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本文引用的文献

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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。
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Multi-electrode array technologies for neuroscience and cardiology.多电极阵列技术在神经科学和心脏病学中的应用。
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Fiji: an open-source platform for biological-image analysis.斐济:一个用于生物影像分析的开源平台。
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Optically monitoring voltage in neurons by photo-induced electron transfer through molecular wires.通过分子导线的光诱导电子转移来光学监测神经元中的电压。
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Induced transmembrane voltage and its correlation with electroporation-mediated molecular transport.诱导跨膜电压及其与电穿孔介导的分子传递的相关性。
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Plasma membrane permeabilization by trains of ultrashort electric pulses.通过超短电脉冲串使质膜穿孔。
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Measuring the induced membrane voltage with Di-8-ANEPPS.用Di-8-ANEPPS测量诱导膜电压。
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Two-dimensional nanosecond electric field mapping based on cell electropermeabilization.基于细胞电通透化的二维纳秒电场映射
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Electrophysiology in the age of light.光时代的电生理学。
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Submillisecond optical reporting of membrane potential in situ using a neuronal tracer dye.使用神经元示踪染料对原位膜电位进行亚毫秒级光学报告。
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可视化膜电位的动态亚微秒变化。

Visualization of Dynamic Sub-microsecond Changes in Membrane Potential.

机构信息

Bioeffects Division, Air Force Research Laboratory, JBSA Fort Sam Houston, Texas.

Bioeffects Division, Air Force Research Laboratory, JBSA Fort Sam Houston, Texas.

出版信息

Biophys J. 2019 Jan 8;116(1):120-126. doi: 10.1016/j.bpj.2018.11.3129. Epub 2018 Dec 1.

DOI:10.1016/j.bpj.2018.11.3129
PMID:30579565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6342736/
Abstract

Direct observation of rapid membrane potential changes is critical to understand how complex neurological systems function. This knowledge is especially important when stimulation is achieved through an external stimulus meant to mimic a naturally occurring process. To enable exploration of this dynamic space, we developed an all-optical method for observing rapid changes in membrane potential at temporal resolutions of ∼25 ns. By applying a single 600-ns electric pulse, we observed sub-microsecond, continuous membrane charging and discharging dynamics. Close agreement between the acquired results and an analytical membrane-charging model validates the utility of this technique. This tool will deepen our understanding of the role of membrane potential dynamics in the regulation of many biological and chemical processes within living systems.

摘要

直接观察快速的膜电位变化对于理解复杂的神经系统功能至关重要。当刺激是通过外部刺激来模拟自然发生的过程时,这种知识尤为重要。为了能够探索这个动态空间,我们开发了一种全光学方法,用于以约 25ns 的时间分辨率观察膜电位的快速变化。通过施加单个 600ns 的电脉冲,我们观察到亚微秒的连续膜充电和放电动力学。获得的结果与有效的分析膜充电模型之间的紧密一致验证了该技术的实用性。该工具将加深我们对膜电位动力学在调节活体内许多生物和化学过程中的作用的理解。