Literature DB >> 12944528

Representation of species-specific vocalizations in the inferior colliculus of the guinea pig.

Daniel Suta1, Eugen Kvasnák, Jirí Popelár, Josef Syka.   

Abstract

The responses of individual neurons to 4 typical guinea pig vocalization calls (purr, chutter, chirp, and whistle) were recorded in the inferior colliculus (IC) of anesthetized guinea pigs. All calls elicited a response in about 80% of units. Unit selectivity for individual calls was low, given that a majority of neurons (55% of 124 units) responded to all vocalizations and only a small portion of neurons (3%) responded to only one call or did not respond to any of the calls (3%). In 15% of units, the response to one call was > or =25% stronger than the response to any other sound (tone, noise, and other calls); these neurons were selective for chirp or whistle, and no unit preferred chutter or purr. Neuronal activity provided information about the spectrotemporal patterns of the calls. Peristimulus time histograms (PSTHs) reflected the energy of the near-characteristic frequency band, and the population PSTH reliably matched the sound envelope for calls characterized by one or more short impulses (chirp, purr, and chutter) but did not exactly fit the envelope for whistle--a slow-modulated and relatively long call. Calculations based on firing rates indicated the approximate positions of the main spectral peaks but did not always reflect their relative magnitude. The time-reversed version of whistle elicited on average a weaker response than did the natural whistle (by 24%), but there were neurons with a significantly stronger response to the natural ("forward-selective," 30%) as well as to the time-reversed whistle ("reverse-selective," 15%). This study does not prove the existence of units selectively responding to animal calls, but it provides evidence for the encoding of the spectrotemporal acoustic patterns of vocalizations by IC units.

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Year:  2003        PMID: 12944528     DOI: 10.1152/jn.01175.2002

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


  44 in total

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Review 3.  Discriminating among complex signals: the roles of inhibition for creating response selectivities.

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4.  Formation and disruption of tonotopy in a large-scale model of the auditory cortex.

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5.  Representation of species-specific vocalizations in the medial geniculate body of the guinea pig.

Authors:  Daniel Suta; Jirí Popelár; Eugen Kvasnák; Josef Syka
Journal:  Exp Brain Res       Date:  2007-08-03       Impact factor: 1.972

6.  Experience is required for the maintenance and refinement of FM sweep selectivity in the developing auditory cortex.

Authors:  Khaleel A Razak; Marlin D Richardson; Zoltan M Fuzessery
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-11       Impact factor: 11.205

7.  Neural integration and enhancement from the inferior colliculus up to different layers of auditory cortex.

Authors:  Malgorzata M Straka; Dillon Schendel; Hubert H Lim
Journal:  J Neurophysiol       Date:  2013-05-29       Impact factor: 2.714

8.  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

9.  Responses of inferior collicular cells to species-specific vocalizations in normal and enucleated rats.

Authors:  T A Pincherli Castellanos; J Aitoubah; S Molotchnikoff; F Lepore; J-P Guillemot
Journal:  Exp Brain Res       Date:  2007-09-01       Impact factor: 1.972

10.  Electrophysiological validation of a human prototype auditory midbrain implant in a guinea pig model.

Authors:  Minoo Lenarz; Hubert H Lim; James F Patrick; David J Anderson; Thomas Lenarz
Journal:  J Assoc Res Otolaryngol       Date:  2006-10-31
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