Abstract

BackgroundExtracellular recording represents a crucial electrophysiological technique in neuroscience for studying the activity of single neurons and neuronal populations. The electrodes capture voltage traces that, with the help of analytical tools, reveal action potentials (‘spikes’) as well as local field potentials. The process of spike sorting is used for the extraction of action potentials generated by individual neurons. Until recently, spike sorting was performed with manual techniques, which are laborious and unreliable due to inherent operator bias. As neuroscientists add multiple electrodes to their probes, the high-density devices can record hundreds to thousands of neurons simultaneously, making the manual spike sorting process increasingly difficult. The advent of automated spike sorting software has offered a compelling solution to this issue and, in this study, we present a simple-to-execute framework for running an automated spike sorter.MethodsTetrode recordings of freely-moving mice are obtained from the CA1 region of the hippocampus as they navigate a linear track. Tetrode recordings are also acquired from the prelimbic cortex, a region of the medial prefrontal cortex, while the mice are tested in a T maze. All animals are implanted with custom-designed, 3D-printed microdrives that carry 16 electrodes, which are bundled in a 4-tetrode geometry.ResultsWe provide an overview of a framework for analyzing single-unit data in which we have concatenated the acquisition system (Cheetah, Neuralynx) with analytical software (MATLAB) and an automated spike sorting pipeline (MountainSort). We give precise instructions on how to implement the different steps of the framework, as well as explanations of our design logic. We validate this framework by comparing manually-sorted spikes against automatically-sorted spikes, using neural recordings of the hippocampus and prelimbic cortex in freely-moving mice.ConclusionsWe have efficiently integrated the MountainSort spike sorter with Neuralynx-acquired neural recordings. Our framework is easy to implement and provides a high-throughput solution. We predict that within the broad field of bioelectronic medicine, those teams that incorporate high-density neural recording devices to their armamentarium might find our framework quite valuable as they expand their analytical footprint.

Highlights

  • Extracellular recording represents a crucial electrophysiological technique in neuroscience for studying the activity of single neurons and neuronal populations

  • A central goal of this work is to provide a roadmap for analysis of single-unit data, with a focus on how we have concatenated the Cheetah system with MATLAB and the automated spike sorting technology, MountainSort

  • The continuous datastream is saved in the files named CSC1.ncs up to CSC16.ncs (Neuralynx continuously sampled), which comprise the voltage at every timestamp for each separate channel

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Summary

Introduction

Extracellular recording represents a crucial electrophysiological technique in neuroscience for studying the activity of single neurons and neuronal populations. In vivo electrophysiological techniques with extracellular electrodes that measure action potentials (‘spikes’) and subthreshold oscillations have been used to record activity from the brain of several mammalian species and have generated a tremendous amount of information (Cacucci et al, 2008; O'Keefe and Dostrovsky, 1971; O’Keefe and Nadel, 1976; Kunz, et al, 2021). After obtaining a tetrode recording, spike sorting is a mandatory step for the isolation of neuronal units. This process begins by applying a band-pass filter followed by a voltage threshold to detect all events which fall into the frequency and voltage ranges containing neural spikes. Clusters or events which are either poorly isolated or likely to correspond to background noise are removed from further analysis

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