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Next generation CANCAN focusing for remote stimulation by nanosecond electric pulses.下一代 CANCAN 聚焦用于纳秒电脉冲的远程刺激。
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本文引用的文献

1
Bipolar nanosecond electric pulses are less efficient at electropermeabilization and killing cells than monopolar pulses.双相纳秒电脉冲在细胞电穿孔和杀伤方面的效率不如单极脉冲。
Biochem Biophys Res Commun. 2014 Jan 10;443(2):568-73. doi: 10.1016/j.bbrc.2013.12.004. Epub 2013 Dec 8.
2
Molecular dynamics simulations of ion conductance in field-stabilized nanoscale lipid electropores.场稳定纳米级脂质电穿孔中离子电导的分子动力学模拟
J Phys Chem B. 2013 Oct 3;117(39):11633-40. doi: 10.1021/jp401722g. Epub 2013 Sep 19.
3
Two modes of cell death caused by exposure to nanosecond pulsed electric field.两种由纳秒级脉冲电场暴露引起的细胞死亡模式。
PLoS One. 2013 Jul 23;8(7):e70278. doi: 10.1371/journal.pone.0070278. Print 2013.
4
Recruitment of the intracellular Ca2+ by ultrashort electric stimuli: the impact of pulse duration.超短电刺激对细胞内 Ca2+的募集:脉宽的影响。
Cell Calcium. 2013 Sep;54(3):145-50. doi: 10.1016/j.ceca.2013.05.008. Epub 2013 Jun 15.
5
Activation of intracellular phosphoinositide signaling after a single 600 nanosecond electric pulse.单次 600 纳秒电脉冲后细胞内磷酸肌醇信号的激活。
Bioelectrochemistry. 2013 Dec;94:23-9. doi: 10.1016/j.bioelechem.2013.05.002. Epub 2013 May 20.
6
Electric field-driven water dipoles: nanoscale architecture of electroporation.电场驱动的水分子偶极子:电穿孔的纳米结构。
PLoS One. 2013 Apr 11;8(4):e61111. doi: 10.1371/journal.pone.0061111. Print 2013.
7
Facilitation of electroporative drug uptake and cell killing by electrosensitization.电增敏作用促进电穿孔药物摄取和细胞杀伤。
J Cell Mol Med. 2013 Jan;17(1):154-9. doi: 10.1111/j.1582-4934.2012.01658.x. Epub 2013 Jan 11.
8
Transient features in nanosecond pulsed electric fields differentially modulate mitochondria and viability.纳秒级脉冲电场中的瞬态特征可差异调节线粒体和活力。
PLoS One. 2012;7(12):e51349. doi: 10.1371/journal.pone.0051349. Epub 2012 Dec 21.
9
Primary pathways of intracellular Ca(2+) mobilization by nanosecond pulsed electric field.纳秒级脉冲电场引起细胞内钙离子动员的主要途径
Biochim Biophys Acta. 2013 Mar;1828(3):981-9. doi: 10.1016/j.bbamem.2012.11.032. Epub 2012 Dec 5.
10
Oxidative effects of nanosecond pulsed electric field exposure in cells and cell-free media.纳秒级脉冲电场暴露对细胞和无细胞培养基中细胞的氧化效应。
Arch Biochem Biophys. 2012 Nov 1;527(1):55-64. doi: 10.1016/j.abb.2012.08.004. Epub 2012 Aug 15.

通过反转刺激极性来消除细胞对纳米电穿孔的反应。

Cancellation of cellular responses to nanoelectroporation by reversing the stimulus polarity.

作者信息

Pakhomov Andrei G, Semenov Iurii, Xiao Shu, Pakhomova Olga N, Gregory Betsy, Schoenbach Karl H, Ullery Jody C, Beier Hope T, Rajulapati Sambasiva R, Ibey Bennett L

机构信息

Frank Reidy Research Center for Bioelectrics, Old Dominion University, 4211 Monarch Way, Suite 300, Norfolk, VA, 23508, USA,

出版信息

Cell Mol Life Sci. 2014 Nov;71(22):4431-41. doi: 10.1007/s00018-014-1626-z. Epub 2014 Apr 21.

DOI:10.1007/s00018-014-1626-z
PMID:24748074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4205218/
Abstract

Nanoelectroporation of biomembranes is an effect of high-voltage, nanosecond-duration electric pulses (nsEP). It occurs both in the plasma membrane and inside the cell, and nanoporated membranes are distinguished by ion-selective and potential-sensitive permeability. Here we report a novel phenomenon of bioeffects cancellation that puts nsEP cardinally apart from the conventional electroporation and electrostimulation by milli- and microsecond pulses. We compared the effects of 60- and 300-ns monopolar, nearly rectangular nsEP on intracellular Ca(2+) mobilization and cell survival with those of bipolar 60 + 60 and 300 + 300 ns pulses. For diverse endpoints, exposure conditions, pulse numbers (1-60), and amplitudes (15-60 kV/cm), the addition of the second phase cancelled the effects of the first phase. The overall effect of bipolar pulses was profoundly reduced, despite delivering twofold more energy. Cancellation also took place when two phases were separated into two independent nsEP of opposite polarities; it gradually tapered out as the interval between two nsEP increased, but was still present even at a 10-µs interval. The phenomenon of cancellation is unique for nsEP and has not been predicted by the equivalent circuit, transport lattice, and molecular dynamics models of electroporation. The existing paradigms of membrane permeabilization by nsEP will need to be modified. Here we discuss the possible involvement of the assisted membrane discharge, two-step oxidation of membrane phospholipids, and reverse transmembrane ion transport mechanisms. Cancellation impacts nsEP applications in cancer therapy, electrostimulation, and biotechnology, and provides new insights into effects of more complex waveforms, including pulsed electromagnetic emissions.

摘要

生物膜的纳米电穿孔是高压、纳秒持续时间电脉冲(nsEP)的一种效应。它发生在质膜和细胞内部,纳米穿孔膜的特点是具有离子选择性和电位敏感性通透性。在此,我们报告了一种生物效应消除的新现象,这使得纳秒电脉冲与传统的毫秒和微秒脉冲电穿孔及电刺激在本质上有所不同。我们比较了60纳秒和300纳秒单极、近似矩形的纳秒电脉冲与双极60 + 60纳秒和300 + 300纳秒脉冲对细胞内钙离子动员和细胞存活的影响。对于不同的终点指标、暴露条件、脉冲数(1 - 60)和幅度(15 - 60 kV/cm),添加第二阶段会消除第一阶段的效应。尽管双极脉冲输送的能量增加了一倍,但其总体效应却大幅降低。当两个阶段被分离为两个极性相反的独立纳秒电脉冲时,也会发生消除现象;随着两个纳秒电脉冲之间的间隔增加,这种现象逐渐减弱,但即使在10微秒的间隔时仍然存在。消除现象是纳秒电脉冲所特有的,电穿孔的等效电路、传输晶格和分子动力学模型均未预测到这一点。现有的纳秒电脉冲使膜通透性增加的范式需要修改。在此,我们讨论了辅助膜放电、膜磷脂的两步氧化以及反向跨膜离子转运机制可能的参与情况。消除现象影响纳秒电脉冲在癌症治疗、电刺激和生物技术中的应用,并为包括脉冲电磁辐射在内的更复杂波形的效应提供了新的见解。