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Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability

It is hypothesized that high frequency components of nanosecond pulsed electric fields (nsPEFs), determined by transient pulse features, are important for maximizing electric field interactions with intracellular structures. For monopolar square wave pulses, these transient features are determined b...

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Autores principales: Beebe, Stephen J., Chen, Yeong-Jer, Sain, Nova M., Schoenbach, Karl H., Xiao, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528752/
https://www.ncbi.nlm.nih.gov/pubmed/23284682
http://dx.doi.org/10.1371/journal.pone.0051349
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author Beebe, Stephen J.
Chen, Yeong-Jer
Sain, Nova M.
Schoenbach, Karl H.
Xiao, Shu
author_facet Beebe, Stephen J.
Chen, Yeong-Jer
Sain, Nova M.
Schoenbach, Karl H.
Xiao, Shu
author_sort Beebe, Stephen J.
collection PubMed
description It is hypothesized that high frequency components of nanosecond pulsed electric fields (nsPEFs), determined by transient pulse features, are important for maximizing electric field interactions with intracellular structures. For monopolar square wave pulses, these transient features are determined by the rapid rise and fall of the pulsed electric fields. To determine effects on mitochondria membranes and plasma membranes, N1-S1 hepatocellular carcinoma cells were exposed to single 600 ns pulses with varying electric fields (0–80 kV/cm) and short (15 ns) or long (150 ns) rise and fall times. Plasma membrane effects were evaluated using Fluo-4 to determine calcium influx, the only measurable source of increases in intracellular calcium. Mitochondria membrane effects were evaluated using tetramethylrhodamine ethyl ester (TMRE) to determine mitochondria membrane potentials (ΔΨm). Single pulses with short rise and fall times caused electric field-dependent increases in calcium influx, dissipation of ΔΨm and cell death. Pulses with long rise and fall times exhibited electric field-dependent increases in calcium influx, but diminished effects on dissipation of ΔΨm and viability. Results indicate that high frequency components have significant differential impact on mitochondria membranes, which determines cell death, but lesser variances on plasma membranes, which allows calcium influxes, a primary determinant for dissipation of ΔΨm and cell death.
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spelling pubmed-35287522013-01-02 Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability Beebe, Stephen J. Chen, Yeong-Jer Sain, Nova M. Schoenbach, Karl H. Xiao, Shu PLoS One Research Article It is hypothesized that high frequency components of nanosecond pulsed electric fields (nsPEFs), determined by transient pulse features, are important for maximizing electric field interactions with intracellular structures. For monopolar square wave pulses, these transient features are determined by the rapid rise and fall of the pulsed electric fields. To determine effects on mitochondria membranes and plasma membranes, N1-S1 hepatocellular carcinoma cells were exposed to single 600 ns pulses with varying electric fields (0–80 kV/cm) and short (15 ns) or long (150 ns) rise and fall times. Plasma membrane effects were evaluated using Fluo-4 to determine calcium influx, the only measurable source of increases in intracellular calcium. Mitochondria membrane effects were evaluated using tetramethylrhodamine ethyl ester (TMRE) to determine mitochondria membrane potentials (ΔΨm). Single pulses with short rise and fall times caused electric field-dependent increases in calcium influx, dissipation of ΔΨm and cell death. Pulses with long rise and fall times exhibited electric field-dependent increases in calcium influx, but diminished effects on dissipation of ΔΨm and viability. Results indicate that high frequency components have significant differential impact on mitochondria membranes, which determines cell death, but lesser variances on plasma membranes, which allows calcium influxes, a primary determinant for dissipation of ΔΨm and cell death. Public Library of Science 2012-12-21 /pmc/articles/PMC3528752/ /pubmed/23284682 http://dx.doi.org/10.1371/journal.pone.0051349 Text en © 2012 Beebe et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Beebe, Stephen J.
Chen, Yeong-Jer
Sain, Nova M.
Schoenbach, Karl H.
Xiao, Shu
Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability
title Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability
title_full Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability
title_fullStr Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability
title_full_unstemmed Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability
title_short Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability
title_sort transient features in nanosecond pulsed electric fields differentially modulate mitochondria and viability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528752/
https://www.ncbi.nlm.nih.gov/pubmed/23284682
http://dx.doi.org/10.1371/journal.pone.0051349
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