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Extracellular Perinexal Separation Is a Principal Determinant of Cardiac Conduction.
Adams, William P; Raisch, Tristan B; Zhao, Yajun; Davalos, Rafael; Barrett, Sarah; King, D Ryan; Bain, Chandra B; Colucci-Chang, Katrina; Blair, Grace A; Hanlon, Alexandra; Lozano, Alicia; Veeraraghavan, Rengasayee; Wan, Xiaoping; Deschenes, Isabelle; Smyth, James W; Hoeker, Gregory S; Gourdie, Robert G; Poelzing, Steven.
Affiliation
  • Adams WP; Center for Vascular and Heart Research at Fralin Biomedical Research Institute at VTC (W.P.A., T.B.R., D.R.K., C.B.B., K.C.-C., G.A.B., J.W.S., G.S.H., R.G.G., S.P.).
  • Raisch TB; Translational Biology, Medicine and Health Program at Virginia Tech (W.P.A., T.B.R., D.R.K., G.A.B., S.P.).
  • Zhao Y; Center for Vascular and Heart Research at Fralin Biomedical Research Institute at VTC (W.P.A., T.B.R., D.R.K., C.B.B., K.C.-C., G.A.B., J.W.S., G.S.H., R.G.G., S.P.).
  • Davalos R; Translational Biology, Medicine and Health Program at Virginia Tech (W.P.A., T.B.R., D.R.K., G.A.B., S.P.).
  • Barrett S; School of Biomedical Engineering and Sciences, Virginia Tech (Y.Z., R.D., K.C.-C., R.G.G., S.P.).
  • King DR; School of Biomedical Engineering and Sciences, Virginia Tech (Y.Z., R.D., K.C.-C., R.G.G., S.P.).
  • Bain CB; Virginia-Maryland College of Veterinary Medicine (S.B.).
  • Colucci-Chang K; Center for Vascular and Heart Research at Fralin Biomedical Research Institute at VTC (W.P.A., T.B.R., D.R.K., C.B.B., K.C.-C., G.A.B., J.W.S., G.S.H., R.G.G., S.P.).
  • Blair GA; Translational Biology, Medicine and Health Program at Virginia Tech (W.P.A., T.B.R., D.R.K., G.A.B., S.P.).
  • Hanlon A; Center for Vascular and Heart Research at Fralin Biomedical Research Institute at VTC (W.P.A., T.B.R., D.R.K., C.B.B., K.C.-C., G.A.B., J.W.S., G.S.H., R.G.G., S.P.).
  • Lozano A; Center for Vascular and Heart Research at Fralin Biomedical Research Institute at VTC (W.P.A., T.B.R., D.R.K., C.B.B., K.C.-C., G.A.B., J.W.S., G.S.H., R.G.G., S.P.).
  • Veeraraghavan R; School of Biomedical Engineering and Sciences, Virginia Tech (Y.Z., R.D., K.C.-C., R.G.G., S.P.).
  • Wan X; Center for Vascular and Heart Research at Fralin Biomedical Research Institute at VTC (W.P.A., T.B.R., D.R.K., C.B.B., K.C.-C., G.A.B., J.W.S., G.S.H., R.G.G., S.P.).
  • Deschenes I; Translational Biology, Medicine and Health Program at Virginia Tech (W.P.A., T.B.R., D.R.K., G.A.B., S.P.).
  • Smyth JW; Virginia Tech Center for Biostatistics and Health Data Science, Roanoke (A.H., A.L.).
  • Hoeker GS; Virginia Tech Center for Biostatistics and Health Data Science, Roanoke (A.H., A.L.).
  • Gourdie RG; Department of Biomedical Engineering, College of Engineering, The Ohio State University (R.V.).
  • Poelzing S; The Frick Center for Heart Failure and Arrhythmia, Dorothy M. Davis Heart and Lung Research Institute, College of Medicine, The Ohio State University Wexner Medical Center (R.V., X.W., I.D.).
Circ Res ; 133(8): 658-673, 2023 09 29.
Article in En | MEDLINE | ID: mdl-37681314
ABSTRACT

BACKGROUND:

Cardiac conduction is understood to occur through gap junctions. Recent evidence supports ephaptic coupling as another mechanism of electrical communication in the heart. Conduction via gap junctions predicts a direct relationship between conduction velocity (CV) and bulk extracellular resistance. By contrast, ephaptic theory is premised on the existence of a biphasic relationship between CV and the volume of specialized extracellular clefts within intercalated discs such as the perinexus. Our objective was to determine the relationship between ventricular CV and structural changes to micro- and nanoscale extracellular spaces.

METHODS:

Conduction and Cx43 (connexin43) protein expression were quantified from optically mapped guinea pig whole-heart preparations perfused with the osmotic agents albumin, mannitol, dextran 70 kDa, or dextran 2 MDa. Peak sodium current was quantified in isolated guinea pig ventricular myocytes. Extracellular resistance was quantified by impedance spectroscopy. Intercellular communication was assessed in a heterologous expression system with fluorescence recovery after photobleaching. Perinexal width was quantified from transmission electron micrographs.

RESULTS:

CV primarily in the transverse direction of propagation was significantly reduced by mannitol and increased by albumin and both dextrans. The combination of albumin and dextran 70 kDa decreased CV relative to albumin alone. Extracellular resistance was reduced by mannitol, unchanged by albumin, and increased by both dextrans. Cx43 expression and conductance and peak sodium currents were not significantly altered by the osmotic agents. In response to osmotic agents, perinexal width, in order of narrowest to widest, was albumin with dextran 70 kDa; albumin or dextran 2 MDa; dextran 70 kDa or no osmotic agent, and mannitol. When compared in the same order, CV was biphasically related to perinexal width.

CONCLUSIONS:

Cardiac conduction does not correlate with extracellular resistance but is biphasically related to perinexal separation, providing evidence that the relationship between CV and extracellular volume is determined by ephaptic mechanisms under conditions of normal gap junctional coupling.
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Full text: 1 Database: MEDLINE Main subject: Dextrans / Connexin 43 Limits: Animals Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Dextrans / Connexin 43 Limits: Animals Language: En Year: 2023 Type: Article