Detailed Information on Publication Record
2017
A modified mathematical model of human ventricular cardiomyocyte incorporating separate t-tubular and surface dyads and submembrane spaces
PÁSEK, Michal, Markéta BÉBAROVÁ and Georges CHRISTÉBasic information
Original name
A modified mathematical model of human ventricular cardiomyocyte incorporating separate t-tubular and surface dyads and submembrane spaces
Authors
PÁSEK, Michal (203 Czech Republic), Markéta BÉBAROVÁ (203 Czech Republic, guarantor, belonging to the institution) and Georges CHRISTÉ (250 France)
Edition
Prague, Engineering Mechanics 2017, p. 750-753, 4 pp. 2017
Publisher
Academy of Sciences of the Czech Republic
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
20300 2.3 Mechanical engineering
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
Publication form
printed version "print"
References:
RIV identification code
RIV/00216224:14110/17:00095690
Organization unit
Faculty of Medicine
ISBN
978-80-214-5497-2
ISSN
UT WoS
000411657600177
Keywords in English
Human ventricular cell model; T-tubules; Dyads; Subsarcolemmal spaces; Calcium cycling
Tags
Tags
International impact, Reviewed
Změněno: 12/4/2018 10:34, Soňa Böhmová
Abstract
V originále
Intracellular Ca2+ load and Ca2+ transient are considerably dependent on distribution of sarcolemmal Ca2+ pump and Na+-Ca2+ exchanger between the t-tubular and surface membranes in the presence of separate dyadic and subsarcolemmal spaces in rat ventricular cell model. To explore analogical phenomenon in human, we modified our previously published model of human ventricular myocyte. When the t-tubular fractions of Na+-Ca2+ exchanger and of sarcolemmal Ca2+ pump were increased to the newly proposed value of 0.95 in the modified model, the following changes were observed at 1 Hz steady-state stimulation: a shortening of the action potential duration at 90 % repolarisation by 6 % and an increase of the cytosolic Ca2+ transient by 22 %. Further analysis revealed a critical role of Ca2+ concentration changes in the subsarcolemmal spaces and consequent change in cellular Ca2+ cycling in this effect.
Links
NV16-30571A, research and development project |
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