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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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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. |
format | Online Article Text |
id | pubmed-3528752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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