@article {morotti2018effects,
	title = {Effects of modulation of small-conductance calcium-activated potassium current on atrial electrophysiology and arrhythmogenesis: a population-based computational study},
	journal = {Biophysical Journal},
	volume = {114},
	number = {3},
	year = {2018},
	pages = {473a},
	publisher = {{Elsevier},
	author = {Morotti, Stefano and Ellinwood, Nicholas and Ni, Haibo and Jussi T {Koivum{\"a}ki} and Maleckar, Molly and Heijman, Jordi and Dobrev, Dobromir and Grandi, Eleonora}
}
@misc {26368,
	title = {A Novel Computational Model of the Rabbit Atrial Myocyte Offers Insight into Calcium Wave Propagation Failure},
	howpublished = {Biophysical Journal},
	year = {2018},
	month = {Jan-02-2018},
	address = {Cambridge, USA},
	abstract = {Atrial cardiomyocytes have a less well-developed T-tubule system than ventricular cells, resulting in intracellular calcium waves propagating from the membrane to the center via centripetal calcium diffusion. Failure of centripetal calcium-wave propagation ({\textquoteleft}calcium silencing{\textquoteright}) has been observed in a rabbit model of rapid atrial pacing and in patients with atrial fibrillation, but the underlying mechanisms remain incompletely understood. The goal of this study was to develop a novel computational model of the rabbit atrial cardiomyocyte that incorporates detailed compartmentalization of intracellular calcium dynamics, which can be used to investigate the mechanisms underpinning calcium silencing.
We incorporated ion-current formulations reflecting rabbit electrophysiology into a previously published human atrial cardiomyocyte model. The model was validated with published experimental data and the effects of altered rate of calcium diffusion between the calcium-release-unit space and the cytosol (τdiff) were investigated. τdiff modulates local calcium levels available to activate neighboring calcium-release sites, affecting wave propagation.
Simulation results showed that calcium-wave propagation was highly sensitive to τdiff during normal pacing at 2 Hz. We observed impaired calcium-wave propagation for a range of values of τdiff, with full calcium-wave propagation for values of τdiff exceeding 12.7 ms, and calcium silencing for values of τdiff below 10.6 ms due to insufficient local positive feedback for calcium-induced calcium release to maintain centripetal wave propagation. We also observed calcium alternans between propagating and non-propagating waves for intermediate values of τdiff.
This study provided new insight into the mechanisms of calcium-wave propagation failure in rabbit atrial cardiomyocytes and motivates further investigation of the effects of altered calcium diffusion on wave-propagation abnormalities and calcium-dependent arrhythmogenesis. Moreover, the newly developed model will be a useful tool for studying conditions which permit restoration of normal calcium wave propagation.},
	issn = {00063495},
	doi = {10.1016/j.bpj.2017.11.680},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0006349517319124https://api.elsevier.com/content/article/PII:S0006349517319124?httpAccept=text/xmlhttps://api.elsevier.com/content/article/PII:S0006349517319124?httpAccept=text/plain},
	author = {Vagos, Marcia and Heijman, Jordi and Arevalo, Hermenegild and Maleckar, Molly and Bernardo Lino {de Oliveira} and Schotten, Ulrich and Sundnes, Joakim}
}
@article {vagos2018novel,
	title = {A Novel Computational Model of the Rabbit Atrial Myocyte Offers Insight into Calcium Wave Propagation Failure},
	journal = {Biophysical Journal},
	volume = {114},
	number = {3},
	year = {2018},
	pages = {119a},
	publisher = {{Elsevier},
	author = {M{\'a}rcia R {Vagos} and Heijman, Jordi and Arevalo, Hermenegild and Maleckar, Molly and Bernardo Lino {de Oliveira} and Schotten, Ulrich and Sundnes, Joakim}
}
