Document Type
Article
Publication Date
2012
Publication Title
PloS One
Volume
7
Issue
12
Pages
e51349
DOI
10.1371/journal.pone.0051349
Abstract
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 (DeltaPsim). Single pulses with short rise and fall times caused electric field-dependent increases in calcium influx, dissipation of DeltaPsim and cell death. Pulses with long rise and fall times exhibited electric field-dependent increases in calcium influx, but diminished effects on dissipation of DeltaPsim 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 DeltaPsim and cell death.
Original Publication Citation
Beebe, S.J., Chen, Y.J., Sain, N.M., Schoenbach, K.H., & Xiao, S. (2012). Transient features in nanosecond pulsed electric fields differentially modulate mitochondria and viability. PLoS One, 7(12), e51349. doi: 10.1371/journal.pone.0051349
Repository Citation
Beebe, Stephen J.; Chen, Yeong-Jer; Sain, Nova M.; Schoenbach, Karl H.; and Xiao, Shu, "Transient Features in Nanosecond Pulsed Electric Fields Differentially Modulate Mitochondria and Viability" (2012). Bioelectrics Publications. 22.
https://digitalcommons.odu.edu/bioelectrics_pubs/22