Literature DB >> 1992006

Temporal interactions in the cat visual system. II. Suppressive and facilitatory effects in the lateral geniculate nucleus.

S B Nelson1.   

Abstract

Extracellular responses were recorded from single neurons in the lateral geniculate nucleus (LGN) of the cat during presentation of pairs of brief visual stimuli identical to those that produce orientation-selective paired-pulsed suppression in the visual cortex. LGN neurons also show paired-pulse suppression, but the suppression is not orientation selective, and it occurs only for short interstimulus intervals (ISIs; usually less than 200 msec). At longer ISIs, most LGN neurons show a period of facilitation. Thus, the paired-pulse suppression in the LGN cannot account for that seen in the visual cortex. Paired-pulse suppression in the LGN was found to be enhanced by stimulation of the receptive field surround. LGN neurons also showed a second type of suppression, termed "offset suppression," which consisted of a more long-lasting suppression of spontaneous activity following the offset of an excitatory visual stimulus. The suppression of spontaneous activity was accompanied by a reduction of the antidromic excitability, assessed by stimulating LGN axons within the cortex or optic radiation. Unlike paired-pulsed suppression, offset suppression was not enhanced by increased stimulation of the receptive field surround. Paired-pulse suppression and offset suppression are most likely due to different mechanisms because they have different time courses and depend differently on the spatial properties of the stimuli. Functionally, paired-pulse suppression may be related to the reduced visual sensitivity that accompanies eye movements, while offset suppression may serve to enhance temporal contrast.

Mesh:

Year:  1991        PMID: 1992006      PMCID: PMC6575213     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  8 in total

1.  Similar adaptation effects in primary visual cortex and area MT of the macaque monkey under matched stimulus conditions.

Authors:  Carlyn A Patterson; Jacob Duijnhouwer; Stephanie C Wissig; Bart Krekelberg; Adam Kohn
Journal:  J Neurophysiol       Date:  2013-12-26       Impact factor: 2.714

2.  An fMRI study of neural interaction in large-scale cortico-thalamic visual network.

Authors:  Nanyin Zhang; Xiao-Hong Zhu; Yi Zhang; Wei Chen
Journal:  Neuroimage       Date:  2008-06-12       Impact factor: 6.556

3.  Rebounding V1 activity and a new visual aftereffect.

Authors:  Xin Huang; Samuel Levine; Michael A Paradiso
Journal:  J Vis       Date:  2008-03-27       Impact factor: 2.240

4.  Postnatal development of onset transient responses in macaque V1 AND V2 neurons.

Authors:  Bin Zhang; Earl L Smith; Yuzo M Chino
Journal:  J Neurophysiol       Date:  2008-06-25       Impact factor: 2.714

5.  Constraints on the source of short-term motion adaptation in macaque area MT. II. tuning of neural circuit mechanisms.

Authors:  Nicholas J Priebe; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2002-07       Impact factor: 2.714

6.  Synaptic depression and slow oscillatory activity in a biophysical network model of the cerebral cortex.

Authors:  Jose M Benita; Antoni Guillamon; Gustavo Deco; Maria V Sanchez-Vives
Journal:  Front Comput Neurosci       Date:  2012-08-28       Impact factor: 2.380

7.  Modulation of V1 spike response by temporal interval of spatiotemporal stimulus sequence.

Authors:  Taekjun Kim; Hyunggoo R Kim; Kayeon Kim; Choongkil Lee
Journal:  PLoS One       Date:  2012-10-16       Impact factor: 3.240

8.  Visual cells remember earlier applied target: plasticity of orientation selectivity.

Authors:  Narcis Ghisovan; Abdellatif Nemri; Svetlana Shumikhina; Stephane Molotchnikoff
Journal:  PLoS One       Date:  2008-11-10       Impact factor: 3.240

  8 in total

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