PÁSEK, Michal a Jiří ŠIMURDA. Quantitative modelling of interaction of propafenone with sodium channels in cardiac cells. In Proceedings of the International Federation for Medical and Biologocal Engineering. Pula (Croatia): Faculty of Electrical Engineering, Zagreb, 2001, s. 1028-1031. ISBN 953-184-024-5.
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Základní údaje
Originální název Quantitative modelling of interaction of propafenone with sodium channels in cardiac cells.
Autoři PÁSEK, Michal (203 Česká republika, garant) a Jiří ŠIMURDA (203 Česká republika).
Vydání Pula (Croatia), Proceedings of the International Federation for Medical and Biologocal Engineering, s. 1028-1031, 2001.
Nakladatel Faculty of Electrical Engineering, Zagreb
Další údaje
Originální jazyk angličtina
Typ výsledku Stať ve sborníku
Obor 10610 Biophysics
Stát vydavatele Chorvatsko
Utajení není předmětem státního či obchodního tajemství
Kód RIV RIV/00216224:14110/01:00005060
Organizační jednotka Lékařská fakulta
ISBN 953-184-024-5
UT WoS 000176065600281
Klíčová slova anglicky cardiac cell; propafenone; quantitative modelling
Štítky Cardiac cell, propafenone, Quantitative modelling
Změnil Změnil: doc. Ing. Michal Pásek, Ph.D., učo 46541. Změněno: 25. 6. 2009 16:20.
Anotace
A mathematical model of the interaction of propafenone with sodium channels is based on experimental data that demonstrate use dependent effect of the drug. Transitions among channel states are described by a kinetic diagram and a corre-sponding set of differential equations. The values of rate constants of the drug-receptor reaction are fitted to experimental data by repeated computer simulations using a genetic algorithm. The model suggests the following interpretation of the obtained experimental results: 1) The affinity of the drug to its binding site is high in the open and inactivated states while it is low in the resting state. 2) The biphasic development of the block during depolarization is consistent with a high association rate constant in the open state and a lower one in the inactivated state. 3) The observed double exponential time course of recovery of INa at resting voltage after depolarizing pulse may result from concurrent drug release from inactivated and non-inactivated blocked channels.
VytisknoutZobrazeno: 14. 5. 2024 21:20