Key result
Reduced IK1 or IKr partially explains age-related APD prolongation in computational models.
Why the study?
Age-related changes in the electrical function of human atrial cardiomyocytes that may trigger atrial fibrillation are poorly understood.
Age-related prolongation of the action potential in atrial cardiomyocytes may require a combined inhibition of I_K1 and I_Kr to fully explain observed physiological changes.
The risk of developing atrial fibrillation increases with age. However, the age-related changes in the electrical function of human atrial cardiomyocytes that may trigger atrial fibrillation are poorly understood. This study examined two possible scenarios of age-related modulation of potassium currents, either <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IK1</tex> or <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IKr</tex>, and their effects on action potential duration (APD). For both scenarios, based on the physiological data, three ageing groups of ionic cell models were created depending on the severity of age-dependent changes in the particular ionic currents: Adult, Senior I, and Senior II. For each of the two considered aging scenarios we were able to reproduce most of aging dependent features of intracellular calcium dynamics and action potentials. However, both hypotheses have their advantages and disadvantages. In the scenario with <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IKr</tex> change, the resting membrane potential was age independent, which is consistent with the experimental data. Meanwhile, APDs in all age groups in this scenario were close to the lower limit of the acceptable physiologic range. In contrast, in the scenario with <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IK1</tex> change, resting potential varied with age, but APDs were closer to the mean values of the physiologic range. Thus, the age-related prolongation of the action potential could be explained by either age-related reduction in <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IK1</tex> or in <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IKr</tex>, but neither scenario fully explains the age-related changes. Perhaps a combined age-related inhibition of <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IK1</tex> and <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">IKr</tex> could resolve these discrepancies.
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Belogurova et al. (2024) studied Atrial fibrillation. Age-related modulation of potassium currents (IK1 or IKr) vs. Adult models was evaluated on Action potential duration (APD) and resting membrane potential. Age-related prolongation of the action potential in computational models could be explained by reduction in IK1 or IKr, though neither scenario fully explains all age-related changes.
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