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局部离子电渗疗法用于药理学诱导长期突触抑制

Local Iontophoretic Application for Pharmacological Induction of Long-Term Synaptic Depression.

作者信息

Olifirov Borys, Fedchenko Oleksandra, Dovgan Alexandr, Babets Daria, Krotov Volodymyr, Cherkas Volodymyr, Belan Pavel

机构信息

Department of Molecular Biophysics, Bogomoletz Institute of Physiology, NAS of Ukraine, Kyiv, Ukraine.

Laboratory of Molecular Assays and Imaging, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.

出版信息

Bio Protoc. 2025 Jun 5;15(11):e5338. doi: 10.21769/BioProtoc.5338.

DOI:10.21769/BioProtoc.5338
PMID:40511409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12152103/
Abstract

Long-term depression (LTD), a key form of synaptic plasticity, is typically induced through regulated Ca 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 Ca-dependent signaling of neuronal Ca 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.

摘要

长时程抑制(LTD)是突触可塑性的一种关键形式,通常通过NMDA受体介导的钙离子内流来诱导,并通过长时间(长达数百秒)的低频突触前刺激或浴式应用NMDA受体激动剂来实现。诱导LTD的电生理方法需要专门的设备,而浴式应用则限制了实验效率,因为每个样本只能记录一个神经元。在此,我们介绍一种在原代培养神经元中对LTD进行药理学模拟的简单有效方案。该方法依赖于NMDA的高度局部离子电渗应用,可在单个细胞中诱导LTD,提高实验通量。我们分析了离子电渗给药的时空模式,并展示了该技术如何与电生理和活细胞成像方法相结合,以研究与LTD相关的突触强度变化以及神经元钙传感器蛋白的钙依赖性信号传导。关键特性 • 使用离子电渗应用NMDA在原代培养神经元中轻松、快速且可靠地诱导LTD。 • 适用于任何离子水溶性化合物的应用,并与同步多色荧光成像和电生理记录兼容。 • 该方案能够对单个神经元进行药理学靶向,大幅提高实验通量。

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