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dc.contributor.advisorBertrand Delgutte and Donald K. Eddington.en_US
dc.contributor.authorLitvak, Leonid, 1973-en_US
dc.contributor.otherHarvard University--MIT Division of Health Sciences and Technology.en_US
dc.date.accessioned2005-05-19T14:43:02Z
dc.date.available2005-05-19T14:43:02Z
dc.date.copyright2002en_US
dc.date.issued2002en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/16817
dc.descriptionThesis (Ph.D.)--Harvard--Massachusetts Institute of Technology Division of Health Sciences and Technology, 2002.en_US
dc.descriptionIncludes bibliographical references (p. 169-184).en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.description.abstractCochlear implants are prosthetic devices that seek to restore hearing in profoundly deaf patients by electrically stimulating the auditory-nerve (AN). With current implants, the representation of the sound waveform in temporal discharge patterns of the auditory nerve is severely distorted. The distortion is particularly significant at higher (>600 Hz) frequencies, for which the period of the electric stimulus is near the AN refractory period. For example, in response to a 1000-Hz pulse train, most AN fibers may fire on every other stimulus cycle, so that the AN population would represent half of the stimulus frequency rather than the actual frequency. Rubinstein et al. [Hearing. Res. 127, 108] proposed that the coding of electric waveforms in cochlear implants can be improved if a sustained, electric high-rate (5 kpps) desynchronizing pulse train (DPT) is presented in addition to the information-carrying electric stimulus. The DPT may amplify the inherent noise in ANfibers so as to produce ongoing, stochastic discharges similar to the spontaneous activity in a healthy hear. We tested this hypothesis by recording responses of ANfibers of deafened cats to sustained electric pulse trains. For most fibers, responses to the DPT showed adaptation during the first 2 minutes, followed by a sustained response for the remainder of the 10-minute stimulus. These sustained responses partially resembled spontaneous activity in terms of discharge rate and interspike interval distributions. AN fibers were extremely sensitive to modulations of the DPT, responding tomodulations as small as 0.5%.en_US
dc.description.abstract(cont.) Responses to sinusoidal modulations resembled AN responses to pure tones over a 15-25 dB range of modulation depths. Responses to complex modulations simultaneously represented several spectral components of the modulator in their temporal discharge patterns. However, for modulation depths above 10%, the representation of both sinusoidal and complex modulators was more distorted. These results demonstrate that strategies that incorporate a DPT, and that use low modulation depths to encode sounds, may evoke AN responses that more accurately represent the modulator in their temporal discharge patterns. If the central nervous system can utilize this information, then these strategies may substantially improve performance enjoyed by cochlear implant users.en_US
dc.description.statementofresponsibilityby Leonid Litvak.en_US
dc.format.extent184 p.en_US
dc.format.extent1958964 bytes
dc.format.extent1958723 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/pdf
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectHarvard University--MIT Division of Health Sciences and Technology.en_US
dc.titleTowards a better speech processor for cochlear implants : auditory- nerve responses to high-rate electric pulse trainsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
dc.identifier.oclc50658001en_US


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