TY - GEN
T1 - Spatially discordant alternans (SDAs) in intracellular calcium in paced quasi-1D cardiac tissue
AU - Jia, Z.
AU - Bien, H.
AU - Entcheva, E.
PY - 2007
Y1 - 2007
N2 - We characterize the development of calcium alternans in a long thin strip of cardiac tissue (cell monolayer). Our findings are compared to predictions of theoretical models about parameter profiles over space and nodal locations. We find that fine discordant regions emerge before macroscale propagation is visibly disturbed. SDA regions as small as 1-2 pixels are found and transitions between regions seem instantaneous in some cases, i.e. within the spatial resolution of the system (44mm). These fine SDA regions (fSDA) differ from our findings when synchronized large-scale SDA regions emerge (lSDA), where transition/nodal lines tend to be in the mm-range and the regions are at least a couple of millimeters in size. On the other hand, these results are in accord with theoretical predictions about the ability of intracellular calcium to alternate at a very fine scale. Our data show that fSDAs and lSDA differ in magnitude, spatial scale and level of spatial coherence; same samples can exhibit f SDA and lSDA at a higher pacing frequency. We discuss differences in the spatial distribution of major parameters of SDA between experiments and theory.
AB - We characterize the development of calcium alternans in a long thin strip of cardiac tissue (cell monolayer). Our findings are compared to predictions of theoretical models about parameter profiles over space and nodal locations. We find that fine discordant regions emerge before macroscale propagation is visibly disturbed. SDA regions as small as 1-2 pixels are found and transitions between regions seem instantaneous in some cases, i.e. within the spatial resolution of the system (44mm). These fine SDA regions (fSDA) differ from our findings when synchronized large-scale SDA regions emerge (lSDA), where transition/nodal lines tend to be in the mm-range and the regions are at least a couple of millimeters in size. On the other hand, these results are in accord with theoretical predictions about the ability of intracellular calcium to alternate at a very fine scale. Our data show that fSDAs and lSDA differ in magnitude, spatial scale and level of spatial coherence; same samples can exhibit f SDA and lSDA at a higher pacing frequency. We discuss differences in the spatial distribution of major parameters of SDA between experiments and theory.
UR - https://www.scopus.com/pages/publications/48749104322
U2 - 10.1109/NEBC.2007.4413399
DO - 10.1109/NEBC.2007.4413399
M3 - Conference contribution
AN - SCOPUS:48749104322
SN - 1424410339
SN - 9781424410330
T3 - Proceedings of the IEEE Annual Northeast Bioengineering Conference, NEBEC
SP - 307
EP - 308
BT - 33rd Annual Northeast Bioengineering Conference - Engineering Innovations in Life Sciences and Healthcare, NEBC
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 33rd Annual Northeast Bioengineering Conference, NEBC
Y2 - 10 March 2007 through 11 March 2007
ER -