Literature DB >> 14534283

Spatial organization of frequency response areas and rate/level functions in the developing AI.

Ben H Bonham1, Steven W Cheung, Benoit Godey, Christoph E Schreiner.   

Abstract

The current study was conducted to extend our understanding of changes in spatial organization and response properties of cortical neurons in the developing mammalian forebrain. Extracellular multiunit responses to tones were recorded from a dense array of penetrations covering entire isofrequency contours in the primary auditory cortex (AI) of pentobarbital anesthetized kittens. Ages ranged from postnatal day 14 (P14), shortly after acquisition of normal auditory response thresholds, through postnatal day 111 (P111), when the kittens were largely mature. Spatial organization of the AI was tonotopically ordered by P14. The tonotopic gradient decreased with chronological maturation. At P14 the gradient was about 3.5 kHz/mm. By P111 it had declined to about 2.5 kHz/mm, so that the cortical region encompassing a fixed 3- to 15-kHz frequency range enlarged along its posterior-anterior dimension. Response properties of developing AI neurons changed in both frequency selectivity and intensity selectivity. The mean frequency tuning bandwidth increased with age. Initially, tuning bandwidths were narrow throughout the entire AI. With progressive maturation, broader bandwidths were observed in areas dorsal and ventral to a central region in which neurons remained narrowly tuned. The resulting spatial organization of tuning bandwidth was similar to that reported in adult cats. The majority of recording sites manifested nonmonotonic rate/level functions at all ages. However, the proportion of sites with monotonic rate/level functions increased with age. No spatial organization of rate/level functions (monotonic and nonmonotonic) was observed through P111. The relatively late development of bandwidth tuning in the AI compared with the early presence of tonotopic organization suggests that different developmental processes are responsible for structuring these two dimensions of acoustic selectivity.

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Year:  2003        PMID: 14534283     DOI: 10.1152/jn.00017.2003

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


  19 in total

1.  Specialization of primary auditory cortex processing by sound exposure in the "critical period".

Authors:  Haruka Nakahara; Li I Zhang; Michael M Merzenich
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-26       Impact factor: 11.205

2.  Development of spectral and temporal response selectivity in the auditory cortex.

Authors:  Edward F Chang; Shaowen Bao; Kazuo Imaizumi; Christoph E Schreiner; Michael M Merzenich
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-01       Impact factor: 11.205

3.  Effects of noise-induced hearing loss at young age on voice onset time and gap-in-noise representations in adult cat primary auditory cortex.

Authors:  Naotaka Aizawa; Jos J Eggermont
Journal:  J Assoc Res Otolaryngol       Date:  2006-01-12

Review 4.  [Early hearing experience and sensitive developmental periods].

Authors:  A Kral
Journal:  HNO       Date:  2009-01       Impact factor: 1.284

5.  Evaluation of techniques used to estimate cortical feature maps.

Authors:  Nalin Katta; Thomas L Chen; Paul V Watkins; Dennis L Barbour
Journal:  J Neurosci Methods       Date:  2011-08-25       Impact factor: 2.390

6.  Passive stimulation and behavioral training differentially transform temporal processing in the inferior colliculus and primary auditory cortex.

Authors:  Maike Vollmer; Ralph E Beitel; Christoph E Schreiner; Patricia A Leake
Journal:  J Neurophysiol       Date:  2016-10-12       Impact factor: 2.714

7.  Neonatal deafness results in degraded topographic specificity of auditory nerve projections to the cochlear nucleus in cats.

Authors:  Patricia A Leake; Gary T Hradek; Leila Chair; Russell L Snyder
Journal:  J Comp Neurol       Date:  2006-07-01       Impact factor: 3.215

8.  Selective Strengthening of Intracortical Excitatory Input Leads to Receptive Field Refinement during Auditory Cortical Development.

Authors:  Yujiao J Sun; Bao-Hua Liu; Huizhong W Tao; Li I Zhang
Journal:  J Neurosci       Date:  2018-12-26       Impact factor: 6.167

9.  Enriched acoustic environment after noise trauma reduces hearing loss and prevents cortical map reorganization.

Authors:  Arnaud J Noreña; Jos J Eggermont
Journal:  J Neurosci       Date:  2005-01-19       Impact factor: 6.167

10.  Increasing spectrotemporal sound density reveals an octave-based organization in cat primary auditory cortex.

Authors:  Arnaud J Noreña; Boris Gourévitch; Martin Pienkowski; Greg Shaw; Jos J Eggermont
Journal:  J Neurosci       Date:  2008-09-03       Impact factor: 6.167

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