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Improved Focalization of Electrical Microstimulation Using Microelectrode Arrays: A Modeling Study

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  • Sébastien Joucla
  • Blaise Yvert

Abstract

Extracellular electrical stimulation (EES) of the central nervous system (CNS) has been used empirically for decades, with both fundamental and clinical goals. Currently, microelectrode arrays (MEAs) offer new possibilities for CNS microstimulation. However, although focal CNS activation is of critical importance to achieve efficient stimulation strategies, the precise spatial extent of EES remains poorly understood. The aim of the present work is twofold. First, we validate a finite element model to compute accurately the electrical potential field generated throughout the extracellular medium by an EES delivered with MEAs. This model uses Robin boundary conditions that take into account the surface conductance of electrode/medium interfaces. Using this model, we determine how the potential field is influenced by the stimulation and ground electrode impedances, and by the electrical conductivity of the neural tissue. We confirm that current-controlled stimulations should be preferred to voltage-controlled stimulations in order to control the amplitude of the potential field. Second, we evaluate the focality of the potential field and threshold-distance curves for different electrode configurations. We propose a new configuration to improve the focality, using a ground surface surrounding all the electrodes of the array. We show that the lower the impedance of this surface, the more focal the stimulation. In conclusion, this study proposes new boundary conditions for the design of precise computational models of extracellular stimulation, and a new electrode configuration that can be easily incorporated into future MEA devices, either in vitro or in vivo, for a better spatial control of CNS microstimulation.

Suggested Citation

  • Sébastien Joucla & Blaise Yvert, 2009. "Improved Focalization of Electrical Microstimulation Using Microelectrode Arrays: A Modeling Study," PLOS ONE, Public Library of Science, vol. 4(3), pages 1-13, March.
  • Handle: RePEc:plo:pone00:0004828
    DOI: 10.1371/journal.pone.0004828
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