%0 Journal Article %1 Aust_2006_334 %A Austin, Travis M %A Hooks, Darren A %A Hunter, Peter J %A Nickerson, David P %A Pullan, Andrew J %A Sands, Gregory B %A Smaill, Bruce H %A Trew, Mark L %D 2006 %J Ann. N. Y. Acad. Sci. %K Biological Heart; Humans; Models, %P 334--347 %R 10.1196/annals.1380.025 %T Modeling cardiac electrical activity at the cell and tissue levels. %U http://dx.doi.org/10.1196/annals.1380.025 %V 1080 %X Significant tissue structures exist in cardiac ventricular tissue, which are of supracellular dimension. It is hypothesized that these tissue structures contribute to the discontinuous spread of electrical activation, may contribute to arrhythmogenesis, and also provide a substrate for effective cardioversion. However, the influences of these mesoscale tissue structures in intact ventricular tissue are difficult to understand solely on the basis of experimental measurement. Current measurement technology is able to record at both the macroscale tissue level and the microscale cellular or subcellular level, but to date it has not been possible to obtain large volume, direct measurements at the mesoscales. To bridge this scale gap in experimental measurements, we use tissue-specific structure and mathematical modeling. Our models, which can incorporate ion channel models at the cell level into the reaction-diffusion equations at the tissue level, have enabled us to consider key hypotheses regarding discontinuous activation.

@article{Aust_2006_334, abstract = {Significant tissue structures exist in cardiac ventricular tissue, which are of supracellular dimension. It is hypothesized that these tissue structures contribute to the discontinuous spread of electrical activation, may contribute to arrhythmogenesis, and also provide a substrate for effective cardioversion. However, the influences of these mesoscale tissue structures in intact ventricular tissue are difficult to understand solely on the basis of experimental measurement. Current measurement technology is able to record at both the macroscale tissue level and the microscale cellular or subcellular level, but to date it has not been possible to obtain large volume, direct measurements at the mesoscales. To bridge this scale gap in experimental measurements, we use tissue-specific structure and mathematical modeling. Our models, which can incorporate ion channel models at the cell level into the reaction-diffusion equations at the tissue level, have enabled us to consider key hypotheses regarding discontinuous activation.}, added-at = {2009-06-03T11:20:58.000+0200}, author = {Austin, Travis M and Hooks, Darren A and Hunter, Peter J and Nickerson, David P and Pullan, Andrew J and Sands, Gregory B and Smaill, Bruce H and Trew, Mark L}, biburl = {https://www.bibsonomy.org/bibtex/23d630e36a874aa7316076d9363fe5bb8/hake}, description = {The whole bibliography file I use.}, doi = {10.1196/annals.1380.025}, file = {Aust_2006_334.pdf:Aust_2006_334.pdf:PDF}, interhash = {b0081110325f2047bbcd624cfe5b40c2}, intrahash = {3d630e36a874aa7316076d9363fe5bb8}, journal = {Ann. N. Y. Acad. Sci.}, keywords = {Biological Heart; Humans; Models,}, month = Oct, pages = {334--347}, pii = {1080/1/334}, pmid = {17132793}, timestamp = {2009-06-03T11:21:01.000+0200}, title = {Modeling cardiac electrical activity at the cell and tissue levels.}, url = {http://dx.doi.org/10.1196/annals.1380.025}, volume = 1080, year = 2006 }