Literature DB >> 721972

Sources and terminations of callosal axons related to binaural and frequency maps in primary auditory cortex of the cat.

T J Imig, J F Brugge.   

Abstract

The distributions of sources and terminals of callosal fibers in the high-frequency representation of AI were related to binaural and frequency maps in combined anatomical and electrophysiological experiments. Sources of callosal axons were retrogradely labeled with HRP. Distributions of axon terminals were determined by autoradiographic labeling with [3H]-proline and anterograde degeneration following callosal section. Regions in which cells exhibit summation or ipsilateral dominance and suppression contain higher concentrations of sources and terminals of callosal fibers than do regions in which cells exhibit monaural contralateral responses or contralateral dominance and suppression. Callosal axon terminals aggregate into columns. In sections cut parallel to the cortical surface callosal columns take on complex forms that exhibit certain consistent features. Two prominent elongated columns separated by a narrow zone of sparse callosal innervation run in a rostrodorsal to caudoventral direction through AI crossing several octaves of the frequency representation. Ventral to these columns, along the AI-AII border, less densely labeled callosal columns are in evidence. Low frequency representations of AI are interconnected but details of their innervation patterns were not worked out. Outside of AI there are regions that contain complex configurations of callosal columns. Several morphologically distinct types of neurons, located in laminae III through VI, were retrogradely labeled following injections of HRP into the opposite AI. About 94% of callosal neurons are pyramidal cells of layers III and IV.

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Mesh:

Year:  1978        PMID: 721972     DOI: 10.1002/cne.901820406

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  36 in total

1.  Distributed representation of spectral and temporal information in rat primary auditory cortex.

Authors:  M P Kilgard; M M Merzenich
Journal:  Hear Res       Date:  1999-08       Impact factor: 3.208

2.  Modular organization of intrinsic connections associated with spectral tuning in cat auditory cortex.

Authors:  H L Read; J A Winer; C E Schreiner
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-03       Impact factor: 11.205

3.  Functional topography of cat primary auditory cortex: representation of tone intensity.

Authors:  C E Schreiner; J R Mendelson; M L Sutter
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

Review 4.  Thalamic and cortical pathways supporting auditory processing.

Authors:  Charles C Lee
Journal:  Brain Lang       Date:  2012-06-23       Impact factor: 2.381

5.  Functional organization of auditory cortical fields in the Mongolian gerbil (Meriones unguiculatus): binaural 2-deoxyglucose patterns.

Authors:  D Caird; H Scheich; R Klinke
Journal:  J Comp Physiol A       Date:  1991-01       Impact factor: 1.836

6.  Asymmetry in corticofugal modulation of frequency-tuning in mustached bat auditory system.

Authors:  Zhongju Xiao; Nobuo Suga
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-27       Impact factor: 11.205

Review 7.  The distributed auditory cortex.

Authors:  Jeffery A Winer; Charles C Lee
Journal:  Hear Res       Date:  2007-01-24       Impact factor: 3.208

8.  Bilateral cortical interaction: modulation of delay-tuned neurons in the contralateral auditory cortex.

Authors:  Jie Tang; Zhongju Xiao; Nobuo Suga
Journal:  J Neurosci       Date:  2007-08-01       Impact factor: 6.167

9.  Functional specificity of long-range intrinsic and interhemispheric connections in the visual cortex of strabismic cats.

Authors:  K E Schmidt; D S Kim; W Singer; T Bonhoeffer; S Löwel
Journal:  J Neurosci       Date:  1997-07-15       Impact factor: 6.167

10.  A comparison of visual callosal organization in normal, bilaterally enucleated and congenitally anophthalmic mice.

Authors:  R W Rhoades; R D Mooney; S E Fish
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

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