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Inhibition of Small-Conductance Ca(2+)-Activated K(+) Channels Terminates and Protects Against Atrial Fibrillation RID G-4860-2011

Author:
Diness, Jonas Goldin  Sorensen, Ulrik S.  Nissen, Jakob Dahl  Al-Shahib, Baha  Jespersen, Thomas  Grunnet, Morten  Hansen, Rie Schultz  


Journal:
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY


Issue Date:
2010


Abstract(summary):

Background-Recently, evidence has emerged that small-conductance Ca(2+)-activated K(+) (SK) channels are predominantly expressed in the atria in a number of species including human. In rat, guinea pig, and rabbit ex vivo and in vivo models of atrial fibrillation (AF), we used 3 different SK channel inhibitors, UCL1684, N-(pyridin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine (ICA), and NS8593, to assess the hypothesis that pharmacological inhibition of SK channels is antiarrhythmic. Methods and Results-In isolated, perfused guinea pig hearts, AF could be induced in all control hearts (n=7) with a combination of 1 mu mol/L acetylcholine combined with electric stimulation. Pretreatment with 3 mu mol/L NS8593, which had no effect on QT interval, prolonged the atrial effective refractory period by 37.1 +/- 7.7% (P<0.001) and prevented acetylcholine-induced AF (P<0.001, n=7). After AF induction, perfusion with NS8593 (10 mu mol/L), UCL1684 (1 mu mol/L), or ICA (1 mu mol/L) terminated AF in all hearts, comparable to 10 mu mol/L amiodarone. In isolated, perfused rat hearts, AF was induced with electric stimulation; 10 mu mol/L NS8593 terminated AF and prevented reinduction of AF in all hearts (n=6, P<0.001). In all hearts, AF could be reinduced after washing. In isolated, perfused rabbit hearts, AF was induced with 10 mu mol/L acetylcholine and burst pacing; 10 mu mol/L NS8593 terminated AF and prevented reinduction of AF in all hearts (n=6, P<0.001). After washing, AF could be reinduced in 75% of the hearts (n=4, P=0.06). In an in vivo rat model of acute AF induced by burst pacing, injection of 5 mg/kg of either NS8593 or amiodarone shortened AF duration significantly to (23.2 +/- 20.0%, P<0.001, n=5, and 26.2 +/- 17.9%, P<0.001, n=5, respectively) as compared with injection of vehicle (96.3 +/- 33.2%, n=5). Conclusions-Inhibition of SK channels prolongs atrial effective refractory period without affecting QT interval and prevents and terminates AF ex vivo and in vivo, thus offering a promising new therapeutic opportunity in the treatment of AF. (Circ Arrhythm Electrophysiol. 2010;3:380-390.)


Page:
380---U121


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