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Publication : Action potential wavelength restitution predicts alternans and arrhythmia in murine Scn5a(+/-) hearts.

First Author  Matthews GD Year  2013
Journal  J Physiol Volume  591
Issue  17 Pages  4167-88
PubMed ID  23836691 Mgi Jnum  J:214178
Mgi Id  MGI:5588530 Doi  10.1113/jphysiol.2013.254938
Citation  Matthews GD, et al. (2013) Action potential wavelength restitution predicts alternans and arrhythmia in murine Scn5a(+/-) hearts. J Physiol 591(Pt 17):4167-88
abstractText  Reductions in cardiac action potential wavelength, and the consequent wavebreak, have been implicated in arrhythmogenesis. Tachyarrhythmias are more common in the Brugada syndrome, particularly following pharmacological challenge, previously modelled using Scn5a(+/-) murine hearts. Propagation latencies and action potential durations (APDs) from monophasic action potential recordings were used to assess wavelength changes with heart rate in Langendorff-perfused wild-type (WT) and Scn5a(+/-) hearts. Recordings were obtained from right (RV) and left (LV) ventricular, epicardial and endocardial surfaces during incremental pacing, before and following flecainide or quinidine challenge. Conduction velocities (theta'), action potential wavelengths (lambda' = APD x theta'), and their corresponding alternans depended non-linearly upon diastolic interval (DI). Maximum theta' was lower in Scn5a(+/-) RV epicardium than endocardium. Flecainide further reduced theta', accentuating this RV conduction block. Quinidine reduced maximum theta' in WT and caused earlier conduction failure in the RV of both Scn5a(+/-) and WT. Use of recovery wavelengths (lambda'0 = DI x theta') rather than DI, provided novel lambda restitution plots of lambda' against lambda'0, which sum to a basic cycle distance permitting feedback analysis. lambda' restitution gradient better correlated with alternans magnitude than either APD or theta restitution gradient. The large differences in theta' and APD restitution contrasted with minor differences in maximum lambda' between epi- and endocardia of untreated hearts, and quinidine-treated WT hearts. Strikingly, all regions and conditions converged to a common instability point, implying a conserved relationship. Flecainide or quinidine decreased the pacing rates at which this occurred, through reducing basic cycle distance, in the Scn5a(+/-) RV epicardium, directly predictive of its arrhythmic phenotype.
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