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Chunk #44 — Understanding MEA signals — What do microelectrodes detect?

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Revealing neuronal function through microelectrode array recordings.
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An AP is a biophysical event that occurs once the neuron's transmembrane potential reaches a threshold due to stimuli or other inputs (e.g., synapses, gap junctions). On the other hand, we consider a “spike” to be the signal from a putative AP. For extracellular recordings, spikes are commonly identified as voltage signals that exceed a threshold. During an AP, the initial rapid Na+ ion influx creates a sink and results in a large negative spike in the EAP. Thereafter, the slow K+ efflux produces a source resulting in a small positive spike. In contrast, IAP first shows a positive spike and later a negative volley. EAPs are usually around tens to hundreds of microvolts in amplitude and <2 ms in duration while IAPs are at tens of millivolts and around the same duration as EAPs (Buzsáki et al., 2012). If IAPs can only be detected by direct access inside the neuron, e.g., patch-clamp, EAPs can be identified when electrodes are placed at the vicinity (~100 μm) of the spike origin (Henze et al., 2000; Egert et al., 2002), usually at the perisomatic area, i.e., around the soma or near the axon initial segment.