scholarly journals An Electric Field Mechanism for Transmission of Excitation Between Myocardial Cells

2002 ◽  
Vol 91 (11) ◽  
pp. 985-987 ◽  
Author(s):  
Nicholas Sperelakis
2003 ◽  
Vol 81 (1) ◽  
pp. 48-58 ◽  
Author(s):  
Nicholas Sperelakis

Propagation of action potentials between parallel chains of cardiac muscle cells was simulated using the PSpice program. Excitation was transmitted from cell to cell along a strand of three or four cells not connected by low-resistance tunnels (gap-junction connexons) in parallel with one or two similar strands. Thus, two models were used: a 2 × 3 model (two parallel chains of three cells each) and a 3 × 4 model (three parallel chains of four cells each). The entire surface membrane of each cell fired nearly simultaneously, and nearly all the propagation time was spent at the cell junctions, thus giving a staircase-shaped propagation profile. The junctional delay time between contiguous cells in a chain was about 0.2–0.5 ms. A significant negative cleft potential develops in the narrow junctional clefts, whose magnitude depends on several factors, including the radial cleft resistance (Rjc). The cleft potential (Vjc) depolarizes the postjunctional membrane to threshold by a patch-clamp action. Therefore, one mechanism for the transfer of excitation from one cell to the next is by the electric field (EF) that is generated in the junctional cleft when the prejunctional membrane fires. Propagation velocity increased with elevation of Rjc. With electrical stimulation of the first cell of the first strand (cell A1), propagation rapidly spread down that chain and then jumped to the second strand (B chain), followed by jumping to the third strand (C chain) when present. The rapidity by which the parallel chains became activated depended on the longitudinal resistance of the narrow extracellular cleft between the parallel strands (Rol2). The higher the Rol2 resistance, the faster the propagation (lower propagation time) over the cardiac muscle sheet (2-dimensional). The transverse resistance of the cleft had no effect. When the first cell of the second strand (cell B1) was stimulated, propagation spread down the B chain and jumped to the other two strands (A and C) nearly simultaneously. When cell C1 was stimulated, propagation traveled down the C chain and jumped to the B chain, followed by excitation of the A chain. Thus, there was transverse propagation of excitation as longitudinal propagation was occurring. Therefore, transmission of excitation by the EF mechanism can occur between myocardial cells lying closely parallel to one another without the requirement of a specialized junction.Key words: propagation in cardiac muscle, transverse propagation between myocardial cells, PSpice simulations, electric field in junctional cleft.


1978 ◽  
Vol 235 (2) ◽  
pp. H214-H222 ◽  
Author(s):  
J. L. Jones ◽  
E. Lepeschkin ◽  
R. E. Jones ◽  
S. Rush

Myocardial cells isolated from 8-day chick embryos were grown in monolayer culture under conditions that produce “standard embryonic” and “adult-type” cells. These cells were subjected to electric field stimulation that had a waveshape and intensities similar to those used in clinical electric countershock procedures. Photocell mechanograms obtained before, during, and after stimulation were correlated with simultaneously measured transmembrane potentials to determine the relationship between membrane polarization and arrhythmia production that occured after the stimulus. The results of these experiments demonstrate that a predictable sequence of mechanical responses occurs after stimuli ranging in intensity from 6 to 200 V/cm. This sequence, which closely resembles that observed in vivo after similar stimulation intensities, consists of a single response (activation), tachyarrhythmia, relaxed arrest followed by transient tachyarrhythmia, arrest with contracture, and cellular fibrillation. This diverse pattern of arrhythmias is associated with a prolonged depolarization of the cell membrane which increases with the intensity of the applied stimulus. It is probable that this depolarization is caused by a transient electromechanical deformation of the cell membrane during the shock. These findings contribute to a better understanding of the causes of the arrhythmias that appear after clinical and experimental electric countershock procedures.


1987 ◽  
Vol 253 (2) ◽  
pp. H480-H486 ◽  
Author(s):  
J. L. Jones ◽  
R. E. Jones ◽  
G. Balasky

Arrhythmias, S-T segment changes, immediate refibrillation, and other signs of dysfunction are often observed after clinical and experimental transthoracic defibrillation. In vitro studies suggested that shock-induced dysfunction is induced by sarcolemmal dielectric breakdown accompanied by ionic exchanges through transient, shock-induced microlesions in the sarcolemma. To test this hypothesis, cultured chick embryo myocardial cells were shocked in media containing fluorescein isothiocyanate-labeled dextrans (FITC-dextrans) ranging in molecular mass from 4 to 70 kDa, using electric field stimulation 5 ms in duration and ranging in intensity from 0 to 200 V/cm. Results showed that the percentage of cells incorporating 4- to 20-kDa dextrans increased in a dose-dependent manner. The 4- and 10-kDa dextrans were incorporated beginning at intensities of 50–100 V/cm. Dextran incorporation corresponded with shock intensities which produced a shock-induced arrest of spontaneous contraction lasting 1 min. The 20-kDa dextrans were incorporated following 150- and 200-V/cm shocks. Shocks of these intensities also produced a transient postshock contracture. Larger dextrans (40 and 70 kDa) were not incorporated. These results suggest the formation of transient sarcolemmal microlesions having a diameter of 45-60 A during high-intensity electric field stimulation.


