Growing evidence suggests that the discrete coupling, cellular architecture and heterogeneities at multiple spatial scales play a major role in the initiation, maintenance and termination of arrhythmia under certain diseased conditions and particularly during aging. Consequently, the development of appropriate and effective antiarrhythmic pharmacological or biological therapies requires a better understanding of the factors that modulate impulse propagation in a heterogeneous substrate in critical regimes where conduction can fail. In particular, this proposal seeks to answer the following fundamental questions: 1) Is it necessary to model diseased tissue substrates with micro-heterogeneity using micro-structural models or can the dynamics of interest can be captured using continuous models, as is now the practice?;2) How and why are impulse conduction and reentry dynamics altered in the context of structural heart disease?;and 3) Does tailoring the basic electrical properties of introduced/altered non- myocytes within diseased cardiac tissue could improve conduction and prevent reentry induction? We plan to use the predictive properties of the validated model to inform future experiments and inspire a rational approach for designing novel antiarrhythmic therapies.
The aims are 1) To develop and refine a parameter estimation technique to derive the microscale electrical properties of a monolayer of neonatal rat cells and to use the combined computational/experimental approach to investigate the effects of cell orientations and patterns of cell coupling on microscopic impulse conduction in a geometrically controlled structural setting. 2) To use a combined theoretical/experimental framework to develop a diseased model of cardiac tissue to investigate the roles of conduction barriers and heterogeneous tissue structure on impulse conduction and reentry dynamics in a geometrically controlled structural setting. 3) To use the framework in Aim 1 to study the effect of non-myocytes on cardiac impulse conduction and reentry dynamics in a geometrically controlled structural setting, and to use the models to develop therapeutic strategies to facilitate conduction. The methods proposed here will allow us to create computer models that have one-to-one correspondence with the monolayers with regard to cell shape and cell-to-cell connectivity. Once validated, the models will be extended to adult architectures and diseased tissue for which it is not currently possible to develop engineered tissue. Ultimately these models will be used as a testbed to design new experiments to study the role of heterogeneity on arrhythmia and develop novel approaches for reengineering the arrhythmogenic substrate either through novel cell therapies or new drugs.
An estimated 400,000 Americans die each year from erratic heart rhythms, and many more are disabled (estimated annual fatalities worldwide is seven million). The proposed research is aimed at developing predictive computer models of heart tissue to test and screen novel therapies.
|Gokhale, Tanmay A; Kim, Jong M; Kirkton, Robert D et al. (2017) Modeling an Excitable Biosynthetic Tissue with Inherent Variability for Paired Computational-Experimental Studies. PLoS Comput Biol 13:e1005342|
|Gokhale, Tanmay A; Medvescek, Eli; Henriquez, Craig S (2017) Modeling dynamics in diseased cardiac tissue: Impact of model choice. Chaos 27:093909|
|Hubbard, Marjorie Letitia; Henriquez, Craig S (2014) A microstructural model of reentry arising from focal breakthrough at sites of source-load mismatch in a central region of slow conduction. Am J Physiol Heart Circ Physiol 306:H1341-52|
|Henriquez, Craig S (2014) A brief history of tissue models for cardiac electrophysiology. IEEE Trans Biomed Eng 61:1457-65|
|Hubbard, Marjorie Letitia; Henriquez, Craig S (2012) Microscopic variations in interstitial and intracellular structure modulate the distribution of conduction delays and block in cardiac tissue with source-load mismatch. Europace 14 Suppl 5:v3-v9|
|Scull, James A; McSpadden, Luke C; Himel 4th, Herman D et al. (2012) Single-detector simultaneous optical mapping of V(m) and [Ca(2+)](i) in cardiac monolayers. Ann Biomed Eng 40:1006-17|
|Stinstra, Jeroen; MacLeod, Rob; Henriquez, Craig (2010) Incorporating histology into a 3D microscopic computer model of myocardium to study propagation at a cellular level. Ann Biomed Eng 38:1399-414|
|Hubbard, Marjorie Letitia; Henriquez, Craig S (2010) Increased interstitial loading reduces the effect of microstructural variations in cardiac tissue. Am J Physiol Heart Circ Physiol 298:H1209-18|
|Kim, Jong M; Bursac, Nenad; Henriquez, Craig S (2010) A computer model of engineered cardiac monolayers. Biophys J 98:1762-71|