Literature DB >> 7400400

Patterns of cortico-cortical connections related to tonotopic maps in cat auditory cortex.

T J Imig, R A Reale.   

Abstract

Topographic distributions of cortico-cortical projections from the primary (AI), anterior (A), posterior (P), ventroposterior (VP), and second (AII) auditory fields were studied in relation to tonotopic maps in combined anatomical and electrophysiological experiments. Distributions of axon terminals were determined by autoradiographic labeling with tritiated proline and leucine. Each of fields A, AI, P, and VP is connected with the other three in the same hemisphere as well as with a number of other auditory cortical areas. Additionally, neurons in each of the fields studied were found to project to the lateral bank of the collateral fissure. In general, regions near the injection site receive more densely labeled projections than do more distant targets. Neurons in each field were found to project to one or more areas in th opposite hemisphere. Only similar portions of the best-frequency representations in fields A, AI, P, and VP are interconnected. A single isotope injection generally produced multiple patches of labeling within each of several cortical fields. Within AI, projections from contralateral fields A and AI and from ipsilateral fields A and P terminate in patches which are often elongated in a direction parallel to the low-to-high best-frequency gradient. A divergence in the projections from one field upon another is apparent in many experiments. Within fields A, AI, P, and VP, patches of label are distributed along a band of cortex oriented parallel to isofrequency lines.

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Mesh:

Year:  1980        PMID: 7400400     DOI: 10.1002/cne.901920208

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


  35 in total

1.  Areas of cat auditory cortex as defined by neurofilament proteins expressing SMI-32.

Authors:  Jeffrey G Mellott; Estel Van der Gucht; Charles C Lee; Andres Carrasco; Jeffery A Winer; Stephen G Lomber
Journal:  Hear Res       Date:  2010-04-27       Impact factor: 3.208

2.  Sex-dependent hemispheric asymmetries for processing frequency-modulated sounds in the primary auditory cortex of the mustached bat.

Authors:  Stuart D Washington; Jagmeet S Kanwal
Journal:  J Neurophysiol       Date:  2012-05-30       Impact factor: 2.714

3.  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

4.  Interconnections of the auditory cortical fields of the cat with the cingulate and parahippocampal cortices.

Authors:  E M Rouiller; G M Innocenti; F De Ribaupierre
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

5.  Connections of cat auditory cortex: I. Thalamocortical system.

Authors:  Charles C Lee; Jeffery A Winer
Journal:  J Comp Neurol       Date:  2008-04-20       Impact factor: 3.215

6.  Connections of cat auditory cortex: III. Corticocortical system.

Authors:  Charles C Lee; Jeffery A Winer
Journal:  J Comp Neurol       Date:  2008-04-20       Impact factor: 3.215

7.  Connections of cat auditory cortex: II. Commissural system.

Authors:  Charles C Lee; Jeffery A Winer
Journal:  J Comp Neurol       Date:  2008-04-20       Impact factor: 3.215

8.  Intrinsic inter- and intralaminar connections and their relationship to the tonotopic map in cat primary auditory cortex.

Authors:  M N Wallace; L M Kitzes; E G Jones
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

9.  Topographical organization of the cortical afferent connections to the cortex of the anterior ectosylvian sulcus in the cat.

Authors:  F Reinoso-Suárez; J M Roda
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

10.  Auditory corticocortical interconnections in the cat: evidence for parallel and hierarchical arrangement of the auditory cortical areas.

Authors:  E M Rouiller; G M Simm; A E Villa; Y de Ribaupierre; F de Ribaupierre
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

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