Literature DB >> 8158236

Length and width tuning of neurons in the cat's primary visual cortex.

G C DeAngelis1, R D Freeman, I Ohzawa.   

Abstract

1. The classically defined receptive field of a visual neuron is the area of visual space over which the cell responds to visual stimuli. It is well established, however, that the discharge produced by an optimal stimulus can be modulated by the presence of additional stimuli that by themselves do not produce any response. This study examines inhibitory influences that originate from areas located outside of the classical (i.e., excitatory) receptive field. Previous work has shown that for some cells the response to a properly oriented bar of light becomes attenuated when the bar extends beyond the receptive field, a phenomenon known as end-inhibition (or length tuning). Analogously, it has been shown that increasing the number of cycles of a drifting grating stimulus may also inhibit the firing of some cells, an effect known as side-inhibition (or width tuning). Very little information is available, however, about the relationship between end- and side-inhibition. We have examined the spatial organization and tuning characteristics of these inhibitory effects by recording extracellularly from single neurons in the cat's striate cortex (Area 17). 2. For each cortical neuron, length and width tuning curves were obtained with the use of rectangular patches of drifting sinusoidal gratings that have variable length and width. Results from 82 cells show that the strengths of end- and side-inhibition tend to be correlated. Most cells that exhibit clear end-inhibition also show a similar degree of side-inhibition. For these cells, the excitatory receptive field is surrounded on all sides by inhibitory zones. Some cells exhibit only end- or side-inhibition, but not both. Data for 28 binocular cells show that length and width tuning curves for the dominant and nondominant eyes tend to be closely matched. 3. We also measured tuning characteristics of end- and side-inhibition. To obtain these data, the excitatory receptive field was stimulated with a grating patch having optimal orientation, spatial frequency, and size, whereas the end- or side-inhibitory regions were stimulated with patches of gratings that had a variable parameter (such as orientation). Results show that end- and side-inhibition tend to be strongest at the orientation and spatial frequency that yield maximal excitation. However, orientation and spatial frequency tuning curves for inhibition are considerably broader than those for excitation, suggesting that inhibition is mediated by a pool of neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1994        PMID: 8158236     DOI: 10.1152/jn.1994.71.1.347

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


  154 in total

1.  Asymmetric suppression outside the classical receptive field of the visual cortex.

Authors:  G A Walker; I Ohzawa; R D Freeman
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Spatial summation in lateral geniculate nucleus and visual cortex.

Authors:  H E Jones; I M Andolina; N M Oakely; P C Murphy; A M Sillito
Journal:  Exp Brain Res       Date:  2000-11       Impact factor: 1.972

3.  Contrast gain control in the visual cortex: monocular versus binocular mechanisms.

Authors:  A M Truchard; I Ohzawa; R D Freeman
Journal:  J Neurosci       Date:  2000-04-15       Impact factor: 6.167

4.  Membrane potential and conductance changes underlying length tuning of cells in cat primary visual cortex.

Authors:  J S Anderson; I Lampl; D C Gillespie; D Ferster
Journal:  J Neurosci       Date:  2001-03-15       Impact factor: 6.167

5.  Dynamics of spatial frequency tuning in macaque V1.

Authors:  C E Bredfeldt; D L Ringach
Journal:  J Neurosci       Date:  2002-03-01       Impact factor: 6.167

6.  Oriented axon projections in primary visual cortex of the monkey.

Authors:  L C Sincich; G G Blasdel
Journal:  J Neurosci       Date:  2001-06-15       Impact factor: 6.167

7.  The disinhibitory zone of the striate neuron receptive field and its sensitivity to cross-like figures.

Authors:  N A Lazareva; I A Shevelev; R V Novikova; A S Tikhomirov; G A Sharaev; D Yu Tsutskiridze
Journal:  Neurosci Behav Physiol       Date:  2002 Nov-Dec

8.  Circuits for local and global signal integration in primary visual cortex.

Authors:  Alessandra Angelucci; Jonathan B Levitt; Emma J S Walton; Jean-Michel Hupe; Jean Bullier; Jennifer S Lund
Journal:  J Neurosci       Date:  2002-10-01       Impact factor: 6.167

9.  Response suppression in v1 agrees with psychophysics of surround masking.

Authors:  Barbara Zenger-Landolt; David J Heeger
Journal:  J Neurosci       Date:  2003-07-30       Impact factor: 6.167

10.  Signals in macaque striate cortical neurons that support the perception of glass patterns.

Authors:  Matthew A Smith; Wyeth Bair; J Anthony Movshon
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

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