JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 90: 1115-1123, 2003. First published April 17, 2003; doi:10.1152/jn.00480.2002
0022-3077/03 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
90/2/1115    most recent
00480.2002v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (16)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nase, G.
Right arrow Articles by Engel, A. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nase, G.
Right arrow Articles by Engel, A. K.

Features of Neuronal Synchrony in Mouse Visual Cortex

Gabriele Nase1, Wolf Singer1, Hannah Monyer2 and Andreas K. Engel3

1 Abteilung Neurophysiologie, Max-Planck-Institut für Hirnforschung, 60528 Frankfurt; 2 Abt. Klinische Neurobiologie, Universität Heidelberg, 69120 Heidelberg; 3 Institut für Neurophysiologie und Pathophysiologie, Universitätsklinikum Hamburg-Eppendorf, 20246 Hamburg, Germany

Submitted 1 July 2002; accepted in final form 31 March 2003

Synchronization of neuronal discharges has been hypothesized to play a role in defining cell assemblies representing particular constellations of stimulus features. In many systems and species, synchronization is accompanied by an oscillatory response modulation at frequencies in the {gamma}-band. The cellular mechanisms underlying these phenomena of synchronization and oscillatory patterning have been studied mainly in vitro due to the difficulty in designing a direct in vivo assay. With the prospect of using conditional genetic manipulations of cortical network components, our objective was to test whether the mouse would meet the criteria to provide a model system for the study of {gamma}-band synchrony. Multi-unit and local field potential recordings were made from the primary visual cortex of anesthetized C57BL/6J mice. Neuronal responses evoked by moving gratings, bars, and random dot patterns were analyzed with respect to neuronal synchrony and temporal patterning. Oscillations at {gamma}-frequencies were readily evoked with all types of stimuli used. Oscillation and synchronization strength were largest for gratings and decreased when the noise level was increased in random-dot patterns. The center peak width of cross-correlograms was smallest for bars and increased with noise, yielding a significant difference between coherent random dot patterns versus patterns with 70% noise. Field potential analysis typically revealed increases of power in the {gamma}-band during response periods. Our findings are compatible with a role for neuronal synchrony in mediating perceptual binding and suggest the usefulness of the mouse model for testing hypotheses concerning both the mechanisms and the functional role of temporal patterning.


Address for reprint requests: G. Nase, Abt. Neurophysiologie, Max-Planck-Institut für Hirnforschung, Deutschordenstr. 46, 60528 Frankfurt, Germany (E-mail: nase{at}mpih-frankfurt.mpg.de).




This article has been cited by other articles:


Home page
Schizophr BullHome page
P. J. Uhlhaas, C. Haenschel, D. Nikolic, and W. Singer
The Role of Oscillations and Synchrony in Cortical Networks and Their Putative Relevance for the Pathophysiology of Schizophrenia
Schizophr Bull, September 1, 2008; 34(5): 927 - 943.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. M. Niell and M. P. Stryker
Highly Selective Receptive Fields in Mouse Visual Cortex
J. Neurosci., July 23, 2008; 28(30): 7520 - 7536.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Tsanov and D. Manahan-Vaughan
Intrinsic, Light-Independent and Visual Activity-Dependent Mechanisms Cooperate in the Shaping of the Field Response in Rat Visual Cortex
J. Neurosci., August 1, 2007; 27(31): 8422 - 8429.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. G. Knyazeva, E. Fornari, R. Meuli, and P. Maeder
Interhemispheric Integration at Different Spatial Scales: The Evidence From EEG Coherence and fMRI
J Neurophysiol, July 1, 2006; 96(1): 259 - 275.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. S. Sohal and J. R. Huguenard
Inhibitory coupling specifically generates emergent gamma oscillations in diverse cell types
PNAS, December 20, 2005; 102(51): 18638 - 18643.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. M. Samonds and A. B. Bonds
Gamma Oscillation Maintains Stimulus Structure-Dependent Synchronization in Cat Visual Cortex
J Neurophysiol, January 1, 2005; 93(1): 223 - 236.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
V. Wespatat, F. Tennigkeit, and W. Singer
Phase Sensitivity of Synaptic Modifications in Oscillating Cells of Rat Visual Cortex
J. Neurosci., October 13, 2004; 24(41): 9067 - 9075.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2003 by the The American Physiological Society.