TY - JOUR
T1 - Simulation of developmental changes in action potentials with ventricular cell models
AU - Itoh, Hitomi
AU - Naito, Yasuhiro
AU - Tomita, Masaru
N1 - Funding Information:
Acknowledgements This work was supported in part by a grant-in-aid from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (the Leading Project for Biosimulation and the 21st Century Center of Excellence [COE] Program: Understanding and Control of Life’s Function via Systems Biology).
PY - 2007/3
Y1 - 2007/3
N2 - During cardiomyocyte development, early embryonic ventricular cells show spontaneous activity that disappears at a later stage. Dramatic changes in action potential are mediated by developmental changes in individual ionic currents. Hence, reconstruction of the individual ionic currents into an integrated mathematical model would lead to a better understanding of cardiomyocyte development. To simulate the action potential of the rodent ventricular cell at three representative developmental stages, quantitative changes in the ionic currents, pumps, exchangers, and sarcoplasmic reticulum (SR) Ca2+ kinetics were represented as relative activities, which were multiplied by conductance or conversion factors for individual ionic systems. The simulated action potential of the early embryonic ventricular cell model exhibited spontaneous activity, which ceased in the simulated action potential of the late embryonic and neonatal ventricular cell models. The simulations with our models were able to reproduce action potentials that were consistent with the reported characteristics of the cells in vitro. The action potential of rodent ventricular cells at different developmental stages can be reproduced with common sets of mathematical equations by multiplying conductance or conversion factors for ionic currents, pumps, exchangers, and SR Ca 2+ kinetics by relative activities.
AB - During cardiomyocyte development, early embryonic ventricular cells show spontaneous activity that disappears at a later stage. Dramatic changes in action potential are mediated by developmental changes in individual ionic currents. Hence, reconstruction of the individual ionic currents into an integrated mathematical model would lead to a better understanding of cardiomyocyte development. To simulate the action potential of the rodent ventricular cell at three representative developmental stages, quantitative changes in the ionic currents, pumps, exchangers, and sarcoplasmic reticulum (SR) Ca2+ kinetics were represented as relative activities, which were multiplied by conductance or conversion factors for individual ionic systems. The simulated action potential of the early embryonic ventricular cell model exhibited spontaneous activity, which ceased in the simulated action potential of the late embryonic and neonatal ventricular cell models. The simulations with our models were able to reproduce action potentials that were consistent with the reported characteristics of the cells in vitro. The action potential of rodent ventricular cells at different developmental stages can be reproduced with common sets of mathematical equations by multiplying conductance or conversion factors for ionic currents, pumps, exchangers, and SR Ca 2+ kinetics by relative activities.
KW - Cardiac ventricular cell
KW - Computer modeling
KW - Development
KW - Electrophysiology
KW - Ion channels
KW - Spontaneous electrical activity
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U2 - 10.1007/s11693-006-9002-4
DO - 10.1007/s11693-006-9002-4
M3 - Article
C2 - 19003434
AN - SCOPUS:34547381688
SN - 1872-5325
VL - 1
SP - 11
EP - 23
JO - Systems and Synthetic Biology
JF - Systems and Synthetic Biology
IS - 1
ER -