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1.
IEEE Trans Neural Syst Rehabil Eng ; 25(8): 1353-1362, 2017 08.
Article in English | MEDLINE | ID: mdl-27831887

ABSTRACT

This study models induced electric fields, and their gradient, produced by pulsatile current stimulation of submillimeter inductors for cochlear implantation. Using finite-element analysis, the lower chamber of the cochlea, scala tympani, is modeled as a cylindrical structure filled with perilymph bounded by tissue, bone, and cochlear neural elements. Single inductors as well as an array of inductors are modeled. The coil strength (~100 nH) and excitation parameters (peak current of 1-5 A, voltages of 16-20 V) are based on a formative feasibility study conducted by our group. In that study, intracochlear micromagnetic stimulation achieved auditory activation as measured through the auditory brainstem response in a feline model. With respect to the finite element simulations, axial symmetry of the inductor geometry is exploited to improve computation time. It is verified that the inductor coil orientation greatly affects the strength of the induced electric field and thereby the ability to affect the transmembrane potential of nearby neural elements. Furthermore, upon comparing an array of micro-inductors with a typical multi-site electrode array, magnetically excited arrays retain greater focus in terms of the gradient of induced electric fields. Once combined with further in vivo analysis, this modeling study may enable further exploration of the mechanism of magnetically induced, and focused neural stimulation.


Subject(s)
Cochlea/physiology , Cochlea/radiation effects , Electric Stimulation Therapy/methods , Evoked Potentials, Auditory, Brain Stem/physiology , Evoked Potentials, Auditory, Brain Stem/radiation effects , Models, Biological , Computer Simulation , Dose-Response Relationship, Radiation , Finite Element Analysis , Humans , Magnetic Field Therapy/methods , Magnetic Fields , Radiation Dosage
2.
J Neurosci Methods ; 93(1): 27-35, 1999 Oct 30.
Article in English | MEDLINE | ID: mdl-10598862

ABSTRACT

A new class of brain implant technology was developed that allows the simultaneous recording of voltage signals from many individual neurons in the cerebral cortex during cognitive tasks. The device allows recording from 49 independent positions spanning a 2 x 2-mm region of neural tissue. The recording electrodes are positioned in a square grid with 350 microm spacing, and each microelectrode can be precisely independently vertically positioned using a hydraulic microdrive. The device utilizes ultrafine, sharp iridium microelectrodes that minimize mechanical disturbance of the region near the electrode tip and produce low noise neuronal recordings. The total weight of this device is less than 20 g, and the device is reusable. The implant device has been used for transdural recordings in primary somatosensory and auditory cortices of marmosets, owl monkeys, and rats. On a typical day, one-third of the microelectrodes yield well-discriminated single neuron action potential waveforms. Additional array electrodes yield lower amplitude driven multiunit activity. The average signal-to-noise ratio of discriminated action potential waveforms 6 months after implantation was greater than 9. Simple design alternatives are discussed that can increase the number of electrodes in the array and the depths at which dense array recordings can be achieved.


Subject(s)
Biocompatible Materials , Cerebral Cortex/physiology , Electrodes, Implanted , Neurons/physiology , Animals , Aotus trivirgatus , Behavior, Animal/physiology , Callithrix , Equipment Design , Rats
3.
Science ; 280(5368): 1439-43, 1998 May 29.
Article in English | MEDLINE | ID: mdl-9603734

ABSTRACT

The brain's cerebral cortex decomposes visual images into information about oriented edges, direction and velocity information, and color. How does the cortex decompose perceived sounds? A reverse correlation technique demonstrates that neurons in the primary auditory cortex of the awake primate have complex patterns of sound-feature selectivity that indicate sensitivity to stimulus edges in frequency or in time, stimulus transitions in frequency or intensity, and feature conjunctions. This allows the creation of classes of stimuli matched to the processing characteristics of auditory cortical neurons. Stimuli designed for a particular neuron's preferred feature pattern can drive that neuron with higher sustained firing rates than have typically been recorded with simple stimuli. These data suggest that the cortex decomposes an auditory scene into component parts using a feature-processing system reminiscent of that used for the cortical decomposition of visual images.


Subject(s)
Auditory Cortex/physiology , Neurons/physiology , Sound , Acoustic Stimulation , Action Potentials , Animals , Aotidae , Brain Mapping , Evoked Potentials, Auditory , Microelectrodes
4.
J Neurosci ; 18(4): 1559-70, 1998 Feb 15.
Article in English | MEDLINE | ID: mdl-9454861

ABSTRACT

This paper concerns the characterization of performance and perceptual learning of somatosensory interval discrimination. The purposes of this study were to define (1) the performance characteristics for interval discrimination in the somatosensory system by naive adult humans, (2) the normal capacities for improvement in somatosensory interval discrimination, and (3) the extent of generalization of interval discrimination learning. In a two-alternative forced choice procedure, subjects were presented with two pairs of vibratory pulses. One pair was separated in time by a fixed base interval; a second pair was separated by a target interval that was always longer than the base interval. Subjects indicated which pair was separated by the target interval. The length of the target interval was varied adaptively to determine discrimination thresholds. After initial determination of naive abilities, subjects were trained for 900 trials per day at base intervals of either 75 or 125 msec for 10-15 d. Significant improvements in thresholds resulted from training. Learning at the trained base interval generalized completely across untrained skin locations on the trained hand and to the corresponding untrained skin location in the contralateral hand. The learning partially generalized to untrained base intervals similar to the trained one, but not to more distant base intervals. Learning with somatosensory stimuli generalized to auditory stimuli presented at comparable base intervals. These results demonstrate temporal specificity in somatosensory interval discrimination learning that generalizes across skin location, hemisphere, and modality.


