Spatial Changes in Transmembrane Potential During Extracellular Electrical Shocks in Cultured Monolayers of Neonatal Rat Ventricular Myocytes
- 1 October 1996
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 79 (4) , 676-690
- https://doi.org/10.1161/01.res.79.4.676
Abstract
This study investigated the role of different types of discontinuities in tissue architecture on the spatial distribution of the transmembrane potential. Specifically, we tested the occurrence of so-called “secondary sources,” ie, localized hyperpolarizations and depolarizations during the application of extracellular electrical shocks (EESs). Changes in transmembrane potential relative to action potential amplitude (ΔVm/APA) were measured in patterned cultures of neonatal rat myocytes, stained with voltage-sensitive dye (RH-237), by optical mapping (96-channel photodiode array, 6- to 30-μm resolution) during the application of EES (field strength, 8 to 22 V/cm; duration, 6 ms). Across narrow cell strands (width, 218±59 [mean±SD] μm), EES applied during the relative refractory period produced a linear and symmetrical profile of ΔVm/APA (−65±23% maximal hyperpolarization versus +64±15% maximal depolarization). In contrast, the profile of ΔVm/APA was asymmetrical when EESs were applied during the action potential plateau (−95±32% versus +37±14%). At high magnification, no secondary sources were observed at the borders between cells. In dense isotropic cell monolayers or in monolayers and strands showing intercellular clefts, secondary sources were frequently observed. Intercellular clefts of the size of one to several myocytes were sufficient to produce secondary sources of the same magnitude as those that elicited action potentials in dense cell strands. There was a close correlation between the location of secondary sources during EES and localized conduction slowing during propagation. Thus, densely packed cultured cell strands behave as an electrical continuum with no secondary sources occurring at cell borders. Small intercellular clefts can create secondary sources of sufficient magnitude to exert a stimulatory effect.Keywords
This publication has 20 references indexed in Scilit:
- Virtual electrodes in cardiac tissue: a common mechanism for anodal and cathodal stimulationBiophysical Journal, 1995
- Determination of Impulse Conduction Characteristics at a icroscopic Scale in Patterned Growth Heart Cell ultures Using Multiple Site Optical Recording of Transmemhrane VoltageJournal of Cardiovascular Electrophysiology, 1995
- Responses of the Transmembrane Potential of Myocardial Cells during a ShocksJournal of Cardiovascular Electrophysiology, 1995
- Multiple site optical recording of transmembrane voltage (MSORTV) in patterned growth heart cell cultures: assessing electrical behavior, with microsecond resolution, on a cellular and subcellular scaleBiophysical Journal, 1994
- A Novel Technique for the Study of Intercellular, Junctional Communication: Electroporation of Adherent Cells on a Partly Conductive SlideDNA and Cell Biology, 1994
- Remodeling of ventricular conduction pathways in healed canine infarct border zones.Journal of Clinical Investigation, 1991
- Conservation of a cytoplasmic carboxy-terminal domain of connexin 43, a gap junctional protein, in mammal heart and brainThe Journal of Membrane Biology, 1990
- Termination of ventricular fibrillation in dogs by depolarizing a critical amount of myocardiumThe American Journal of Cardiology, 1975
- Electrotonic spread of current in monolayer cultures of neonatal rat heart cellsThe Journal of Membrane Biology, 1972
- The electrical constants of a crustacean nerve fibreProceedings of the Royal Society of London. B. Biological Sciences, 1946