2006 ◽  
Vol 24 (3) ◽  
pp. 887-900 ◽  
Author(s):  
M. Voiculescu ◽  
A. T. Aikio ◽  
T. Nygrén ◽  
J. M. Ruohoniemi

Abstract. In this paper we investigate the relationship between polar cap sporadic-E layers and the direction of the interplanetary magnetic field (IMF) using a 2-year database from Longyearbyen (75.2 CGM Lat, Svalbard) and Thule (85.4 CGM Lat, Greenland). It is found that the MLT distributions of sporadic-E occurrence are different at the two stations, but both are related to the IMF orientation. This relationship, however, changes from the centre of the polar cap to its border. Layers are more frequent during positive By at both stations. This effect is particularly strong in the central polar cap at Thule, where a weak effect associated with Bz is also observed, with positive Bz correlating with a higher occurrence of Es. Close to the polar cap boundary, at Longyearbyen, the By effect is weaker than at Thule. On the other hand, Bz plays there an equally important role as By, with negative Bz correlating with the Es occurrence. Since Es layers can be created by electric fields at high latitudes, a possible explanation for the observations is that the layers are produced by the polar cap electric field controlled by the IMF. Using electric field estimates calculated by means of the statistical APL convection model from IMF observations, we find that the diurnal distributions of sporadic-E occurrence can generally be explained in terms of the electric field mechanism. However, other factors must be considered to explain why more layers occur during positive than during negative By and why the Bz dependence of layer occurrence in the central polar cap is different from that at the polar cap boundary.


1975 ◽  
Vol 53 (22) ◽  
pp. 3419-3424 ◽  
Author(s):  
Robert J. Cushley ◽  
David Naugler ◽  
Carlos Ortiz

Formation of the N-oxide for several pyridine derivatives results in a large upfield shift of the 2-, 4-, and 6-carbons and a significant downfield shift of the 3- and 5-carbons. The chemical shifts (Δδ) are consistent with a resonance and electric field mechanism. Molecular orbital calculations using CNDO/2 show a qualitative correlation between excess charge density and Δδ.


2020 ◽  
Vol 62 (11) ◽  
pp. 2020-2023
Author(s):  
A. V. Kozyrev ◽  
V. Y. Kozhevnikov ◽  
A. O. Kokovin ◽  
V. A. Panarin ◽  
N. S. Semeniuk ◽  
...  

Author(s):  
Larry F. Lemanski ◽  
Eldridge M. Bertke ◽  
J. T. Justus

A recessive mutation has been recently described in the Mexican Axolotl, Ambystoma mexicanum; in which the heart forms structurally, but does not contract (Humphrey, 1968. Anat. Rec. 160:475). In this study, the fine structure of myocardial cells from normal (+/+; +/c) and cardiac lethal mutant (c/c) embryos at Harrison's stage 40 was compared. The hearts were fixed in a 0.1 M phosphate buffered formaldehyde-glutaraldehyde-picric acid-styphnic acid mixture and were post fixed in 0.1 M s-collidine buffered 1% osmium tetroxide. A detailed study of heart development in normal and mutant embryos from stages 25-46 will be described elsewhere.


Author(s):  
G. F. Rempfer

In photoelectron microscopy (PEM), also called photoemission electron microscopy (PEEM), the image is formed by electrons which have been liberated from the specimen by ultraviolet light. The electrons are accelerated by an electric field before being imaged by an electron lens system. The specimen is supported on a planar electrode (or the electrode itself may be the specimen), and the accelerating field is applied between the specimen, which serves as the cathode, and an anode. The accelerating field is essentially uniform except for microfields near the surface of the specimen and a diverging field near the anode aperture. The uniform field forms a virtual image of the specimen (virtual specimen) at unit lateral magnification, approximately twice as far from the anode as is the specimen. The diverging field at the anode aperture in turn forms a virtual image of the virtual specimen at magnification 2/3, at a distance from the anode of 4/3 the specimen distance. This demagnified virtual image is the object for the objective stage of the lens system.


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