Literature DB >> 7760117

Spontaneous and sound-evoked discharge characteristics of complex-spiking neurons in the dorsal cochlear nucleus of the unanesthetized decerebrate cat.

K Parham1, D O Kim.   

Abstract

1. We examined the spontaneous and sound-evoked discharge characteristics of 20 complex-spiking units recorded in the dorsal cochlear nucleus (DCN) of 15 unanesthetized, decerebrate cats. 2. The extracellularly recorded complex spikes consisted of bursts of two to five action potentials whose size gradually decreased during the burst. Complex spikes were observed both in the spontaneous and sound-evoked activity of the units in our sample. 3. The spontaneous rates (SRs) of DCN complex-spiking units ranged from 0 to 30 spikes/s. Spontaneous activity consisted of complex and simple (i.e., the common single neuronal action potential) spikes. Comparison of the SR distributions of the DCN complex-spiking units with that of a total sample of 194 DCN units (from 9 cats) suggests that the complex-spiking units tended to be in the lower half of the DCN SR distribution. 4. Sound-evoked discharges could consist of both complex and simple spikes. On the basis of their sound-driven responses, we divided the DCN complex-spiking units into two groups. The majority (15 of 20, 75%) were weakly driven by pure tones and inhibited by broadband noise. They tended to have broad response areas. Their response latencies to pure tone and noise stimuli were relatively long (10-20 ms). The recording depths of these units tended to be superficial (i.e., 10 of 15 units were located within 400 microns of the dorsal surface of the DCN). A minority (5 of 20, 25%) of the complex-spiking units were strongly driven by pure tone and broadband noise stimuli. These units had more clearly defined excitatory regions of response areas than the weakly driven units. Their response latencies to pure tone and noise stimuli were short (< 10 ms). The recording depths of these units tended to be deeper (i.e., 4 of 5 units were located at 400-700 microns) than those of the weakly driven units. 5. Intracellular recording and labeling studies of in vitro DCN slice preparations have correlated complex spikes with the superficially located cartwheel cells. Given the complex spikes of the units, many of which were located superficially, we suggest that our sample, particularly the weakly driven group of neurons, corresponds to the cartwheel cells. 6. Cartwheel cells are putative inhibitory interneurons whose axons primarily contact on the main projection neurons of DCN, the fusiform cells. The present finding of sound-evoked discharges by the superficially located complex-spiking units suggests that cartwheel cells should play a role in modifying the sound-evoked responses of the fusiform cells.

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Year:  1995        PMID: 7760117     DOI: 10.1152/jn.1995.73.2.550

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  16 in total

1.  Time course and permeation of synaptic AMPA receptors in cochlear nuclear neurons correlate with input.

Authors:  S M Gardner; L O Trussell; D Oertel
Journal:  J Neurosci       Date:  1999-10-15       Impact factor: 6.167

2.  Correlation of AMPA receptor subunit composition with synaptic input in the mammalian cochlear nuclei.

Authors:  S M Gardner; L O Trussell; D Oertel
Journal:  J Neurosci       Date:  2001-09-15       Impact factor: 6.167

3.  Dorsal cochlear nucleus response properties following acoustic trauma: response maps and spontaneous activity.

Authors:  Wei-Li Diana Ma; Eric D Young
Journal:  Hear Res       Date:  2006-04-19       Impact factor: 3.208

4.  Single-neuron recordings from unanesthetized mouse dorsal cochlear nucleus.

Authors:  Wei-Li Diana Ma; Stephan D Brenowitz
Journal:  J Neurophysiol       Date:  2011-11-09       Impact factor: 2.714

5.  Molecular layer inhibitory interneurons provide feedforward and lateral inhibition in the dorsal cochlear nucleus.

Authors:  Michael T Roberts; Laurence O Trussell
Journal:  J Neurophysiol       Date:  2010-08-18       Impact factor: 2.714

6.  Hazard functions and expected spike density functions for neuron spike activity in the cochlear nucleus of the cat.

Authors:  N Bibikov; T Imig; F Samson
Journal:  Neurosci Behav Physiol       Date:  2005-01

7.  Stimulus-dependent changes in optical responses of the dorsal cochlear nucleus using voltage-sensitive dye.

Authors:  F G Licari; M Shkoukani; J A Kaltenbach
Journal:  J Neurophysiol       Date:  2011-05-04       Impact factor: 2.714

8.  Granule cell activation of complex-spiking neurons in dorsal cochlear nucleus.

Authors:  K A Davis; E D Young
Journal:  J Neurosci       Date:  1997-09-01       Impact factor: 6.167

9.  Synaptic mechanisms for generating temporal diversity of auditory representation in the dorsal cochlear nucleus.

Authors:  Mu Zhou; Ya-Tang Li; Wei Yuan; Huizhong W Tao; Li I Zhang
Journal:  J Neurophysiol       Date:  2014-12-04       Impact factor: 2.714

Review 10.  Neural mechanisms underlying somatic tinnitus.

Authors:  Susan Shore; Jianxun Zhou; Seth Koehler
Journal:  Prog Brain Res       Date:  2007       Impact factor: 2.453

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