Literature DB >> 3367194

Neural correlations in the dorsal cochlear nucleus: pairs of units with similar response properties.

H F Voigt1, E D Young.   

Abstract

1. Cross-correlation analysis of simultaneously recorded spike trains can be used to gain insight into functional interactions among neurons. In this paper, we report on cross-correlation analysis of neuron pairs in the dorsal cochlear nucleus (DCN) of the cat. Neuron pairs were isolated with two independent electrodes, which allow systematic study of the effects on correlation of distances between units and differences in their best frequencies (BFs). The data in this paper were obtained from 51 pairs consisting of two neurons of the same type. 2. Cross-correlograms were obtained for 35 pairs composed of type IV units, which are recorded from the principal cells of the DCN. Pairs of type IV units with correlated activities give cross-correlograms with increased correlation near zero delay. This feature is called a central mound (CM) and most likely results from shared excitatory or shared inhibitory inputs. 3. Records of spontaneous activity were obtained from 31 pairs of type IV units. Six of these pairs have correlated spontaneous activities. All six pairs have BFs that differ by less than 0.2 octaves. The shared input inducing these correlations must be a spontaneously active and tonotopically organized projection, like the auditory nerve. Type II units, thought to be DCN inhibitory interneurons that project to type IV units, are not spontaneously active, and thus cannot be the cause of correlated spontaneous activity. Similarly, cochlear granule cells, whose axons project orthogonally to the tonotopic sheets of DCN, cannot be the cause of correlated spontaneous activity because their projection is not confined tonotopically. 4. Stimulus-driven activities were studied for 12 type IV pairs that have uncorrelated spontaneous activities. Five of these pairs have correlated driven activities, with CMs whose sizes depend on the frequency and sound level of the acoustic stimulus. A frequency vs. sound level correlation response map shows the V-shaped tuning properties of the correlation-inducing mechanism. The properties of stimulus-driven correlation in these type IV pairs are consistent with the hypothesis that the correlation is induced by shared input from DCN type II units, although this is not the only possibility. 5. All six type IV pairs with correlated spontaneous activities have correlated driven activities. In five of these pairs, the degree of correlation decreases from its value with spontaneous activity when a low-level acoustic stimulus is applied. Three of these five pairs were tested at higher stimulus levels.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1988        PMID: 3367194     DOI: 10.1152/jn.1988.59.3.1014

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


  10 in total

1.  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

2.  Action potential timing precision in dorsal cochlear nucleus pyramidal cells.

Authors:  Sarah E Street; Paul B Manis
Journal:  J Neurophysiol       Date:  2007-04-18       Impact factor: 2.714

3.  Independent population coding of speech with sub-millisecond precision.

Authors:  Jose A Garcia-Lazaro; Lucile A C Belliveau; Nicholas A Lesica
Journal:  J Neurosci       Date:  2013-12-04       Impact factor: 6.167

4.  Response classes in the dorsal cochlear nucleus and its output tract in the chloralose-anesthetized cat.

Authors:  P X Joris
Journal:  J Neurosci       Date:  1998-05-15       Impact factor: 6.167

5.  Computer simulation of shared input among projection neurons in the dorsal cochlear nucleus.

Authors:  K A Davis; H F Voigt
Journal:  Biol Cybern       Date:  1996-05       Impact factor: 2.086

6.  Muscarinic acetylcholine receptors control baseline activity and Hebbian stimulus timing-dependent plasticity in fusiform cells of the dorsal cochlear nucleus.

Authors:  Roxana A Stefanescu; Susan E Shore
Journal:  J Neurophysiol       Date:  2016-12-21       Impact factor: 2.714

7.  Subthreshold oscillations generated by TTX-sensitive sodium currents in dorsal cochlear nucleus pyramidal cells.

Authors:  Paul B Manis; Scott C Molitor; Huijie Wu
Journal:  Exp Brain Res       Date:  2003-09-24       Impact factor: 1.972

8.  Neural modeling of the dorsal cochlear nucleus: cross-correlation analysis of short-duration tone-burst responses.

Authors:  K A Davis; H F Voigt
Journal:  Biol Cybern       Date:  1994       Impact factor: 2.086

9.  NMDA Receptors Mediate Stimulus-Timing-Dependent Plasticity and Neural Synchrony in the Dorsal Cochlear Nucleus.

Authors:  Roxana A Stefanescu; Susan E Shore
Journal:  Front Neural Circuits       Date:  2015-11-20       Impact factor: 3.492

10.  Inhibitory interneurons in a brainstem circuit adjust their inhibitory motifs to process multimodal input.

Authors:  Calvin Wu; Susan E Shore
Journal:  J Physiol       Date:  2020-11-09       Impact factor: 5.182

  10 in total

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