Literature DB >> 12106294

Stimulus-Dependent Neuronal Oscillations in Cat Visual Cortex: Inter-Columnar Interaction as Determined by Cross-Correlation Analysis.

Andreas K. Engel1, Peter König, Charles M. Gray, Wolf Singer.   

Abstract

We have demonstrated previously that neurons in cat striate cortex, in response to their preferred stimuli, exhibit oscillatory responses in a frequency range of 40 - 60 Hz. Recently, we obtained evidence that such oscillatory responses can synchronize across columns. We have now performed an extensive analysis of this phenomenon for both unit and field potential responses. In addition, we studied the stimulus conditions leading to intercolumnar synchronization. We recorded both multi-unit activity and local field potentials from area 17 of adult cats with arrays of several electrodes. Interelectrode distances ranged from 0.4 to 12 mm. For all pairs of unit (n=200) and field potential (n=174) recordings, we computed auto- and cross-correlation functions. The modulation of the correlograms was quantified by fitting a damped sine wave (Gabor) function to the data. Cross-correlation analysis of the unit data revealed that in 90 out of 200 cases the recorded cells established a constant phase-relationship of their oscillatory responses. This occurred, on average, with no phase difference. If the receptive fields were nonoverlapping, we observed a synchronization primarily between cells with similar orientation preferences. Cells with overlapping receptive fields also showed a high incidence of synchronization if their orientation preferences were different. In this latter group, synchronization occurred even in cases where the stimulus was optimal for only one of the recording sites. Under conditions of monocular instead of binocular stimulation the oscillatory modulation of the responses was attenuated, but the cross-correlogram still indicated a significant interaction. Similar effects were seen with the application of stationary instead of moving stimuli. A synchronization of oscillatory field potential responses was observed in 136 out of 174 paired recordings. At all distances investigated, the probability of synchronization of field potential responses was independent of the orientation preferences of the cells. However, the strength of interaction decreased with increasing spatial separation. Control experiments showed that the synchronization of field potential responses was not due to volume conduction. The results demonstrate that oscillatory responses at separate cortical sites can transiently synchronize. The probability and strength of synchronization are dependent on the spatial separation of the recorded cells and their orientation preferences. In addition, the cross-columnar synchronization is influenced by features of the visual stimulus. It is suggested that this synchronization provides a mechanism for the formation of neuronal assemblies in the visual cortex.

Entities:  

Year:  1990        PMID: 12106294     DOI: 10.1111/j.1460-9568.1990.tb00449.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  78 in total

1.  Top-down processing mediated by interareal synchronization.

Authors:  A von Stein; C Chiang; P König
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

2.  Analysis of the dynamics of interneuronal functional connections during conditioned reflex activity.

Authors:  A P Kozlov; V V Shabaev
Journal:  Neurosci Behav Physiol       Date:  2000 Nov-Dec

3.  Long-range cortical synchronization without concomitant oscillations in the somatosensory system of anesthetized cats.

Authors:  S A Roy; S P Dear; K D Alloway
Journal:  J Neurosci       Date:  2001-03-01       Impact factor: 6.167

4.  Emergent oscillations in a realistic network: the role of inhibition and the effect of the spatiotemporal distribution of the input.

Authors:  Q Pauluis; S N Baker; E Olivier
Journal:  J Comput Neurosci       Date:  1999-01       Impact factor: 1.621

5.  Patterns of synchronization in the superior colliculus of anesthetized cats.

Authors:  M Brecht; W Singer; A K Engel
Journal:  J Neurosci       Date:  1999-05-01       Impact factor: 6.167

6.  Precisely synchronized oscillatory firing patterns require electroencephalographic activation.

Authors:  S Herculano-Houzel; M H Munk; S Neuenschwander; W Singer
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

7.  Precise burst synchrony in the superior colliculus of the awake cat during moving stimulus presentation.

Authors:  Q Pauluis; S N Baker; E Olivier
Journal:  J Neurosci       Date:  2001-01-15       Impact factor: 6.167

Review 8.  Target and temporal pattern selection at neocortical synapses.

Authors:  Alex M Thomson; A Peter Bannister; Audrey Mercer; Oliver T Morris
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

9.  Towards the cortical representation of form and motion stimuli generated by a retina implant.

Authors:  Thomas Schanze; Nina Greve; Lutz Hesse
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2003-07-29       Impact factor: 3.117

10.  'Gamma' band oscillatory response to chromatic stimuli in volunteers and patients with idiopathic Parkinson's disease.

Authors:  Walter G Sannita; Simone Carozzo; Paolo Orsini; Luciano Domenici; Vittorio Porciatti; Mauro Fioretto; Sergio Garbarino; Ferdinando Sartucci
Journal:  Vision Res       Date:  2009-02-14       Impact factor: 1.886

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