Literature DB >> 7925809

Neuronal responsiveness in areas 19 and 21a, and the posteromedial lateral suprasylvian cortex of the cat.

K Toyama1, K Mizobe, E Akase, T Kaihara.   

Abstract

Responsiveness to slits and pattern stimuli was quantified in a total of 68 cells sampled in the posterior extreme of the lateral suprasylvian (PS) cortex as response indices. The cells were studied in relationship to their locations in several subareas of the PS cortex, including areas 19 (n = 15) and 21a (n = 32) and the posteromedial lateral suprasylvian cortex (PMLS; n = 21). These subareas were identified based on retrograde labelling from area 17 and also supplemented with photic responsiveness. This analysis revealed that each cortical area contains cells expressing different combinations of stimulus features. Area 19 contained two major groups of cells: (1) those with strong end-stop selectivity combined with moderate orientation or direction selectivity, and (2) those with weak end-stop selectivity combined with strong orientation selectivity. The groups of cells with strong or moderate orientation selectivity showed a strong preference for stripe over visual noise patterns and relatively large modulatory responses to motion of individual stripes. The PMLS contained one major group of cells with strong end-stop and direction selectivities and with poor orientation selectivity. They also showed stronger preference for visual noise than cells in the other cortical areas and rather weak modulatory responses. Area 21a contained only one group of cells with strong orientation selectivity and length summation property rather than end-stop selectivity, and they also lacked direction selectivity. These cells exhibited a strong preference for stripe patterns and moderate or weak modulatory responses. Altogether, these findings indicate that each cortical area is specialized in expressing different stimulus features. The two groups of cells in area 19 may encode the position and motion of discontinuous visual elements such as corners and line ends and continuous elements such as lines and edges. PMLS cells may encode the motion of single elements or associated motion of multiple discontinuous elements such as textures and backgrounds. Area 21a cells may specifically encode the orientation of long, continuous elements such as lines and edges. In support of this view, two types of statistical analyses demonstrated that the combinations of the response properties expressed in individual PS cells are highly correlated with their locations in cortical areas and that the anatomical locations of individual PS cells are reliably predicted from the sets of response indices expressed in these cells.

Mesh:

Year:  1994        PMID: 7925809     DOI: 10.1007/bf00239595

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  31 in total

1.  The analysis of visual motion: a comparison of neuronal and psychophysical performance.

Authors:  K H Britten; M N Shadlen; W T Newsome; J A Movshon
Journal:  J Neurosci       Date:  1992-12       Impact factor: 6.167

2.  Functional differentiation between the anterior and posterior Clare-Bishop cortex of the cat.

Authors:  K Toyama; K Fujii; K Umetani
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

3.  Visual receptive fields in the lateral suprasylvian area (Clare-Bishop area) of the cat.

Authors:  R Camarda; G Rizzolatti
Journal:  Brain Res       Date:  1976-01-23       Impact factor: 3.252

4.  Receptive-field characteristics of single neurons in lateral suprasylvian visual area of the cat.

Authors:  P D Spear; T P Baumann
Journal:  J Neurophysiol       Date:  1975-11       Impact factor: 2.714

5.  Afferent bases of spatial- and temporal-frequency processing by neurons in the cat's posteromedial lateral suprasylvian cortex: effects of removing areas 17, 18, and 19.

Authors:  W Guido; L Tong; P D Spear
Journal:  J Neurophysiol       Date:  1990-11       Impact factor: 2.714

6.  Spatial and temporal selectivity in the suprasylvian visual cortex of the cat.

Authors:  T J Zumbroich; C Blakemore
Journal:  J Neurosci       Date:  1987-02       Impact factor: 6.167

7.  The responsiveness of Clare-Bishop neurons to size cues for motion stereopsis.

Authors:  K Toyama; K Fujii; S Kasai; K Maeda
Journal:  Neurosci Res       Date:  1986-12       Impact factor: 3.304

8.  Spatial and temporal properties of neurons of the lateral suprasylvian cortex of the cat.

Authors:  M C Morrone; M Di Stefano; D C Burr
Journal:  J Neurophysiol       Date:  1986-10       Impact factor: 2.714

9.  Corticocortical connections among visual areas in the cat.

Authors:  L L Symonds; A C Rosenquist
Journal:  J Comp Neurol       Date:  1984-10-10       Impact factor: 3.215

10.  The anatomical organization of the suprasylvian gyrus of the cat.

Authors:  C J Heath; E G Jones
Journal:  Ergeb Anat Entwicklungsgesch       Date:  1971
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  6 in total

1.  Functional biases in visual cortex neurons with identified projections to higher cortical targets.

Authors:  Beata Jarosiewicz; James Schummers; Wasim Q Malik; Emery N Brown; Mriganka Sur
Journal:  Curr Biol       Date:  2012-02-02       Impact factor: 10.834

2.  Binocular interactions and disparity coding in area 21a of cat extrastriate visual cortex.

Authors:  C Wang; B Dreher
Journal:  Exp Brain Res       Date:  1996-03       Impact factor: 1.972

3.  Spatial and temporal frequency selectivity of cells in area 21a of the cat.

Authors:  J W Morley; R M Vickery
Journal:  J Physiol       Date:  1997-06-01       Impact factor: 5.182

4.  Deficits of visual motion perception and optokinetic nystagmus after posterior suprasylvian lesions in the ferret (Mustela putorius furo).

Authors:  D Hupfeld; C Distler; K-P Hoffmann
Journal:  Exp Brain Res       Date:  2007-06-26       Impact factor: 1.972

Review 5.  Visual pathways serving motion detection in the mammalian brain.

Authors:  Alice Rokszin; Zita Márkus; Gábor Braunitzer; Antal Berényi; György Benedek; Attila Nagy
Journal:  Sensors (Basel)       Date:  2010-04-01       Impact factor: 3.576

6.  Target dependence of orientation and direction selectivity of corticocortical projection neurons in the mouse V1.

Authors:  Teppei Matsui; Kenichi Ohki
Journal:  Front Neural Circuits       Date:  2013-09-23       Impact factor: 3.492

  6 in total

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