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


     


J Neurophysiol 38: 1080-1098, 1975;
0022-3077/75 $5.00
This Article
Right arrow Full Text (PDF)
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 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 Google Scholar
Google Scholar
Right arrow Articles by Singer, W.
Right arrow Articles by Cynader, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Singer, W.
Right arrow Articles by Cynader, M.

Journal of Neurophysiology, Vol 38, Issue 5 1080-1098, Copyright © 1975 by APS


ARTICLES

Organization of cat striate cortex: a correlation of receptive-field properties with afferent and efferent connections

W. Singer, F. Tretter and M. Cynader

The purposes of this study were 1) to relate the receptive-field characteristics of area 17 cells to their afferent and efferent connections, and 2) to obtain quantitative data from area 17 neurons for later comparison with area 18 cells. Intra- and extracellular recordings were obtained in paralyzed preparations which were anesthetized with nitrous oxide. The connectivities of the recorded cells were determined from responses to electrical stimulation of afferent and efferent pathways. In parallel to the classification of units as simple and complex cells, the receptive fields were grouped in four classes according to the spatial arrangement of on- and off-areas; class I, fields with exclusive on- or off-areas; class II, fields with spatially separate on- and off-areas; class III, fields with mixed on-off areas; class IV, fields which could not be mapped with stationary stimuli. The results from electrical stimulation suggest two major classes of cells: cells in the first group are driven mainly or exclusively by LGN afferents. They rarely receive additional excitation from intrinsic or callosal afferents and rarely possess corticofugal axons. Cells in the second group receive either converging inputs from LGN afferents and further intrinsic afferents or only from intrinsic afferents. They frequently received additional input from callosum and from recurrent collaterals of corticofugal axons. They project subcortically more often than cells in the first group. Cells in both groups can be driven either by X- or Y-type afferents. Cells in the first group have mainly class I and class II fields or simple fields, whereas the neurons in the second group have mainly class III and class IV fields or complex fields. Thus, simple and complex cells differ in their connectivity patterns, but the discriminative parameter is neither the selective connection to the X- or the Y-system nor, in a strict sense, the synaptic distance from subcortical input. From the combined consideration of receptive-field properties and connectivity patterns it is concluded that class I and class II cells or simple cells are concerned mainly with the primary analysis of subcortical activity, whereas class III and class IV cells or complex cells perform a correlative analysis between highly convergent activity from extrinsic and intrinsic afferents.


This article has been cited by other articles:


Home page
Cereb CortexHome page
L. G. Nowak, M. V. Sanchez-Vives, and D. A. McCormick
Lack of Orientation and Direction Selectivity in a Subgroup of Fast-Spiking Inhibitory Interneurons: Cellular and Synaptic Mechanisms and Comparison with Other Electrophysiological Cell Types
Cereb Cortex, May 1, 2008; 18(5): 1058 - 1078.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. Bardy, J. Y. Huang, C. Wang, T. FitzGibbon, and B. Dreher
'Simplification' of responses of complex cells in cat striate cortex: suppressive surrounds and 'feedback' inactivation
J. Physiol., August 1, 2006; 574(3): 731 - 750.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. A. Sommer and R. H. Wurtz
What the Brain Stem Tells the Frontal Cortex. I. Oculomotor Signals Sent From Superior Colliculus to Frontal Eye Field Via Mediodorsal Thalamus
J Neurophysiol, March 1, 2004; 91(3): 1381 - 1402.
[Abstract] [Full Text] [PDF]


Home page
NeuroscientistHome page
L. M. Martinez and J.-M. Alonso
Complex Receptive Fields in Primary Visual Cortex
Neuroscientist, October 1, 2003; 9(5): 317 - 331.
[Abstract] [PDF]


Home page
J. Neurosci.Home page
M. Castelo-Branco, S. Neuenschwander, and W. Singer
Synchronization of Visual Responses between the Cortex, Lateral Geniculate Nucleus, and Retina in the Anesthetized Cat
J. Neurosci., August 15, 1998; 18(16): 6395 - 6410.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
B. Breitmeyer and A Valberg
Local foveal inhibitory effects of global peripheral excitation
Science, February 2, 1979; 203(4379): 463 - 464.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online