Single_stim_experiment.cellml
Single stimulation experiment
In the Single stimulation experiment, the Excitation-contraction component is configured and parameterised with an applied Single pulse patch clamp protocol.
You can change the parameters of stimulation in the component Vstim_para.
You can also bypass the parameters in the component model_parameters and initial_conditions and define your own parameters. We defined control_para to alter some parameters such as intracellular Na + concentration for specific experiments.
The simulation experiment can be obtained by loading the corresponding SED-ML document into OpenCOR and executing the simulation.
Control of Intracellular Ca2 + Concentration
The experiment setting to reproduce Figure 2-4 is summarized in the following:
Figure [1] shows simulations of Ca2 + i decay (in nM). A: Ca2 + i decay under inhibition of Ca2 + pumps. B: Ca2 + i decay in control conditions.
[1] |
Figure [2] shows simulations of Ca2 + i rise and decay following a 200 ms voltage pulse from a holding potential of -50 mV to pulse potentials of 0 mV (A), 10 mV (B), and -10 mV (C).
[2] |
Figure [3] shows simulations of Ca2 + i rise and decay following a 200 ms voltage pulse from a holding potential of -50 mV to pulse potentials of -20 mV (A) and 20 mV (B).
[3] |
The experiment setting to reproduce primary Figure 5A and 5B are the same as the one used in primary Figure 2B and Figure 3A, respectively.
Figure [4] shows simulations of Ca2 + fluxes through various Ca2 + control mechanisms. Plot A shows Ca2 + flux through Na + ⁄ Ca2 + exchangers and Ca2 + pumps during Ca2 + i decay for a holding potential of -80 mV followed by a 750 ms voltage pulse to 0 mV, while plot B shows Ca2 + flux through Ca2 + channels and Ca2 + extraction mechanisms during Ca2 + rise and decay in response to a 200 ms voltage pulse to 0 mV from a holding potential of -50 mV.
[4] |