperpolarizing potassium currents in late repolarization. In conclusion, our data indicate that HCN3 plays an important role in shaping the cardiac action potential waveform.