The principal aims of this project are to integrate information from the spatial, temporal, directional and binocular domains, derived from responses to achromatic stimuli, into physiologically based descriptions of V1 receptive fields (r.f.'s) and to use this multidimensional assessment to characterize neurons within the different layers and sublayers of V1. It is also proposed to extend the difference of Gaussians based spatial model of r.f. structure to include temporal parameters. In initial experiments the spatial, spatial frequency and orientation tuning of V1 neurons will be measured over a range of temporal modulations of the stimulus. A full spatiotemporal tuning function will be obtained for each neuron using a threshold tracking method. In addition, response- contrast functions will be measured at selected points over the spatiotemporal surface to obtain estimates of the contrast gain and the extent of the compressive contrast non-linearity. In a second series of experiments, monocular and binocular tuning will be measured and compared, using sinewave grating stimuli. Dichoptic presentation will be used to determine binocular interaction at different spatial phases, spatial frequencies and contrasts. In some experiments, disparity sensitivity will be measured. The third part of this proposal is to apply the detailed quantitative measures in the spatial, temporal and binocular domains to categorize cells and determine the distribution of the functional classes both within and across different cortical layers. It is intended to concentrate on the major output layers, layers 2 + 3, 4b, 5 and 6 all of which have distinct extrastriate or sub-cortical targets. These experiments will give a comprehensive description of the properties of the neurons providing afferent input to specific extrastroate areas and therefore the limits of information available to these areas from V1. The relationship between r.f. size and eccentricity will be investigated along with the underlying density of cone photoreceptors.
The aim i s to obtain measures of local spatial scale as well as to examine whether any differences in local spatial scale, particularly in the foveal region, can be related to the cone distribution. In many forms of amblyopia there is a severe disruption of performance on spatial and binocular tasks, and it is thought that the primary neural locus of the disfunction is the striate cortex. The multidimensional quantitative description of r.f. properties will be important in defining the expected limits of performance of different cell types in different layers in V1 of the adult macaque and is therefore basic to the understanding and treatment of the developmental disorders affecting the central visual pathways.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY008300-03
Application #
3265575
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1990-05-01
Project End
1995-04-30
Budget Start
1992-05-01
Budget End
1993-04-30
Support Year
3
Fiscal Year
1992
Total Cost
Indirect Cost
Name
New York University
Department
Type
Schools of Arts and Sciences
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
Henry, Christopher A; Joshi, Siddhartha; Xing, Dajun et al. (2013) Functional characterization of the extraclassical receptive field in macaque V1: contrast, orientation, and temporal dynamics. J Neurosci 33:6230-42
Henry, Christopher A; Hawken, Michael J (2013) Stability of simple/complex classification with contrast and extraclassical receptive field modulation in macaque V1. J Neurophysiol 109:1793-803
Disney, Anita A; Aoki, Chiye; Hawken, Michael J (2012) Cholinergic suppression of visual responses in primate V1 is mediated by GABAergic inhibition. J Neurophysiol 108:1907-23
Lee, Barry B; Shapley, Robert M; Hawken, Michael J et al. (2012) Spatial distributions of cone inputs to cells of the parvocellular pathway investigated with cone-isolating gratings. J Opt Soc Am A Opt Image Sci Vis 29:A223-32
Xing, Dajun; Ringach, Dario L; Hawken, Michael J et al. (2011) Untuned suppression makes a major contribution to the enhancement of orientation selectivity in macaque v1. J Neurosci 31:15972-82
Shapley, Robert; Hawken, Michael J (2011) Color in the cortex: single- and double-opponent cells. Vision Res 51:701-17
Constantinople, Christine M; Disney, Anita A; Maffie, Jonathan et al. (2009) Quantitative analysis of neurons with Kv3 potassium channel subunits, Kv3.1b and Kv3.2, in macaque primary visual cortex. J Comp Neurol 516:291-311
Johnson, Elizabeth N; Hawken, Michael J; Shapley, Robert (2008) The orientation selectivity of color-responsive neurons in macaque V1. J Neurosci 28:8096-106
Henrie, J Andrew; Shapley, Robert (2005) LFP power spectra in V1 cortex: the graded effect of stimulus contrast. J Neurophysiol 94:479-90
Mareschal, I; Sceniak, M P; Shapley, R M (2001) Contextual influences on orientation discrimination: binding local and global cues. Vision Res 41:1915-30

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