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An ionically based mapping model with memory for cardiac restitution

  • David G. Schaeffer
  • , John W. Cain
  • , Daniel J. Gauthier
  • , Soma S. Kalb
  • , Robert A. Oliver
  • , Elena G. Tolkacheva
  • , Wenjun Ying
  • , Wanda Krassowska

Research output: Contribution to journalArticlepeer-review

Abstract

Many features of the sequence of action potentials produced by repeated stimulation of a patch of cardiac muscle can be modeled by a 1D mapping, but not the full behavior included in the restitution portrait. Specifically, recent experiments have found that (i) the dynamic and S1-S2 restitution curves are different (rate dependence) and (ii) the approach to steady state, which requires many action potentials (accommodation), occurs along a curve distinct from either restitution curve. Neither behavior can be produced by a 1D mapping. To address these shortcomings, ad hoc 2D mappings, where the second variable is a "memory" variable, have been proposed; these models exhibit qualitative features of the relevant behavior, but a quantitative fit is not possible. In this paper we introduce a new 2D mapping and determine a set of parameters for it that gives a quantitatively accurate description of the full restitution portrait measured from a bullfrog ventricle. The mapping can be derived as an asymptotic limit of an idealized ionic model in which a generalized concentration acts as a memory variable. This ionic basis clarifies how the present model differs from previous models. The ionic basis also provides the foundation for more extensive cardiac modeling: e.g., constructing a PDE model that may be used to study the effect of memory on propagation. The fitting procedure for the mapping is straightforward and can easily be applied to obtain a mathematical model for data from other experiments, including experiments on different species.

Original languageEnglish (US)
Pages (from-to)459-482
Number of pages24
JournalBulletin of Mathematical Biology
Volume69
Issue number2
DOIs
StatePublished - Feb 2007

Bibliographical note

Funding Information:
The Support of the National Institutes of Health under grant 1R01-HL-72831 and the National Science Foundation under grants PHY-0243584 and DMS-9983320 is gratefully acknowledged.

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