JN AJP: Advances in Physiology Education
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


J Neurophysiol (May 11, 2005). doi:10.1152/jn.00826.2004
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
94/3/1789    most recent
00826.2004v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 (13)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Webb, B. S
Right arrow Articles by Derrington, A. M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Webb, B. S
Right arrow Articles by Derrington, A. M
Submitted on August 12, 2004
Accepted on May 10, 2005

Spatial Distribution of Suppressive Signals Outside the Classical Receptive-Field in Lateral Geniculate Nucleus

Ben S Webb1*, Christopher J Tinsley1, Christopher J Vincent1, and Andrew M Derrington1

1 School of Psychology, University of Nottingham, Nottingham, United Kingdom

* To whom correspondence should be addressed. E-mail: bsw{at}psychology.nottingham.ac.uk.

A suppressive surround modulates the responsiveness of cells in the lateral geniculate nucleus (LGN), but we know nothing of its spatial structure or the way in which it combines signals arising from different locations. It is generally assumed that suppressive signals are either uniformly distributed or balanced in opposing regions outside the receptive field. Here, we examine the spatial distribution and summation of suppressive signals outside the receptive-field in extracellular recordings from 46 LGN cells in anaesthetized marmosets. The receptive-field of each cell was stimulated with a drifting sinusoidal grating of the preferred size and spatial- and temporal-frequency; we probed different positions in the suppressive surround with either a large half-annular grating or a small circular grating patch of the preferred spatial-and temporal-frequency. In many of the cells with a strong suppressive surround (29/46), the spatial distribution of suppression showed clear deviation from circular symmetry. In the majority of these of cells, suppressive signals were spatially asymmetrical or balanced in opposing areas outside the receptive-field. A suppressive area was larger than the classical receptive-field itself and spatial summation within and between these areas was non-linear. There was no bias for suppression to arise from foveal or nasal retina where cone density is higher, and no other sign of a systematic spatial organization to the suppressive surround. We conclude that non-classical suppressive signals in LGN deviate from circular symmetry and are non-linearly combined.




This article has been cited by other articles:


Home page
J. Neurosci.Home page
A. J. Camp, C. Tailby, and S. G. Solomon
Adaptable Mechanisms That Regulate the Contrast Response of Neurons in the Primate Lateral Geniculate Nucleus
J. Neurosci., April 15, 2009; 29(15): 5009 - 5021.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. Tailby, B. A. Szmajda, P. Buzas, B. B. Lee, and P. R. Martin
Transmission of blue (S) cone signals through the primate lateral geniculate nucleus
J. Physiol., December 15, 2008; 586(24): 5947 - 5967.
[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
K. A. Zaghloul, M. B. Manookin, B. G. Borghuis, K. Boahen, and J. B. Demb
Functional Circuitry for Peripheral Suppression in Mammalian Y-Type Retinal Ganglion Cells
J Neurophysiol, June 1, 2007; 97(6): 4327 - 4340.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. J. Higley and D. Contreras
Cellular Mechanisms of Suppressive Interactions Between Somatosensory Responses In Vivo
J Neurophysiol, January 1, 2007; 97(1): 647 - 658.
[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. Neurosci.Home page
S. G. Solomon, B. B. Lee, and H. Sun
Suppressive surrounds and contrast gain in magnocellular-pathway retinal ganglion cells of macaque.
J. Neurosci., August 23, 2006; 26(34): 8715 - 8726.
[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
Visit Other APS Journals Online
Copyright © 2005 by the The American Physiological Society.