Changes in anisotropic conduction caused by remodeling cell size and the cellular distribution of gap junctions and Na+ channels

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

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Because gene therapy presents a new frontier in the treatment of arrhythmias, it has become important to know how manipulation of the cellular distribution of proteins changes electrical events within individual cells, and whether these cellular changes affect conduction at the larger macroscopic size scale. However, experimental limitations in cardiac bundles prevent measurement of conduction delays across specific gap junctions, as well as the intracellular distribution of the maximum rate of rise of the action potential (Vmax). In view of these limitations, we used immunohistochemical morphological results as a basis to develop two-dimensional cellular models of neonatal and mature canine ventricular muscle in order to obtain insight into the electrophysiological effects of changes in the cellular distribution of proteins; eg, the major protein of cardiac gap junctions, connexin43. Morphological results showed that when the cells enlarged after birth, the gap junctions shifted from the sides to the ends of ventricular myocytes. At birth, Vmax was not different during longitudinal and transverse propagation. However, growth hypertrophy produced a selective increase in mean transverse Vmax with no significant change in longitudinal Vmax. Two-dimensional cellular computational models of neonatal and mature ventricular muscle showed that the observed changes in the cellular distribution of the gap junctions and change in cell size accounted for the experimental results. The results unexpectedly showed that cellular scaling (cell size) is as important (or more so) as changes in gap junction distribution in determining the properties of transverse propagation. The results suggest that in pathological states that are arrhythmogenic, maintenance of cell size during remodeling the distribution of gap junctions is important in sustaining a maximum rate of rise of the action potential.

Original languageEnglish (US)
Pages (from-to)69-76
Number of pages8
JournalJournal of Electrocardiology
Volume34
Issue numberSUPPL.
DOIs
StatePublished - 2001
Externally publishedYes

Fingerprint

Gap Junctions
Cell Size
Action Potentials
Parturition
Muscles
Connexin 43
Connexins
Genetic Therapy
Muscle Cells
Hypertrophy
Canidae
Cardiac Arrhythmias
Proteins
Maintenance
Growth

Keywords

  • Anisotropic propagation
  • Cellular size
  • Gap junctions
  • Structural remoleling
  • V

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Changes in anisotropic conduction caused by remodeling cell size and the cellular distribution of gap junctions and Na+ channels. / Spach, Madison S.; Heidlage, J. Francis; Dolber, Paul C.; Barr, Roger C.

In: Journal of Electrocardiology, Vol. 34, No. SUPPL., 2001, p. 69-76.

Research output: Contribution to journalArticle

Spach, Madison S. ; Heidlage, J. Francis ; Dolber, Paul C. ; Barr, Roger C. / Changes in anisotropic conduction caused by remodeling cell size and the cellular distribution of gap junctions and Na+ channels. In: Journal of Electrocardiology. 2001 ; Vol. 34, No. SUPPL. pp. 69-76.
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