We are actively pursuing a """"""""challenge-response"""""""" approach to study the mechanisms that underlie complex biological systems. In this approach, a controlled challenge is applied to the system, and its behavior is observed before, during, and after the challenge. The expectation is that well-designed challenges will cause the system to behave in a way exposes the underlying mechanism. This project is concerned with the designing the challenges that elicit the most informative behaviors. As an example of this approach, our group has quantified an association between cardiac electrophysiology and cardiac metabolism using a series of measurements on isolated rabbit hearts. We observed the time course of cardiac action potential duration (APD) as a result of intermittent cardiac anoxia, a metabolic challenge that simulates asphyxia. Evidence from these experiments support our hypothesis that supplementation with glutamine and glutamate mitigates the reduction in APD associated with cardiac anoxia. Our next challenge is to develop a framework for mechanism discovery, using mathematical models of alternative mechanisms, and to design the challenge-response experiments that best distinguish among the alternatives. Statistical methods for estimation, inference, and research design in the context of mechanistic models are a patchwork from the literature on mathematical modeling, nonlinear regression, longitudinal analysis, and model selection. There is a need to unify and tailor the methodology in this context, and to seriously consider the data complexities that commonly arise in challenge-response experiments, for example, discontinuous and nonlinear trends, heteroscedasticity in time, and nested sources of residual error. The optimal design methods that perform best under these complexities are unknown. The proposed work addresses this issue, by considering innovative approaches to optimal design in simulated in-silico studies, and using experiments with isolated rabbit hearts. Given two mechanistic models of challenge-response behavior, the experimental challenge may be tailored to discriminate between the two mechanisms. Challenge-response experiments are unique because the design parameters (e.g., the type, duration, and intensity of challenge) modify the response in a predictable way. Hence, these """"""""active"""""""" design parameters are optimized such that the predicted responses are most divergent among the competing mechanistic models. We anticipate that optimal research design using both """"""""active"""""""" and """"""""passive"""""""" design parameters (e.g., the number and spacing of measurements in time) will accelerate biomedical discovery, and reduce the associated costs. We propose to study and experimentally validate an optimal design methodology in the context of challenge- experiments for the purpose of mechanistic model discrimination. We will simultaneously address three important questions in the modeling of cardiac electrophysiology.
We anticipate that the biostatistical and experimental design strategies produced by this work will accelerate biomedical discovery in the study of complex biological systems, and reduce the associated costs (e.g. financial, human, laboratory animal). In addition, this research will address specific scientific questions that arise in our effort to understand cardiac electrophysiology and related therapeutics, such as cardiac defibrillation.
|Schroer, Alison K; Shotwell, Matthew S; Sidorov, Veniamin Y et al. (2017) I-Wire Heart-on-a-Chip II: Biomechanical analysis of contractile, three-dimensional cardiomyocyte tissue constructs. Acta Biomater 48:79-87|
|Galappaththige, Suran K; Gray, Richard A; Roth, Bradley J (2017) Cardiac strength-interval curves calculated using a bidomain tissue with a parsimonious ionic current. PLoS One 12:e0171144|
|Sidorov, Veniamin Y; Samson, Philip C; Sidorova, Tatiana N et al. (2017) I-Wire Heart-on-a-Chip I: Three-dimensional cardiac tissue constructs for physiology and pharmacology. Acta Biomater 48:68-78|
|Galappaththige, Suran K; Gray, Richard A; Roth, Bradley J (2017) Modeling bipolar stimulation of cardiac tissue. Chaos 27:093920|
|Shotwell, Matthew S; Zhou, Minchun; Fissell, William H (2016) Optimal design of perturbations for individual two-compartment pharmacokinetic analysis. J Biopharm Stat 26:803-15|
|Shotwell, Matthew S; Gray, Richard A (2016) Estimability Analysis and Optimal Design in Dynamic Multi-scale Models of Cardiac Electrophysiology. J Agric Biol Environ Stat 21:261-276|
|Galappaththige, Suran; Roth, Bradley J (2015) Electrical Pacing of Cardiac Tissue Including Potassium Inward Rectification. PLoS One 10:e0127837|
|Pathmanathan, Pras; Shotwell, Matthew S; Gavaghan, David J et al. (2015) Uncertainty quantification of fast sodium current steady-state inactivation for multi-scale models of cardiac electrophysiology. Prog Biophys Mol Biol 117:4-18|
|Drake, Kenneth J; Shotwell, Matthew S; Wikswo, John P et al. (2015) Glutamine and glutamate limit the shortening of action potential duration in anoxia-challenged rabbit hearts. Physiol Rep 3:|
|Kandel, Sunil M; Roth, Bradley J (2015) ELECTRICAL INSTABILITY DUE TO REGIONAL INCREASE IN EXTRACELLULAR POTASSIUM ION CONCENTRATION. J Nat Sci 1:|
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