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Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells

Pulse electric field‐based (PEF) ablation is a technique whereby short high‐intensity electric fields inducing irreversible electroporation (IRE) are applied to various tissues. Here, we implemented a standardized in vitro model to compare the effects of biphasic symmetrical pulses (100 pulses, 1–10...

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Autores principales: Casciola, Maura, Keck, Devin, Feaster, Tromondae K., Blinova, Ksenia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612150/
https://www.ncbi.nlm.nih.gov/pubmed/36301726
http://dx.doi.org/10.14814/phy2.15493
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author Casciola, Maura
Keck, Devin
Feaster, Tromondae K.
Blinova, Ksenia
author_facet Casciola, Maura
Keck, Devin
Feaster, Tromondae K.
Blinova, Ksenia
author_sort Casciola, Maura
collection PubMed
description Pulse electric field‐based (PEF) ablation is a technique whereby short high‐intensity electric fields inducing irreversible electroporation (IRE) are applied to various tissues. Here, we implemented a standardized in vitro model to compare the effects of biphasic symmetrical pulses (100 pulses, 1–10 μs phase duration (d), 10–1000 Hz pulse repetition rate (f)) using two different human cellular models: human‐induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs) and human esophageal smooth muscle cells (hESMCs) cultured in monolayer format. We report the PEF‐induced irreversibly electroporated cell monolayer areas and the corresponding electric field thresholds (EFTs) for both cardiac and esophageal cultures. Our results suggest marked cell type specificity with EFT estimated to be 2–2.5 times lower in hiPSC‐CMs than in hESMCs when subjected to identical PEF treatments (e.g., 0.90 vs 1.85 kV/cm for the treatment of 100 pulses with d = 5 μs, f = 10 Hz, and 0.65 vs 1.67 kV/cm for the treatment of 100 pulses with d = 10 μs, f = 10 Hz). PEF treatment can result in increased temperature around the stimulating electrodes and lead to unanticipated thermal tissue damage that is proportional to the peak temperature rise and to the duration of the PEF‐induced elevated temperatures. In our study, temperature increases ranged from less than 1°C to as high as 30°C, however, all temperature changes were transient and quickly returned to baseline and the highest observed ∆T returned to 50% of its maximum recorded temperature in tens of seconds.
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spelling pubmed-96121502022-10-28 Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells Casciola, Maura Keck, Devin Feaster, Tromondae K. Blinova, Ksenia Physiol Rep Original Articles Pulse electric field‐based (PEF) ablation is a technique whereby short high‐intensity electric fields inducing irreversible electroporation (IRE) are applied to various tissues. Here, we implemented a standardized in vitro model to compare the effects of biphasic symmetrical pulses (100 pulses, 1–10 μs phase duration (d), 10–1000 Hz pulse repetition rate (f)) using two different human cellular models: human‐induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs) and human esophageal smooth muscle cells (hESMCs) cultured in monolayer format. We report the PEF‐induced irreversibly electroporated cell monolayer areas and the corresponding electric field thresholds (EFTs) for both cardiac and esophageal cultures. Our results suggest marked cell type specificity with EFT estimated to be 2–2.5 times lower in hiPSC‐CMs than in hESMCs when subjected to identical PEF treatments (e.g., 0.90 vs 1.85 kV/cm for the treatment of 100 pulses with d = 5 μs, f = 10 Hz, and 0.65 vs 1.67 kV/cm for the treatment of 100 pulses with d = 10 μs, f = 10 Hz). PEF treatment can result in increased temperature around the stimulating electrodes and lead to unanticipated thermal tissue damage that is proportional to the peak temperature rise and to the duration of the PEF‐induced elevated temperatures. In our study, temperature increases ranged from less than 1°C to as high as 30°C, however, all temperature changes were transient and quickly returned to baseline and the highest observed ∆T returned to 50% of its maximum recorded temperature in tens of seconds. John Wiley and Sons Inc. 2022-10-27 /pmc/articles/PMC9612150/ /pubmed/36301726 http://dx.doi.org/10.14814/phy2.15493 Text en Published 2022. This article is a U.S. Government work and is in the public domain in the USA. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Casciola, Maura
Keck, Devin
Feaster, Tromondae K.
Blinova, Ksenia
Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
title Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
title_full Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
title_fullStr Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
title_full_unstemmed Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
title_short Human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
title_sort human cardiomyocytes are more susceptible to irreversible electroporation by pulsed electric field than human esophageal cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612150/
https://www.ncbi.nlm.nih.gov/pubmed/36301726
http://dx.doi.org/10.14814/phy2.15493
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