Literature DB >> 23545427

The dominant role of inhibition in creating response selectivities for communication calls in the brainstem auditory system.

George D Pollak1.   

Abstract

This review is concerned with how communication calls are processed and represented by populations of neurons in both the inferior colliculus (IC), the auditory midbrain nucleus, and the dorsal nucleus of the lateral lemniscus (DNLL), the nucleus just caudal to the IC. The review has five sections where focus in each section is on inhibition and its role in shaping response selectivity for communication calls. In the first section, the lack of response selectivity for calls in DNLL neurons is presented and discusses why inhibition plays virtually no role in shaping selectivity. In the second section, the lack of selectivity in the DNLL is contrasted with the high degree of response selectivity in the IC. The third section then reviews how inhibition in the IC shapes response selectivities for calls, and how those selectivities can create a population response with a distinctive response profile to a particular call, which differs from the population profile evoked by any other call. The fourth section is concerned with the specifics of inhibition in the IC, and how the interaction of excitation and inhibition creates directional selectivities for frequency modulations, one of the principal acoustic features of communication signals. The two major hypotheses for directional selectivity are presented. One is the timing hypothesis, which holds that the precise timing of excitation relative to inhibition is the feature that shapes directionality. The other hypothesis is that the relative magnitudes of excitation and inhibition are the dominant features that shape directionality, where timing is relatively unimportant. The final section then turns to the role of serotonin, a neuromodulator that can markedly change responses to calls in the IC. Serotonin provides a linkage between behavioral states and processing. This linkage is discussed in the final section together with the hypothesis that serotonin acts to enhances the contrast in the population responses to various calls over and above the distinctive population responses that were created by inhibition. This article is part of a Special Issue entitled "Communication Sounds and the Brain: New Directions and Perspectives".
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  DNLL; EPSP; FM; IC; IPSP; MΩ; PSP; SI; STRF; Similarity index; dorsal nucleus of the lateral lemniscus; excitatory post-synaptic potential; frequency modulation; inferior colliculus; inhibitory post-synaptic potential; mV; megaohm; millivolt; post-synaptic potential; spectrotemporal receptive field

Mesh:

Substances:

Year:  2013        PMID: 23545427      PMCID: PMC3778109          DOI: 10.1016/j.heares.2013.03.001

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  59 in total

1.  Combination sensitivity and processing of communication calls in the inferior colliculus of the Moustached Bat Pteronotus parnellii.

Authors:  Christine V Portfors
Journal:  An Acad Bras Cienc       Date:  2004-06-08       Impact factor: 1.753

Review 2.  Context-dependent modulation of auditory processing by serotonin.

Authors:  L M Hurley; I C Hall
Journal:  Hear Res       Date:  2010-12-25       Impact factor: 3.208

3.  Tuning for spectro-temporal modulations as a mechanism for auditory discrimination of natural sounds.

Authors:  Sarah M N Woolley; Thane E Fremouw; Anne Hsu; Frédéric E Theunissen
Journal:  Nat Neurosci       Date:  2005-09-04       Impact factor: 24.884

4.  Neural mechanisms underlying selectivity for the rate and direction of frequency-modulated sweeps in the inferior colliculus of the pallid bat.

Authors:  Zoltan M Fuzessery; Marlin D Richardson; Michael S Coburn
Journal:  J Neurophysiol       Date:  2006-06-21       Impact factor: 2.714

5.  Response properties and location of neurons selective for sinusoidal frequency modulations in the inferior colliculus of the big brown bat.

Authors:  Qi Yue; John H Casseday; Ellen Covey
Journal:  J Neurophysiol       Date:  2007-07-18       Impact factor: 2.714

6.  Syllable acoustics, temporal patterns, and call composition vary with behavioral context in Mexican free-tailed bats.

Authors:  Kirsten M Bohn; Barbara Schmidt-French; Sean T Ma; George D Pollak
Journal:  J Acoust Soc Am       Date:  2008-09       Impact factor: 1.840

7.  Efficient encoding of vocalizations in the auditory midbrain.

Authors:  Lars A Holmstrom; Lonneke B M Eeuwes; Patrick D Roberts; Christine V Portfors
Journal:  J Neurosci       Date:  2010-01-20       Impact factor: 6.167

8.  GABA shapes selectivity for the rate and direction of frequency-modulated sweeps in the auditory cortex.

Authors:  Khaleel A Razak; Zoltan M Fuzessery
Journal:  J Neurophysiol       Date:  2009-06-24       Impact factor: 2.714

9.  Coding and processing in the auditory systems of FM-signal-producing bats.

Authors:  N Suga; P Schlegel
Journal:  J Acoust Soc Am       Date:  1973-07       Impact factor: 1.840

10.  Serotonin differentially modulates responses to tones and frequency-modulated sweeps in the inferior colliculus.

Authors:  L M Hurley; G D Pollak
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

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  12 in total

1.  Context-dependent fluctuation of serotonin in the auditory midbrain: the influence of sex, reproductive state and experience.

Authors:  Jessica L Hanson; Laura M Hurley
Journal:  J Exp Biol       Date:  2013-11-06       Impact factor: 3.312

2.  GABAA receptors contribute more to rate than temporal coding in the IC of awake mice.

Authors:  Boris Gourévitch; Elena J Mahrt; Warren Bakay; Cameron Elde; Christine V Portfors
Journal:  J Neurophysiol       Date:  2019-11-13       Impact factor: 2.714

Review 3.  Subcortical pathways: Towards a better understanding of auditory disorders.

Authors:  Richard A Felix; Boris Gourévitch; Christine V Portfors
Journal:  Hear Res       Date:  2018-01-31       Impact factor: 3.208

4.  Serotonin, estrus, and social context influence c-Fos immunoreactivity in the inferior colliculus.

Authors:  Jessica L Hanson; Laura M Hurley
Journal:  Behav Neurosci       Date:  2016-09-22       Impact factor: 1.912

5.  The superior paraolivary nucleus shapes temporal response properties of neurons in the inferior colliculus.

Authors:  Richard A Felix; Anna K Magnusson; Albert S Berrebi
Journal:  Brain Struct Funct       Date:  2014-06-29       Impact factor: 3.270

6.  Extracellular Molecular Markers and Soma Size of Inhibitory Neurons: Evidence for Four Subtypes of GABAergic Cells in the Inferior Colliculus.

Authors:  Nichole L Beebe; Jesse W Young; Jeffrey G Mellott; Brett R Schofield
Journal:  J Neurosci       Date:  2016-04-06       Impact factor: 6.167

7.  High-field functional magnetic resonance imaging of vocalization processing in marmosets.

Authors:  Srivatsun Sadagopan; Nesibe Z Temiz-Karayol; Henning U Voss
Journal:  Sci Rep       Date:  2015-06-19       Impact factor: 4.379

Review 8.  Central gain control in tinnitus and hyperacusis.

Authors:  Benjamin D Auerbach; Paulo V Rodrigues; Richard J Salvi
Journal:  Front Neurol       Date:  2014-10-24       Impact factor: 4.003

9.  Optimal features for auditory categorization.

Authors:  Shi Tong Liu; Pilar Montes-Lourido; Xiaoqin Wang; Srivatsun Sadagopan
Journal:  Nat Commun       Date:  2019-03-21       Impact factor: 14.919

10.  Responses to Social Vocalizations in the Dorsal Cochlear Nucleus of Mice.

Authors:  Patrick D Roberts; Christine V Portfors
Journal:  Front Syst Neurosci       Date:  2015-12-16
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