ten Tusscher, Panfilov, 2006

Model Status

This is the EPICARDIAL CELL VARIANT of the model. This model was created by Penny Noble of Oxford University and is known to read in COR and PCEnv. A stimulus protocol has been added that allows the model to simulate multiple action potentials at 1Hz.

Model Structure

In their 2006 paper "Alternans and spiral breakup in a human ventricular tissue model," ten Tusscher et al. improve the detail of their 2004 model in order to investigate the conditions for electrical instability in human ventricular tissue by simulation. In particular, the so-called 'resitution hypothesis' of ventricular fibrillation, which states that if the action potential duration (APD) restitution curve has a maximum slope steeper than 1, it will lead to APD alternans. Because of the substantial limitations of using traditional experimental electrophysiological techniques to investigate these phenomena, mathematical modelling is a useful technique for such studies. The 2006 model is based on earlier ten Tusscher models, and incorporates recent experimental restitution data, an improved description of intracellular calcium dynamics - including subspace calcium dynamics which control L-type calcium current and calcium-induced calcium release (CICR,) by means of modelling CICR with a four-state Markov model for the ryanodine receptor - and incorporation of both fast and slow voltage-gated inactivation of the L-type calcium current.

ABSTRACT:

Ventricular fibrillation (VF) is one of the main causes of death in the Western world. According to one hypothesis, the chaotic excitation dynamics during VF are the result of dynamical instabilities in action potential duration (APD) the occurrence of which requires that the slope of the APD restitution curve exceeds 1. Other factors such as electrotonic coupling and cardiac memory also determine whether these instabilities can develop. In this paper we study the conditions for alternans and spiral breakup in human cardiac tissue. Therefore, we develop a new version of our human ventricular cell model, which is based on recent experimental measurements of human APD restitution and includes a more extensive description of intracellular calcium dynamics. We apply this model to study the conditions for electrical instability in single cells, for reentrant waves in a ring of cells, and for reentry in two-dimensional sheets of ventricular tissue. We show that an important determinant for the onset of instability is the recovery dynamics of the fast sodium current. Slower sodium current recovery leads to longer periods of spiral wave rotation and more gradual conduction velocity restitution, both of which suppress restitution-mediated instability. As a result, maximum restitution slopes considerably exceeding 1 (up to 1.5) may be necessary for electrical instability to occur. Although slopes necessary for the onset of instabilities found in our study exceed 1, they are within the range of experimentally measured slopes. Therefore, we conclude that steep APD restitution-mediated instability is a potential mechanism for VF in the human heart.

The complete original paper reference is cited below:

Alternans and spiral breakup in a human ventricular tissue model, K.H.W.J. ten Tusscher, A.V. Panfilov, Sep 2006, American Journal of Physiology, Heart and Circulatory Physiology , 291 3, H1088-1100. (Full text (HTML) and PDF versions of the article are available to subscribers on the American Journal of Physiology website.) PubMed ID: 16565318

A schematic diagram describing the ion movement across the cell surface membrane and the sarcoplasmic reticulum, which are described by the Ten Tusscher et al. 2006 mathematical model of the human ventricular myocyte.
Source
Derived from workspace Tentusscher, Panfilov, 2006 at changeset e8edfb3822b1.
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