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Different Densities of Na-Ca Exchange Current in T-Tubular and Surface Membranes and Their Impact on Cellular Activity in a Model of Rat Ventricular Cardiomyocyte

The ratio of densities of Na-Ca exchanger current (I(NaCa)) in the t-tubular and surface membranes (I(NaCa)-ratio) computed from the values of I(NaCa) and membrane capacitances (C(m)) measured in adult rat ventricular cardiomyocytes before and after detubulation ranges between 1.7 and 25 (potentiall...

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Detalles Bibliográficos
Autores principales: Pásek, M., Šimurda, J., Christé, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340987/
https://www.ncbi.nlm.nih.gov/pubmed/28321411
http://dx.doi.org/10.1155/2017/6343821
Descripción
Sumario:The ratio of densities of Na-Ca exchanger current (I(NaCa)) in the t-tubular and surface membranes (I(NaCa)-ratio) computed from the values of I(NaCa) and membrane capacitances (C(m)) measured in adult rat ventricular cardiomyocytes before and after detubulation ranges between 1.7 and 25 (potentially even 40). Variations of action potential waveform and of calcium turnover within this span of the I(NaCa)-ratio were simulated employing previously developed model of rat ventricular cell incorporating separate description of ion transport systems in the t-tubular and surface membranes. The increase of I(NaCa)-ratio from 1.7 to 25 caused a prolongation of APD (duration of action potential at 90% repolarisation) by 12, 9, and 6% and an increase of peak intracellular Ca(2+) transient by 45, 19, and 6% at 0.1, 1, and 5 Hz, respectively. The prolonged APD resulted from the increase of I(NaCa) due to the exposure of a larger fraction of Na-Ca exchangers to higher Ca(2+) transients under the t-tubular membrane. The accompanying rise of Ca(2+) transient was a consequence of a higher Ca(2+) load in sarcoplasmic reticulum induced by the increased Ca(2+) cycling between the surface and t-tubular membranes. However, the reason for large differences in the I(NaCa)-ratio assessed from measurements in adult rat cardiomyocytes remains to be explained.