Characteristics of a Transient Outward Current (sensitive to 4-aminopyridine) in Ca2+-tolerant Myocytes Isolated from the Rabbit Atrioventricular Node
Overview
Authors
Affiliations
A transient outward current (Ito) has been observed in the atrioventricular node (AVN), but its characteristics in Ca-tolerant AVN myocytes have not been investigated previously. In this study, Ito was measured from Ca-tolerant rabbit AVN myocytes at 37 degrees C, using the whole-cell patch-clamp technique. With interfering currents inhibited, 500-ms voltage-clamp pulses applied from -80 mV elicited Ito at potentials positive to -30 mV, which increased in magnitude with test potential amplitude. This current was completely blocked by external application of 5 mM 4-aminopyridine (4-AP). During a command pulse, Ito activated rapidly then inactivated with a bi-exponential time-course. Fast and slow time constants of current inactivation (tauf and taus, respectively) showed voltage dependence. At 0 mV, tauf was 14.5+/-2.7 ms and taus was 112.8+/-21. 2 ms, whilst at +60 mV tauf was 6.7+/-1.1 ms and taus was 63.7+/-9.2 ms (n=25). The steady-state inactivation relationship showed half-maximal inactivation at -33.8 mV (n=8). Re-activation of Ito after an inactivating pre-pulse showed a bi-exponential time-course of recovery: tau1 was 196+/-70 ms, and tau2 was 2707+/-1010 ms (n=6, at -80 mV). Repetitive application of voltage-clamp test pulses showed that Ito inactivation accumulated on repetitive stimulation, but reached a steady state rapidly for a given pulse frequency (0. 2-1.0 Hz). AVN Ito was sensitive to the class 1 anti-arrhythmic flecainide (EC50 for peak current of 24 microM), which showed selectivity for the rapidly inactivating current component. Quinidine also inhibited Ito in a dose-dependent fashion, but did not affect the current time-course. Under voltage-clamp conditions, a simulated diastolic depolarisation from -70 to -45 mV did not significantly reduce Ito amplitude, and under current-clamp conditions 4-AP inhibited spontaneous action potentials. Although this is consistent with a significant role for Ito in shaping AVN activity, under the conditions of this study 4-AP also partially blocked the "rapid" delayed rectifier current, IKr, and so the effects of 4-AP on action potentials could not be attributed exclusively to its effects on Ito.
George S, Faye N, Murillo-Berlioz A, Lee K, Trachiotis G, Efimov I Arrhythm Electrophysiol Rev. 2018; 6(4):179-185.
PMID: 29326832 PMC: 5739891. DOI: 10.15420/aer.2017.30.1.
Altered profile of mRNA expression in atrioventricular node of streptozotocin‑induced diabetic rats.
Howarth F, Parekh K, Jayaprakash P, Inbaraj E, Oz M, Dobrzynski H Mol Med Rep. 2017; 16(4):3720-3730.
PMID: 28731153 PMC: 5646948. DOI: 10.3892/mmr.2017.7038.
Cheng H, Cannell M, Hancox J Physiol Rep. 2017; 5(5).
PMID: 28270595 PMC: 5350179. DOI: 10.14814/phy2.13172.
Nikolaidou T, Cai X, Stephenson R, Yanni J, Lowe T, Atkinson A PLoS One. 2015; 10(10):e0141452.
PMID: 26509807 PMC: 4624927. DOI: 10.1371/journal.pone.0141452.
Transient outward potassium channel: a heart failure mediator.
He Q, Feng Y, Wang Y Heart Fail Rev. 2015; 20(3):349-62.
PMID: 25646587 DOI: 10.1007/s10741-015-9474-y.