Stein Wolfgang, Städele Carola, Andras Peter
Institute of Neurobiology, Ulm University.
J Vis Exp. 2011 Mar 23(49):2567. doi: 10.3791/2567.
Voltage-sensitive dye imaging of neurons is a key methodology for the understanding of how neuronal networks are organised and how the simultaneous activity of participating neurons leads to the emergence of the integral functionality of the network. Here we present the methodology of application of this technique to identified pattern generating neurons in the crab stomatogastric ganglion. We demonstrate the loading of these neurons with the fluorescent voltage-sensitive dye Di-8-ANEPPQ and we show how to image the activity of dye loaded neurons using the MiCAM02 high speed and high resolution CCD camera imaging system. We demonstrate the analysis of the recorded imaging data using the BVAna imaging software associated with the MiCAM02 imaging system. The simultaneous voltage-sensitive dye imaging of the detailed activity of multiple neurons in the crab stomatogastric ganglion applied together with traditional electrophysiology techniques (intracellular and extracellular recordings) opens radically new opportunities for the understanding of how central pattern generator neural networks work.
神经元的电压敏感染料成像技术是理解神经元网络如何组织以及参与其中的神经元的同步活动如何导致网络整体功能出现的关键方法。在此,我们介绍将该技术应用于蟹类口胃神经节中已识别的模式生成神经元的方法。我们展示了如何用荧光电压敏感染料Di-8-ANEPPQ加载这些神经元,并展示了如何使用MiCAM02高速高分辨率CCD相机成像系统对加载了染料的神经元的活动进行成像。我们演示了使用与MiCAM02成像系统相关联的BVAna成像软件对记录的成像数据进行分析。将蟹类口胃神经节中多个神经元的详细活动的同步电压敏感染料成像与传统电生理技术(细胞内和细胞外记录)结合使用,为理解中枢模式发生器神经网络的工作方式带来了全新的机遇。