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Electrical communication in the heart is crucial for maintaining normal cardiac function. Traditionally, gap junctional coupling between cardiomyocytes has been accepted as the primary mechanism governing electrical propagation in the heart. However, numerous studies have demonstrated that gap junctions are also present between different cell types in heterocellular structures and disruption of such gap junctional coupling can be associated with cardiac dysfunction. In addition to gap junctional coupling, ephaptic coupling has been proposed as another mechanism for electrical communication between cardiomyocytes. Reducing ephaptic coupling has been shown to have negative impacts on cardiac conduction. While the existence of ephaptic coupling between different types of cardiac cell is under investigation, a recent study suggests that ephaptic coupling at heterocellular contacts between cardiomyocytes and fibroblasts may provide a proarrhythmic substrate in cardiac disease. In this review, we examine the current literature on electrical communication in the heart, including gap junctional and ephaptic coupling in homocellular and heterocellular contexts. Further, we offer a perspective on gaps in knowledge and opportunities for further advancing our understanding of electrical coupling mechanisms in action potential propagation in the heart.
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http://dx.doi.org/10.1113/JP287358 | DOI Listing |
MethodsX
December 2025
Center for Brain, Mind and KANSEI Sciences Research, Hiroshima University, Hiroshima, Hiroshima 734-8551, Japan.
As the working hypothesis in the present study, neural coupling (NC) is the sum of synaptic coupling (SC) and volume current coupling (VcC), and VcC influences cognitive and behavioral functions. VcC is a remote direct electrical coupling, or electrical crosstalk, across extracellular space between electroencephalogram (EEG) generators, which are spatiotemporally synchronously activated pyramidal neural populations. VcCs can occur everywhere in the brain along volume current (Vc) propagation paths.
View Article and Find Full Text PDFPLoS One
August 2025
Department of Biomedical Engineering, University of Minnesota, 312 Church St SE, Minneapolis, Minnesota, United States of America.
Cardiac myocytes synchronize through electrical signaling to contract heart muscles, facilitated by gap junctions (GJs) located in the intercalated disc (ID). GJs provide low-resistance pathways for electrical impulse propagation between myocytes, considered the primary mechanism for electrical communication in the heart. However, research indicates that conduction can persist without GJs.
View Article and Find Full Text PDFBiophys J
August 2025
University of Pennsylvania, Department of Mathematics and Department of Biology, David Rittenhouse Laboratory, Philadelphia, Pennsylvania.
Cardiac myocytes coordinate the heart contractions through electrical signaling, facilitated by gap junctions (GJs) in the intercalated disk. GJs provide low-resistance pathways for electrical propagation between myocytes, acting as the main mechanism for electrical communication in the heart. However, studies show that conduction can persist in the absence of GJs.
View Article and Find Full Text PDFJ Physiol
May 2025
Center for Heart and Reparative Medicine Research, Fralin Biomedical Research Institute at Virginia Tech Carilion, Roanoke, Virginia, USA.
Electrical communication in the heart is crucial for maintaining normal cardiac function. Traditionally, gap junctional coupling between cardiomyocytes has been accepted as the primary mechanism governing electrical propagation in the heart. However, numerous studies have demonstrated that gap junctions are also present between different cell types in heterocellular structures and disruption of such gap junctional coupling can be associated with cardiac dysfunction.
View Article and Find Full Text PDFHeart Rhythm
April 2025
Fralin Biomedical Research Institute at Virginia Tech Carilion, Center for Vascular and Heart Research, Roanoke, Virginia; Department of Biomedical Engineering and Mechanics, Virginia Polytechnic Institute and State University, Blacksburg, Virginia. Electronic address:
Background: Studies suggest that voltage-gated sodium channel (SC) loss-of-function (LoF), often through the use of SC blockers, such as tricyclic anti-depressants, some recreational drugs, and importantly, class 1c anti-arrhythmics, sensitizes cardiac conduction to hyponatremia. However, the mechanism driving conduction velocity (CV) sensitivity to sodium ion (Na) concentration ([Na]) is unknown. We recently demonstrated CV-[Na] sensitivity in haploinsufficient Scn5a+/- mouse and reduced CV-[Na] sensitivity when ephaptic coupling (extracellular conduction by electric fields) is also reduced.
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