局部离子导入在长期突触抑制药理诱导中的应用。

IF 1 Q3 BIOLOGY
Borys Olifirov, Oleksandra Fedchenko, Alexandr Dovgan, Daria Babets, Volodymyr Krotov, Volodymyr Cherkas, Pavel Belan
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引用次数: 0

摘要

长期抑制(LTD)是突触可塑性的一种关键形式,通常通过调节Ca2+通过NMDA受体进入诱导,并通过长时间(长达数百秒)低频突触前刺激或NMDA受体激动剂的大量应用来实现。电生理方法对LTD感应需要专门的设备,而浴的应用限制了生产率,因为每个样本只能记录一个神经元。在这里,我们提出了一个简单而有效的方案,用于在原代培养的神经元中建立LTD的药理模型。该方法依赖于NMDA的高度局部离子化应用,在单个细胞中诱导LTD,提高实验通量。我们分析了离子电泳药物递送的时空模式,并展示了该技术如何与电生理和活细胞成像方法相结合,以研究突触强度和神经元Ca2+传感器蛋白Ca2+依赖信号的ltd相关变化。•使用离子吸附NMDA应用在原代培养神经元中容易、快速、可靠地诱导LTD。•适用于任何离子水溶性化合物的应用,并与同时多色荧光成像和电生理记录兼容。•该方案使单个神经元的药理学靶向,大大增加了实验吞吐量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Local Iontophoretic Application for Pharmacological Induction of Long-Term Synaptic Depression.

Long-term depression (LTD), a key form of synaptic plasticity, is typically induced through regulated Ca2+ entry via NMDA receptors and achieved by prolonged (up to hundreds of seconds) low-frequency presynaptic stimulation or bath application of NMDA receptor agonists. Electrophysiological approach to LTD induction requires specialized equipment, while bath applications limit productivity, as only one neuron per sample may be recorded. Here, we present a simple and effective protocol for pharmacological modeling of LTD in primary cultured neurons. This approach relies on highly localized iontophoretic application of NMDA, which induces LTD in individual cells, enhancing experimental throughput. We have analyzed spatio-temporal patterns of iontophoretic drug delivery and demonstrated how this technique may be combined with electrophysiological and live-cell imaging approaches to investigate LTD-related changes in synaptic strength and Ca2+-dependent signaling of neuronal Ca2+ sensor proteins. Key features • Easy, fast, and reliable induction of LTD in primary cultured neurons using iontophoretic NMDA application. • Suitable for the application of any ionic water-soluble compound and compatible with simultaneous multicolor fluorescence imaging and electrophysiological recording. • This protocol enables pharmacological targeting of individual neurons, substantially increasing experimental throughput.

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CiteScore
1.50
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