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Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes
AIMS: Cardiac electrophysiological heterogeneity includes: (i) regional differences in action potential (AP) waveform, (ii) AP waveform differences in cells isolated from a single region, (iii) variability of the contribution of individual ion currents in cells with similar AP durations (APDs). The...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732512/ https://www.ncbi.nlm.nih.gov/pubmed/35020837 http://dx.doi.org/10.1093/cvr/cvab375 |
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author | Lachaud, Quentin Aziz, Muhamad Hifzhudin Noor Burton, Francis L Macquaide, Niall Myles, Rachel C Simitev, Radostin D Smith, Godfrey L |
author_facet | Lachaud, Quentin Aziz, Muhamad Hifzhudin Noor Burton, Francis L Macquaide, Niall Myles, Rachel C Simitev, Radostin D Smith, Godfrey L |
author_sort | Lachaud, Quentin |
collection | PubMed |
description | AIMS: Cardiac electrophysiological heterogeneity includes: (i) regional differences in action potential (AP) waveform, (ii) AP waveform differences in cells isolated from a single region, (iii) variability of the contribution of individual ion currents in cells with similar AP durations (APDs). The aim of this study is to assess intra-regional AP waveform differences, to quantify the contribution of specific ion channels to the APD via drug responses and to generate a population of mathematical models to investigate the mechanisms underlying heterogeneity in rabbit ventricular cells. METHODS AND RESULTS: APD in ∼50 isolated cells from subregions of the LV free wall of rabbit hearts were measured using a voltage-sensitive dye. When stimulated at 2 Hz, average APD(90) value in cells from the basal epicardial region was 254 ± 25 ms (mean ± standard deviation) in 17 hearts with a mean interquartile range (IQR) of 53 ± 17 ms. Endo-epicardial and apical-basal APD(90) differences accounted for ∼10% of the IQR value. Highly variable changes in APD occurred after IK(r) or ICa(L) block that included a sub-population of cells (HR) with an exaggerated (hyper) response to IK(r) inhibition. A set of 4471 AP models matching the experimental APD(90) distribution was generated from a larger population of models created by random variation of the maximum conductances (G(max)) of 8 key ion channels/exchangers/pumps. This set reproduced the pattern of cell-specific responses to ICa(L) and IK(r) block, including the HR sub-population. The models exhibited a wide range of G(max) values with constrained relationships linking ICa(L) with IK(r), ICl, INCX, and INaK. CONCLUSION: Modelling the measured range of inter-cell APDs required a larger range of key G(max) values indicating that ventricular tissue has considerable inter-cell variation in channel/pump/exchanger activity. AP morphology is retained by relationships linking specific ionic conductances. These interrelationships are necessary for stable repolarization despite large inter-cell variation of individual conductances and this explains the variable sensitivity to ion channel block. |
format | Online Article Text |
id | pubmed-9732512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97325122022-12-13 Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes Lachaud, Quentin Aziz, Muhamad Hifzhudin Noor Burton, Francis L Macquaide, Niall Myles, Rachel C Simitev, Radostin D Smith, Godfrey L Cardiovasc Res Original Article AIMS: Cardiac electrophysiological heterogeneity includes: (i) regional differences in action potential (AP) waveform, (ii) AP waveform differences in cells isolated from a single region, (iii) variability of the contribution of individual ion currents in cells with similar AP durations (APDs). The aim of this study is to assess intra-regional AP waveform differences, to quantify the contribution of specific ion channels to the APD via drug responses and to generate a population of mathematical models to investigate the mechanisms underlying heterogeneity in rabbit ventricular cells. METHODS AND RESULTS: APD in ∼50 isolated cells from subregions of the LV free wall of rabbit hearts were measured using a voltage-sensitive dye. When stimulated at 2 Hz, average APD(90) value in cells from the basal epicardial region was 254 ± 25 ms (mean ± standard deviation) in 17 hearts with a mean interquartile range (IQR) of 53 ± 17 ms. Endo-epicardial and apical-basal APD(90) differences accounted for ∼10% of the IQR value. Highly variable changes in APD occurred after IK(r) or ICa(L) block that included a sub-population of cells (HR) with an exaggerated (hyper) response to IK(r) inhibition. A set of 4471 AP models matching the experimental APD(90) distribution was generated from a larger population of models created by random variation of the maximum conductances (G(max)) of 8 key ion channels/exchangers/pumps. This set reproduced the pattern of cell-specific responses to ICa(L) and IK(r) block, including the HR sub-population. The models exhibited a wide range of G(max) values with constrained relationships linking ICa(L) with IK(r), ICl, INCX, and INaK. CONCLUSION: Modelling the measured range of inter-cell APDs required a larger range of key G(max) values indicating that ventricular tissue has considerable inter-cell variation in channel/pump/exchanger activity. AP morphology is retained by relationships linking specific ionic conductances. These interrelationships are necessary for stable repolarization despite large inter-cell variation of individual conductances and this explains the variable sensitivity to ion channel block. Oxford University Press 2022-01-10 /pmc/articles/PMC9732512/ /pubmed/35020837 http://dx.doi.org/10.1093/cvr/cvab375 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lachaud, Quentin Aziz, Muhamad Hifzhudin Noor Burton, Francis L Macquaide, Niall Myles, Rachel C Simitev, Radostin D Smith, Godfrey L Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
title | Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
title_full | Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
title_fullStr | Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
title_full_unstemmed | Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
title_short | Electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
title_sort | electrophysiological heterogeneity in large populations of rabbit ventricular cardiomyocytes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732512/ https://www.ncbi.nlm.nih.gov/pubmed/35020837 http://dx.doi.org/10.1093/cvr/cvab375 |
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