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Adaptation of Microelectrode Array Technology for the Study of Anesthesia-induced Neurotoxicity in the Intact Piglet Brain
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Published on: May 12, 2018

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Antioxidant Coated Microelectrode Arrays: Effects on Putative Inhibitory and Excitatory Neurons

Brandon S Sturgill, Madison S Jiang, Eleanor N Jeakle

    Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference
    |March 5, 2025
    PubMed

    Abstract:

    Intracortical microelectrode arrays (MEAs) are used to record neural activity in vivo at single-cell resolution for both neuroscience studies and for engineering restorative devices such as brain-computer interfaces (BCIs). The recording performance of these devices are known to degrade over weeks to months after implantation due, in part, to neuroinflammation and oxidative stress. Characterizing and mitigating the degradation of recording performance is of particular interest for chronic applications. Literature suggests that inhibitory neurons may be more susceptible to oxidative stress than excitatory neurons. In this study, we classify recorded neural signals as either putative inhibitory or excitatory based on their waveform characteristics and aim to identify if one preferentially benefits from the use of a Mn(III)tetrakis94-benzoic acid)porphyrin (MnTBAP) coating to reduce reactive oxygen species, which we have previously demonstrated improves chronic neural recordings. In this study, we found that the MnTBAP coating affects these two classes of neurons differently, depending on the cortical depth. The MnTBAP coating improves the number of putative inhibitory signals recorded on the middle electrode sites (L5) and putative excitatory units on the superficial (L2/3 & L4) electrode sites. Our results suggest that decreases in recording performance may be influenced by both cortical depth and neuronal cell type. Furthermore, we show that the benefits of a MnTBAP coating to chronic neural recordings differ between putative inhibitory and excitatory neurons with a depth dependence.

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