Electrophysiological Effects of Remodeling Cardiac Gap Junctions and Cell Size

Author:

Spach Madison S.1,Heidlage J. Francis1,Dolber Paul C.1,Barr Roger C.1

Affiliation:

1. From the Departments of Pediatrics (M.S.S., J.F.H.), Cell Biology (M.S.S.), and Biomedical Engineering (R.C.B.), Duke University Medical Center, and Department of Surgery (P.C.D.), Veterans Affairs Medical Center, Durham, NC.

Abstract

Abstract —The increased incidence of arrhythmias in structural heart disease is accompanied by remodeling of the cellular distribution of gap junctions to a diffuse pattern like that of neonatal cardiomyocytes. Accordingly, it has become important to know how remodeling of gap junctions due to normal growth hypertrophy alters anisotropic propagation at a cellular level (V̇ max ) in relation to conduction velocities measured at a macroscopic level. To this end, morphological studies of gap junctions (connexin43) and in vitro electrical measurements were performed in neonatal and adult canine ventricular muscle. When cells enlarged, gap junctions shifted from the sides to the ends of ventricular myocytes. Electrically, normal growth produced different patterns of change at a macroscopic and microscopic level. Although the longitudinal and transverse conduction velocities were greater in adult than neonatal muscle, the anisotropic velocity ratios were the same. In the neonate, mean V̇ max was not different during longitudinal (LP) and transverse (TP) propagation. However, growth hypertrophy produced a selective increase in mean TP V̇ max ( P <0.001), with no significant change in mean LP V̇ max . Two-dimensional neonatal and adult cellular computational models show that the observed increases in cell size and changes in the distribution of gap junctions are sufficient to account for the experimental results. Unexpectedly, the results show that cellular scaling (cell size) is as important (or more so) as changes in gap junction distribution in determining TP properties. As the cells enlarged, both mean TP V̇ max and lateral cell-to-cell delay increased. V̇ max increased because increases in cell-to-cell delay reduced the electric current flowing downstream up to the time of V̇ max , thus enhancing V̇ max . The results suggest that in pathological substrates that are arrhythmogenic, maintaining cell size during remodeling of gap junctions is important in sustaining a maximum rate of depolarization.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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