In a simulated 2-D tissue model, Na+ channel blockade decreased the vulnerable window of reentry, whereas K+ channel blockade increased it due to opposing effects on dynamical wave instability.
Does Na+ and K+ channel blockade affect vulnerability to and termination of fibrillation in simulated normal cardiac tissue?
Computational modeling demonstrates that Na+ and K+ channel blockade have opposing effects on the vulnerable window of reentry and dynamical wave instability during fibrillation.
Na(+) and K(+) channel-blocking drugs have anti- and proarrhythmic effects. Their effects during fibrillation, however, remain poorly understood. We used computer simulation of a two-dimensional (2-D) structurally normal tissue model with phase I of the Luo-Rudy action potential model to study the effects of Na(+) and K(+) channel blockade on vulnerability to and termination of reentry in simulated multiple-wavelet and mother rotor fibrillation. Our main findings are as follows: 1) Na(+) channel blockade decreased, whereas K(+) channel blockade increased, the vulnerable window of reentry in heterogeneous 2-D tissue because of opposing effects on dynamical wave instability. 2) Na(+) channel blockade increased the cycle length of reentry more than it increased refractoriness. In multiple-wavelet fibrillation, Na(+) channel blockade first increased and then decreased the average duration or transient time () of fibrillation. In mother rotor fibrillation, Na(+) channel blockade caused peripheral fibrillatory conduction block to resolve and the mother rotor to drift, leading to self-termination or sustained tachycardia. 3) K(+) channel blockade increased dynamical instability by steepening action potential duration restitution. In multiple-wavelet fibrillation, this effect shortened because of enhanced wave instability. In mother rotor fibrillation, this effect converted mother rotor fibrillation to multiple-wavelet fibrillation, which then could self-terminate. Our findings help illuminate, from a theoretical perspective, the possible underlying mechanisms of termination of different types of fibrillation by antiarrhythmic drugs.
Qu et al. (Sat,) conducted a other in Fibrillation. Na+ and K+ channel blockade was evaluated on Vulnerability to and termination of reentry in simulated multiple-wavelet and mother rotor fibrillation. In a simulated 2-D tissue model, Na+ channel blockade decreased the vulnerable window of reentry, whereas K+ channel blockade increased it due to opposing effects on dynamical wave instability.