Department of Biology, Loyola University Chicago, Chicago, USA.
Department of Biology, Loyola University Chicago, Chicago, USA.
J Neurosci Methods. 2022 Jan 1;365:109401. doi: 10.1016/j.jneumeth.2021.109401. Epub 2021 Oct 30.
Extracellular recording of nerve activities using suction electrodes is an easy yet powerful tool in characterizing neural activities in physiology and pathological conditions. The key factors that determine the quality of suction electrode recordings have not been fully investigated. New Methods: Here, we proposed a biophysical model to study the mechanisms underlying suction technology for axon recording. The model focuses on the interpretation of the recorded single neuron activity based on the location of the electrode, the integrity of the recorded tissue, and the tightness of the suction. To directly test these model predictions, we applied two channel recordings from the nerves in Aplysia californica, and analyzed the shape of the extracellularly recorded single neuron activity under various conditions.
We found that both the recording site and the integrity of the neural tissue impact the shape of the action potentials traveling along the axon. In practice, the tightness of the suction is the key parameter for high-quality recordings using a suction electrode. Comparison with Existing Methods: Experimental protocols that can improve precise positioning of the electrode tip to the target nerve, avoid tissue damage, enhance suction force, and maintain tightness are essential for high-quality suction recording from axons. Current methods have not emphasized on achieving and maintaining of the suction pressure during experimentation, and have sometimes ignored the impact of suction electrode position or tissue damage to the quality of the recorded neural signal.
A combined theoretical analysis and experimental approach is essential in improving neural recording technology. The work provides theoretical and practical guidelines to improve suction technology. This work also provides valuable insights to the improvement of several other extracellular recording technology in laboratory research or clinical settings.
使用吸管电极进行神经活动的细胞外记录是一种在生理和病理条件下描述神经活动的简单而强大的工具。决定吸管电极记录质量的关键因素尚未得到充分研究。
在这里,我们提出了一个生物物理模型来研究用于轴突记录的吸管技术的机制。该模型侧重于根据电极位置、记录组织的完整性和吸力的紧密度来解释记录的单个神经元活动。为了直接测试这些模型预测,我们从加利福尼亚海兔的神经中应用了双通道记录,并分析了在各种条件下记录的单个神经元活动的形状。
我们发现,记录部位和神经组织的完整性都影响沿着轴突传播的动作电位的形状。在实践中,吸管的紧密度是使用吸管电极进行高质量记录的关键参数。
能够提高电极尖端到目标神经的精确定位、避免组织损伤、增强吸力和保持紧密度的实验方案对于从轴突进行高质量的吸管记录至关重要。目前的方法没有强调在实验过程中实现和维持吸力压力,并且有时忽略了吸管电极位置或组织损伤对记录的神经信号质量的影响。
理论分析和实验方法的结合对于改进神经记录技术至关重要。这项工作为改进吸管技术提供了理论和实践指导。这项工作还为实验室研究或临床环境中几种其他细胞外记录技术的改进提供了有价值的见解。