JN Information on EB 2010
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 92: 1708-1717, 2004. First published May 5, 2004; doi:10.1152/jn.00176.2004
0022-3077/04 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
92/3/1708    most recent
00176.2004v1
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 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 Web of Science (20)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nolt, M. J.
Right arrow Articles by Palmer, L. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nolt, M. J.
Right arrow Articles by Palmer, L. A.

Contrast-Dependent Spatial Summation in the Lateral Geniculate Nucleus and Retina of the Cat

M. J. Nolt, R. D. Kumbhani and L. A. Palmer

Department of Neuroscience, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104

Submitted 25 February 2004; accepted in final form 27 April 2004

Based on extracellular recordings from 69 lateral geniculate nucleus (LGN) cells in the anesthetized cat, we found spatial summation within their receptive fields to be dependent on the contrast of the stimuli presented. By fitting the summation curves to a difference of Gaussians model, we attributed this contrast-dependent effect to an actual change in the size of the center mechanism. Analogous changes in spatial frequency tuning were also observed, specifically increased peaks and cut-off frequencies with contrast. These effects were seen across the populations of both X and Y cell types. In a few cases, LGN cells were recorded simultaneously with one of their retinal ganglion cell (RGC) inputs (S-potentials). In every case, the RGCs exhibited similar contrast-dependent effects in the space and spatial-frequency domains. We propose that this contrast dependency in the retinal ganglion cells results directly from a reduction in the size of the center mechanism due to an increase in contrast. We also propose that these properties first arise in the retina and are transmitted passively through the LGN to visual cortex.


Address for reprint requests and other correspondence: M. J. Nolt, 215 Stemmler Hall, Dept. of Neuroscience, School of Medicine, Univ. of Pennsylvania, Philadelphia, PA 19104-6060 (E-mail: nolt{at}mail.med.upenn.edu).




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
C.-I Yeh, C. R. Stoelzel, C. Weng, and J.-M. Alonso
Functional Consequences of Neuronal Divergence Within the Retinogeniculate Pathway
J Neurophysiol, April 1, 2009; 101(4): 2166 - 2185.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. L. Passaglia, D. K. Freeman, and J. B. Troy
Effects of Remote Stimulation on the Modulated Activity of Cat Retinal Ganglion Cells
J. Neurosci., February 25, 2009; 29(8): 2467 - 2476.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Wielaard and P. Sajda
Dependence of Response Properties on Sparse Connectivity in a Spiking Neuron Model of the Lateral Geniculate Nucleus
J Neurophysiol, December 1, 2007; 98(6): 3292 - 3308.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. D. Kumbhani, M. J. Nolt, and L. A. Palmer
Precision, Reliability, and Information-Theoretic Analysis of Visual Thalamocortical Neurons
J Neurophysiol, November 1, 2007; 98(5): 2647 - 2663.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. M. Ichida, L. Schwabe, P. C. Bressloff, and A. Angelucci
Response Facilitation From the "Suppressive" Receptive Field Surround of Macaque V1 Neurons
J Neurophysiol, October 1, 2007; 98(4): 2168 - 2181.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. J. Nolt, R. D. Kumbhani, and L. A. Palmer
Suppression at High Spatial Frequencies in the Lateral Geniculate Nucleus of the Cat
J Neurophysiol, September 1, 2007; 98(3): 1167 - 1180.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. L. Rathbun, H. J. Alitto, T. G. Weyand, and W. M. Usrey
Interspike Interval Analysis of Retinal Ganglion Cell Receptive Fields
J Neurophysiol, August 1, 2007; 98(2): 911 - 919.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. P. Sceniak, S. Chatterjee, and E. M. Callaway
Visual Spatial Summation in Macaque Geniculocortical Afferents
J Neurophysiol, December 1, 2006; 96(6): 3474 - 3484.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. R. Peterson, B. Li, and R. D. Freeman
Direction Selectivity of Neurons in the Striate Cortex Increases as Stimulus Contrast Is Decreased
J Neurophysiol, April 1, 2006; 95(4): 2705 - 2712.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
V. Bonin, V. Mante, and M. Carandini
The Suppressive Field of Neurons in Lateral Geniculate Nucleus
J. Neurosci., November 23, 2005; 25(47): 10844 - 10856.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the The American Physiological Society.