2014
Effect of Ca2+ Efflux Pathway Distribution and Exogenous Ca2+ Buffers on Intracellular Ca2+ Dynamics in the Rat Ventricular Myocyte: A Simulation Study
PÁSEK, Michal; Jiří ŠIMURDA a Clive H. ORCHARDZákladní údaje
Originální název
Effect of Ca2+ Efflux Pathway Distribution and Exogenous Ca2+ Buffers on Intracellular Ca2+ Dynamics in the Rat Ventricular Myocyte: A Simulation Study
Autoři
PÁSEK, Michal; Jiří ŠIMURDA a Clive H. ORCHARD
Vydání
BioMed Research International, New York, Hindawi Publishing Corporation, 2014, 2314-6133
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30105 Physiology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.579
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/14:00080146
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
SARCOPLASMIC-RETICULUM; T-TUBULES; CARDIAC MYOCYTES; SURFACE-MEMBRANE; CALCIUM-RELEASE; INACTIVATION; EXCHANGE; CHANNELS; MUSCLE
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 14. 10. 2014 15:49, Soňa Böhmová
Anotace
V originále
We have used a previously published computer model of the rat cardiac ventricular myocyte to investigate the effect of changing the distribution of Ca2+ efflux pathways (SERCA, Na+/Ca2+ exchange, and sarcolemmal Ca2+ ATPase) between the dyad and bulk cytoplasm and the effect of adding exogenous Ca2+ buffers (BAPTA or EGTA), which are used experimentally to differentially buffer Ca2+ in the dyad and bulk cytoplasm, on cellular Ca2+ cycling. Increasing the dyadic fraction of a particular Ca2+ efflux pathway increases the amount of Ca2+ removed by that pathway, with corresponding changes in Ca2+ efflux from the bulk cytoplasm. The magnitude of these effects varies with the proportion of the total Ca2+ removed from the cytoplasm by that pathway. Differences in the response to EGTA and BAPTA, including changes in Ca2+-dependent inactivation of the L-type Ca2+ current, resulted from the buffers acting as slow and fast "shuttles," respectively, removing Ca2+ from the dyadic space. The data suggest that complex changes in dyadic Ca2+ and cellular Ca2+ cycling occur as a result of changes in the location of Ca2+ removal pathways or the presence of exogenous Ca2+ buffers, although changing the distribution of Ca2+ efflux pathways has relatively small effects on the systolic Ca2+ transient.
Návaznosti
| NT14301, projekt VaV |
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