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Effects of contralateral sound stimulation on unit activity of ventral cochlear nucleus neurons

dc.contributor.authorLu, J.en_US
dc.contributor.authorBledsoe, Sanford C., Jr.en_US
dc.contributor.authorSumner, C. J.en_US
dc.contributor.authorShore, Susan E.en_US
dc.date.accessioned2006-09-11T17:53:54Z
dc.date.available2006-09-11T17:53:54Z
dc.date.issued2003-12en_US
dc.identifier.citationShore, S. E.; Sumner, C. J.; Bledsoe, S. C.; Lu, J.; (2003). "Effects of contralateral sound stimulation on unit activity of ventral cochlear nucleus neurons." Experimental Brain Research 153(4): 427-435. <http://hdl.handle.net/2027.42/46533>en_US
dc.identifier.issn1432-1106en_US
dc.identifier.issn0014-4819en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46533
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12961054&dopt=citationen_US
dc.description.abstractThe cochlear nucleus (CN) commissural connection represents the first opportunity for convergence of binaural information in the auditory brainstem. All major neuron types in the ventral CN (VCN) are innervated by a diverse population of cells in the contralateral VCN. This study examined the effect of contralateral sound stimulation on the spontaneous rates (SRs) of neurons in the VCN. Unit activity was recorded with silicon-substrate multichannel probes which allowed recordings from up to 16 sites simultaneously. On average, 30% of units showed short-latency (often only 2 ms greater than the latencies of ipsilateral sound-evoked responses) inhibition of SR by wideband contralateral noise bursts. Fewer units (4.5%) were excited by contralateral noise at sound levels low enough to exclude excitation by acoustic crossover. Both regular and irregular units in the anterior VCN (AVCN) and posterior VCN (PVCN) were inhibited by contralateral sound. Decrements in SR followed a monotonic function with increases in contralateral sound level, except where responses could be attributed to acoustic crossover. Restricting the contralateral noise bandwidth resulted in a frequency-specific inhibition, dominated by frequencies at and below the ipsilateral BF of the unit, consistent with anatomical findings of the tonotopic organization of the CN commissural pathway. The latencies of these effects are compatible with mono, di and tri-synaptic connections reflecting CN commissural pathway effects.en_US
dc.format.extent393536 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherAuditoryen_US
dc.subject.otherCommissural Pathwayen_US
dc.subject.otherSingle Unit Physiologyen_US
dc.subject.otherLifeSciencesen_US
dc.subject.otherAuditory Brainstemen_US
dc.subject.otherNeural Pathwaysen_US
dc.titleEffects of contralateral sound stimulation on unit activity of ventral cochlear nucleus neuronsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology, University of Michigan, USAen_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology, University of Michigan, USA; 1301 E. Ann St., Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology, University of Michigan, USAen_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology, University of Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12961054en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46533/1/221_2003_Article_1610.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00221-003-1610-6en_US
dc.identifier.sourceExperimental Brain Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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