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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Neuronal excitation and permeabilization by 200-ns pulsed electric field: An optical membrane potential study with FluoVolt dye
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Neuronal excitation and permeabilization by 200-ns pulsed electric field: An optical membrane potential study with FluoVolt dye

机译:200-NS脉冲电场的神经元励磁和渗透性:用氟玻璃染料进行光学膜潜在研究

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摘要

Electric field pulses of nano- and picosecond duration are a novel modality for neurostimulation, activation of Ca2+ signaling, and tissue ablation. However it is not known how such brief pulses activate voltage-gated ion channels. We studied excitation and electroporation of hippocampal neurons by 200-ns pulsed electric field (nsPEF), by means of time-lapse imaging of the optical membrane potential (OMP) with FluoVolt dye. Electroporation abruptly shifted OMP to a more depolarized level, which was reached within <1 ms. The OMP recovery started rapidly (T = 8-12 ms) but gradually slowed down (to T> 10 s), so cells remained above the resting OMP level for at least 20-30 s. Activation of voltage-gated sodium channels (VGSC) enhanced the depolarizing effect of electroporation, resulting in an additional tetrodotoxin-sensitive OMP peak in 4-5 ms after nsPEF. Omitting Ca2+ in the extracellular solution did not reduce the depolarization, suggesting no contribution of voltage gated calcium channels (VGCC). In 40% of neurons, nsPEF triggered a single action potential (AP), with the median threshold of 3 kV/cm (range: 1.9-4 kV/cm); no APs could be evoked by stimuli below the electroporation threshold (1.5-1.9 kV/cm). VGSC opening could already be detected in 0.5 ms after nsPEF, which is too fast to be mediated by the depolarizing effect of electroporation. The overlap of electroporation and AP thresholds does not necessarily reflect the causal relation, but suggests a low potency of nsPEF, as compared to conventional electrostimulation, for VGSC activation and AP induction. (C) 2017 Elsevier B.V. All rights reserved.
机译:纳米和皮秒持续时间的电场脉冲是用于神经刺激,CA2 +信号传导的激活和组织消融的新型模态。然而,尚不知道这种短暂脉冲如何激活电压门控离子通道。我们通过用氟玻璃电位(OMP)的时间延迟成像来研究200-NS脉冲电场(NSPEF)的海马神经元的激发和电穿孔。电穿孔突然移位到更达极化的水平,其达到在<1ms内。 OMP恢复快速启动(T = 8-12毫秒),但逐渐减慢(t> 10 s),因此细胞仍然高于静止的OM水平至少20-30秒。电压门控钠通道(VGSC)的激活增强了电穿孔的去极化效果,从而在NPSPEF之后在4-5毫秒中得到另外的四曲毒素敏感的峰。省略细胞外溶液中的Ca2 +未降低去极化,表明电压门控钙通道(VGCC)没有贡献。在40%的神经元中,NPEF触发了单一动作电位(AP),中间阈值3 kV / cm(范围:1.9-4 kV / cm);可以通过低于电穿孔阈值(1.5-1.9kV / cm)的刺激唤起APS。在NPSP之后已经在0.5ms中检测到VGSC开口,这太快了通过电穿孔的去极化效果介导。电穿孔和AP阈值的重叠不一定反映因果关系,而是与传统的电动刺激相比,NPEF的低效力,用于VGSC激活和AP感应。 (c)2017 Elsevier B.v.保留所有权利。

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