Subject(s)
Brain/physiology , Discrimination Learning/physiology , Discrimination, Psychological/physiology , Sensation/physiology , Skin Physiological Phenomena , Adult , Humans , Male , Middle Aged , Time Factors
5.
J Neurophysiol ; 78(5): 2503-17, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9356401

ABSTRACT

Monkey cutaneous SAI and RA responses to raised and depressed scanned patterns: effects of width, height, orientation, and a raised surround. J. Neurophysiol. 78: 2503-2517, 1997. The aim of this study was to examine the slowly adapting type I (SAI) and rapidly adapting (RA) primary afferent representation of raised and depressed surface features. Isolated, raised, and depressed squares and small raised squares with a circular surround were scanned across the receptive fields of SAI and RA mechanoreceptive afferents innervating the distal fingerpads of the rhesus monkey. Pattern height ranged from -620 to +620 micron and width ranged from 0.2 to 7.0 mm. The surround radii ranged from 3.0 to 7.0 mm. Previous combined psychophysical and neurophysiological studies have provided evidence that SAI afferent responses are responsible for the perception of spatial form and texture and that RA afferents are responsible for the detection of stimuli that produce minute skin motion (flutter, slip, microgeometric surface features). Our results strengthen these hypotheses. Response properties shared by both SAI and RA afferent types were that both responded only to the edges of the larger raised and depressed patterns, both responded to falling edges half as vigorously as to rising edges, both responded to rising and falling edges with impulse rates that were proportional to the sine of the angle between the edge and the scanning direction, and both had suppressed responses to a small raised surface feature when a raised surround was closer than 6 mm. Response differences consistent with the hypothesis that SAI afferents are specialized for the representation of form were that SAI responses were confined to areas around the features that evoked them in areas that were 40-50% smaller than the comparable RA response areas, SAI responses were more than four times more sensitive to stimulus height than were RA afferents over the range from 280 to 620 micron, and SAI (but not RA) afferents responded 20-50% more vigorously to corners than to edges. Response differences consistent with the hypothesis that RA afferents are specialized for the detection of minute surfaces features were that only RA afferents responded to very small surface depressions, depressed squares 0.8 mm wide, that were detectable by palpation. Mechanisms underlying the many differences in SAI and RA response properties are discussed.


Subject(s)
Afferent Pathways/physiology , Mechanoreceptors/physiology , Median Nerve/physiology , Neurons/physiology , Skin/innervation , Ulnar Nerve/physiology , Action Potentials/physiology , Animals , Fingers/innervation , Macaca mulatta , Movement , Nerve Fibers/physiology , Orientation , Physical Stimulation , Reaction Time , Regression Analysis , Torque , Vibration
6.
J Neurosci ; 17(19): 7480-9, 1997 Oct 01.
Article in English | MEDLINE | ID: mdl-9295394

ABSTRACT

Tactile pattern recognition depends on form and texture perception. A principal dimension of texture perception is roughness, the neural coding of which was the focus of this study. Previous studies have shown that perceived roughness is not based on neural activity in the Pacinian or cutaneous slowly adapting type II (SAII) neural responses or on mean impulse rate or temporal patterning in the cutaneous slowly adapting type I (SAI) or rapidly adapting (RA) discharge evoked by a textured surface. However, those studies found very high correlations between roughness scaling by humans and measures of spatial variation in SAI and RA firing rates. The present study used textured surfaces composed of dots of varying height (280-620 micron) and diameter (0.25-2.5 mm) in psychophysical and neurophysiological experiments. RA responses were affected least by the range of dot diameters and heights that produced the widest variation in perceived roughness, and these responses could not account for the psychophysical data. In contrast, spatial variation in SAI impulse rate was correlated closely with perceived roughness over the whole stimulus range, and a single measure of SAI spatial variation accounts for the psychophysical data in this (0.974 correlation) and two previous studies. Analyses based on the possibility that perceived roughness depends on both afferent types suggest that if the RA response plays a role in roughness perception, it is one of mild inhibition. These data reinforce the hypothesis that SAI afferents are mainly responsible for information about form and texture whereas RA afferents are mainly responsible for information about flutter, slip, and motion across the skin surface.


Subject(s)
Adaptation, Physiological , Mechanoreceptors/physiology , Memory/physiology , Touch/physiology , Adult , Female , Humans , Male , Nervous System Physiological Phenomena , Physical Stimulation , Psychophysics/methods , Time Factors
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