4.6 Article

Flexible microelectrode array for interfacing with the surface of neural ganglia

Journal

JOURNAL OF NEURAL ENGINEERING
Volume 15, Issue 3, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.1088/1741-2552/aab55f

Keywords

microelectrode; DRG; dorsal root ganglia; feline; polyimide; source localization; Aplysia

Funding

  1. Craig H Neilsen Foundation [314980]
  2. National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health [U18EB021760]
  3. Michigan Institute for Clinical and Health Research - National Center for Advancing Translational Studies of the National Institutes of Health [UL1TR000433, UL1TR002240]
  4. Michigan Brain Initiative Working Group (MiBrain)

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Objective. The dorsal root ganglia (DRG) are promising nerve structures for sensory neural interfaces because they provide centralized access to primary afferent cell bodies and spinal reflex circuitry. In order to harness this potential, new electrode technologies are needed which take advantage of the unique properties of DRG, specifically the high density of neural cell bodies at the dorsal surface. Here we report initial in vivo results from the development of a flexible non-penetrating polyimide electrode array interfacing with the surface of ganglia. Approach. Multiple layouts of a 64-channel iridium electrode (420 mu m(2)) array were tested, with pitch as small as 25 mu m. The buccal ganglia of invertebrate sea slug Aplysia californica were used to develop handling and recording techniques with ganglionic surface electrode arrays (GSEAs). We also demonstrated the GSEA's capability to record single-and multi-unit activity from feline lumbosacral DRG related to a variety of sensory inputs, including cutaneous brushing, joint flexion, and bladder pressure. Main results. We recorded action potentials from a variety of Aplysia neurons activated by nerve stimulation, and units were observed firing simultaneously on closely spaced electrode sites. We also recorded single-and multi-unit activity associated with sensory inputs from feline DRG. We utilized spatial oversampling of action potentials on closely-spaced electrode sites to estimate the location of neural sources at between 25 mu m and 107 mu m below the DRG surface. We also used the high spatial sampling to demonstrate a possible spatial sensory map of one feline's DRG. We obtained activation of sensory fibers with low-amplitude stimulation through individual or groups of GSEA electrode sites. Significance. Overall, the GSEA has been shown to provide a variety of information types from ganglia neurons and to have significant potential as a tool for neural mapping and interfacing.

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