Cargando…

Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations

BACKGROUND: We previously examined transverse propagation of action potentials between 2 and 3 parallel chain of cardiac muscle cells (CMC) simulated using the PSpice program. The present study was done to examine transverse propagation between 5 parallel chains in an expanded model of CMC and smoot...

Descripción completa

Detalles Bibliográficos
Autores principales: Sperelakis, Nicholas, Kalloor, Bijoy
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC400751/
https://www.ncbi.nlm.nih.gov/pubmed/14998434
http://dx.doi.org/10.1186/1475-925X-3-5
_version_ 1782121371263827968
author Sperelakis, Nicholas
Kalloor, Bijoy
author_facet Sperelakis, Nicholas
Kalloor, Bijoy
author_sort Sperelakis, Nicholas
collection PubMed
description BACKGROUND: We previously examined transverse propagation of action potentials between 2 and 3 parallel chain of cardiac muscle cells (CMC) simulated using the PSpice program. The present study was done to examine transverse propagation between 5 parallel chains in an expanded model of CMC and smooth muscle cells (SMC). METHODS: Excitation was transmitted from cell to cell along a strand of 5 cells not connected by low-resistance tunnels (gap-junction connexons). The entire surface membrane of each cell fired nearly simultaneously, and nearly all the propagation time was spent at the cell junctions, the junctional delay time being about 0.3 – 0.5 ms (CMC) or 0.8 – 1.6 ms (SMC). A negative cleft potential (V(jc)) develops in the narrow junctional clefts, whose magnitude depends on the radial cleft resistance (R(jc)), which depolarizes the postjunctional membrane (post-JM) to threshold. Propagation velocity (θ) increased with amplitude of V(jc). 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 pre-JM fires. In the present study, 5 parallel stands of 5 cells each (5 × 5 model) were used. RESULTS: 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, fourth, and fifth strands (C, D, E chains). The rapidity by which the parallel chains became activated depended on the longitudinal resistance of the narrow extracellular cleft between the parallel strands (R(ol2)); the higher the R(ol2 )resistance, the faster the θ. The transverse resistance of the cleft (R(or2)) had almost no effect. Increasing R(jc )decreases the total propagation time (TPT) over the 25-cell network. When the first cell of the third strand (cell C1) was stimulated, propagation spread down the C chain and jumped to the other two strands (B and D) nearly simultaneously. CONCLUSIONS: Transverse propagation of excitation occurred at multiple points along the chain as longitudinal propagation was occurring, causing the APs in the contiguous chains to become bunched up. Transverse propagation was more erratic and labile in SMC compared to CMC. Transverse transmission of excitation did not require low-resistance connections between the chains, but instead depended on the value of R(ol2). The tighter the packing of the chains facilitated transverse propagation.
format Text
id pubmed-400751
institution National Center for Biotechnology Information
language English
publishDate 2004
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-4007512004-05-02 Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations Sperelakis, Nicholas Kalloor, Bijoy Biomed Eng Online Research BACKGROUND: We previously examined transverse propagation of action potentials between 2 and 3 parallel chain of cardiac muscle cells (CMC) simulated using the PSpice program. The present study was done to examine transverse propagation between 5 parallel chains in an expanded model of CMC and smooth muscle cells (SMC). METHODS: Excitation was transmitted from cell to cell along a strand of 5 cells not connected by low-resistance tunnels (gap-junction connexons). The entire surface membrane of each cell fired nearly simultaneously, and nearly all the propagation time was spent at the cell junctions, the junctional delay time being about 0.3 – 0.5 ms (CMC) or 0.8 – 1.6 ms (SMC). A negative cleft potential (V(jc)) develops in the narrow junctional clefts, whose magnitude depends on the radial cleft resistance (R(jc)), which depolarizes the postjunctional membrane (post-JM) to threshold. Propagation velocity (θ) increased with amplitude of V(jc). 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 pre-JM fires. In the present study, 5 parallel stands of 5 cells each (5 × 5 model) were used. RESULTS: 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, fourth, and fifth strands (C, D, E chains). The rapidity by which the parallel chains became activated depended on the longitudinal resistance of the narrow extracellular cleft between the parallel strands (R(ol2)); the higher the R(ol2 )resistance, the faster the θ. The transverse resistance of the cleft (R(or2)) had almost no effect. Increasing R(jc )decreases the total propagation time (TPT) over the 25-cell network. When the first cell of the third strand (cell C1) was stimulated, propagation spread down the C chain and jumped to the other two strands (B and D) nearly simultaneously. CONCLUSIONS: Transverse propagation of excitation occurred at multiple points along the chain as longitudinal propagation was occurring, causing the APs in the contiguous chains to become bunched up. Transverse propagation was more erratic and labile in SMC compared to CMC. Transverse transmission of excitation did not require low-resistance connections between the chains, but instead depended on the value of R(ol2). The tighter the packing of the chains facilitated transverse propagation. BioMed Central 2004-03-03 /pmc/articles/PMC400751/ /pubmed/14998434 http://dx.doi.org/10.1186/1475-925X-3-5 Text en Copyright © 2004 Sperelakis and Kalloor; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research
Sperelakis, Nicholas
Kalloor, Bijoy
Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations
title Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations
title_full Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations
title_fullStr Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations
title_full_unstemmed Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations
title_short Transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in PSpice simulations
title_sort transverse propagation of action potentials between parallel chains of cardiac muscle and smooth muscle cells in pspice simulations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC400751/
https://www.ncbi.nlm.nih.gov/pubmed/14998434
http://dx.doi.org/10.1186/1475-925X-3-5
work_keys_str_mv AT sperelakisnicholas transversepropagationofactionpotentialsbetweenparallelchainsofcardiacmuscleandsmoothmusclecellsinpspicesimulations
AT kalloorbijoy transversepropagationofactionpotentialsbetweenparallelchainsofcardiacmuscleandsmoothmusclecellsinpspicesimulations