Literature DB >> 9151419

Parallel processing by a homogeneous group of coupled model neurons can enhance, reduce and generate signal correlations.

E Juergens1, R Eckhorn.   

Abstract

Correlated activities have been proposed as correlates of flexible association and assembly coding. We addressed the basic question of how signal correlations on parallel pathways are enhanced, reduced and generated by homogeneous groups of coupled neurons, and how this depends on the input activities and their interactions with internal coupling processes. For this we simulated a fully connected group of identical impulse-coded neurons with dynamic input and threshold processes and additive or multiplicative lateral coupling. Input signals were Gaussian white noise (GWN), completely independent or partially correlated on a subgroup of the parallel inputs. We show that in states of high average spike rates input-output correlations were weak while the network could generate correlated activities of stochastic, oscillatory and rhythmic bursting types depending exclusively on lateral coupling strength. In states of low average spike rates input-output correlations were high and the network could effectively enhance or reduce differences in spatial correlation applied to its parallel inputs. The correlation differences were more pronounced with multiplicative lateral coupling than with the additive interactions commonly used. As the different modes of correlation processing emerged already by global changes in the average spike rate and lateral coupling strength, we assume that in real cortical circuits changes in correlational processing may also be induced by unspecific modulations of activation and lateral coupling.

Mesh:

Year:  1997        PMID: 9151419     DOI: 10.1007/s004220050334

Source DB:  PubMed          Journal:  Biol Cybern        ISSN: 0340-1200            Impact factor:   2.086


  7 in total

1.  Neuronal interactions improve cortical population coding of movement direction.

Authors:  E M Maynard; N G Hatsopoulos; C L Ojakangas; B D Acuna; J N Sanes; R A Normann; J P Donoghue
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

2.  Coding specificity in cortical microcircuits: a multiple-electrode analysis of primate prefrontal cortex.

Authors:  C Constantinidis; M N Franowicz; P S Goldman-Rakic
Journal:  J Neurosci       Date:  2001-05-15       Impact factor: 6.167

3.  Rich-Club Organization in Effective Connectivity among Cortical Neurons.

Authors:  Sunny Nigam; Masanori Shimono; Shinya Ito; Fang-Chin Yeh; Nicholas Timme; Maxym Myroshnychenko; Christopher C Lapish; Zachary Tosi; Pawel Hottowy; Wesley C Smith; Sotiris C Masmanidis; Alan M Litke; Olaf Sporns; John M Beggs
Journal:  J Neurosci       Date:  2016-01-20       Impact factor: 6.167

4.  Information about movement direction obtained from synchronous activity of motor cortical neurons.

Authors:  N G Hatsopoulos; C L Ojakangas; L Paninski; J P Donoghue
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

5.  Modulation dynamics in the orofacial sensorimotor cortex during motor skill acquisition.

Authors:  Fritzie I Arce-McShane; Nicholas G Hatsopoulos; Jye-Chang Lee; Callum F Ross; Barry J Sessle
Journal:  J Neurosci       Date:  2014-04-23       Impact factor: 6.167

6.  Extending transfer entropy improves identification of effective connectivity in a spiking cortical network model.

Authors:  Shinya Ito; Michael E Hansen; Randy Heiland; Andrew Lumsdaine; Alan M Litke; John M Beggs
Journal:  PLoS One       Date:  2011-11-15       Impact factor: 3.240

7.  Functional Clusters, Hubs, and Communities in the Cortical Microconnectome.

Authors:  Masanori Shimono; John M Beggs
Journal:  Cereb Cortex       Date:  2014-10-21       Impact factor: 5.357

  7 in total

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