Why the study?
What are the mechanisms underlying action potential duration rate adaptation in human atrial cells, and does delayed adaptation increase proarrhythmic risk?
What are the mechanisms underlying action potential duration rate adaptation in human atrial cells, and does delayed adaptation increase proarrhythmic risk?
Computational modeling reveals that human atrial action potential duration adaptation to heart rate changes is a biphasic process taking over 8 minutes, and delays in this adaptation are linked to increased proarrhythmic risk.
Abnormal adaptation of action potential duration (APD) to changes in heart rate (HR) has been suggested as an indicator of increased arrhythmic risk. In this study, we investigate the mechanisms underlying APD rate adaptation in human atrial cells and its relationship to arrhythmogenesis. Simulations are performed using action potential computational models and results are compared with experimental data from the literature. APD rate adaptation in response to sudden sustained HR changes is shown to take more than 8 minutes to be completed in the simulations and two main adaptation phases can be identified: a fast initial one due to the Na+/Ca2+ exchanger and the L-type calcium current; and a subsequent slow accommodation determined by intracellular Na dynamics. Both APD adaptation dynamics and its underlying mechanisms are found to be consistent in different species. Alterations in ionic mechanisms leading to delayed APD adaptation are associated with increased proarrhythmic risk. 1.
No takes yet. Share an insight, caveat, or question.
Sánchez et al. (2009) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: