Title of article :
A novel electrode array for diameter-dependent control of axonal excitability: a Simulation study
Author/Authors :
Z.، Lertmanorat, نويسنده , , D.M.، Durand, نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
-1241
From page :
1242
To page :
0
Abstract :
Electrical extracellular stimulation of peripheral nerve activates the large-diameter motor fibers before the small ones, a recruitment order opposite the physiological recruitment of myelinated motor fibers during voluntary muscle contraction. Current methods to solve this problem require a long-duration stimulus pulse which could lead to electrode corrosion and nerve damage. The hypothesis that the excitability of specific diameter fibers can be suppressed by reshaping the profile of extracellular potential along the axon using multiple electrodes is tested using computer simulations in two different volume conductors. Simulations in a homogenous medium with a nine-contact electrode array show that the current excitation threshold (I/sub th/) of large diameter axons (13-17 (mu)m) (0.6-3.0 mA) is higher than that of small-diameter axons (2-7 (mu)m) (0.4-0.7 mA) with 200-(mu)m axon-electrode distance and 10-(mu)s stimulus pulse. The electrode array is also tested in a three-dimensional finite-element model of the sacral root model of dog (ventral root of S3). A single cathode activates large-diameter axons before activating small axons. However, a nine-electrode array activates 50% of small axons while recruiting only 10% of large ones and activates 90% of small axons while recruiting only 50% of large ones. The simulations suggest that the near-physiological recruitment order can be achieved with an electrode array. The diameter selectivity of the electrode array can be controlled by the electrode separation and the method is independent of pulse width.
Journal title :
IEEE Transactions on Biomedical Engineering
Serial Year :
2004
Journal title :
IEEE Transactions on Biomedical Engineering
Record number :
80495
Link To Document :
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