Location: Aslanidi_etal_2010 @ f9e156454803 / Aslanidi_etal_2010.html

Author:
Dougal Cowan <devnull@localhost>
Date:
2012-06-19 14:50:18+12:00
Desc:
edited model links
Permanent Source URI:
https://models.cellml.org/w/dcowan/Aslanidi_etal_2010/rawfile/f9e1564548039eb6ee890cb9463d897ae8a732da/Aslanidi_etal_2010.html

Model Status

These models represent rabbit ventricular Purkinje, endocardial, midmyocardial, and epicardial cells. Original code in C provided. The models will be converted to CellML and a new exposure made at that time.

Model Code Files

Purkinje cell model

Endocardial cell model

Midmyocardial cell model

Epicardial cell model

Model Structure

ABSTRACT: The intrinsic heterogeneity of electrical action potential (AP) properties between Purkinje fibers (PFs) and the ventricular wall, as well as within the wall, plays an important role in ensuring successful excitation of the ventricles. It can also be proarrhythmic due to nonuniform repolarization across the Purkinje-ventricular junction. However, the ionic mechanisms that underlie the marked AP differences between PFs and ventricular cells are not fully characterized. We studied such mechanisms by developing a new family of biophysically detailed AP models for rabbit PF cells and three transmural ventricular cell types. The models were based on and validated against experimental data recorded from rabbit at ionic channel, single cell, and tissue levels. They were then used to determine the functional roles of each individual ionic channel current in modulating the AP heterogeneity at the rabbit Purkinje-ventricular junction, and to identify specific currents responsible for the differential response of PFs and ventricular cells to pharmacological interventions.

The original paper reference is cited below:

Ionic mechanisms for electrical heterogeneity between rabbit Purkinje fiber and ventricular cells, Oleg V Aslanidi, Rakan N Sleiman, Mark R Boyett, Jules C Hancox and Henggui Zhang, 2010 Biophysical Journal, 98, 2420-31. PubMed ID: 20513385>