The extrafoveal retina if the human eye contains both rod and cone photoreceptor systems. Once thought to function independently, rod and cone systems have been shown in recent years to interact under many experimental conditions. However, the role of these rod-cone interactions in human vision is not well understood. Interactions between rods and cones become of particular importance in ocular disorders such as retinitis pigmentosa and cone dystophy, in which visual losses in the peripheral field may be due only to alterations within rod or cone mechanisms, but also to abnormalities in rod-cone interactions. The research proposed in this application will investigate the properties of an unusual type of rod-cone interaction that has recently been discovered. Experiments have shown that in the dark-adapted eye, the unstimulated rods surrounding a flickering test stimulus substantially reduce the flicker sensitivity of the cone system at high temporal frequencies.
The specific aims of the research are first, to measure the spatial and chromatic properties of this rod-cone flicker interaction in normal individuals; second, to determine whether the interaction is abnormal in certain types of color vision deficiencies, as suggested by preliminary studies; and third, to determine the locus of the interaction within the visual system by studying the interaction in selected patients with visual disorders in which the underlying pathological changes are known to occur at specific levels of the visual system. Flicker sensitivity will be measured using either a Maxwellian-view optical system (normal subjects) or a Tubinger perimeter (color deficient subjects amd patients with visual disorders). The long-term objective is to determine the mechanisms by which rods and cones interact in the detection of flicker in the normal human visual system. If the mechanism underlying peripheral flicker detection can be identified, then abnormalities in flicker detection, such as these that have been observed in patients with ocular disorders, will provide useful information concerning the pathological changes that accompany these disorders.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004848-02
Application #
3259380
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1984-08-01
Project End
1987-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Peachey, N S; Alexander, K R; Derlacki, D J (1990) Spatial properties of rod-cone interactions in flicker and hue detection. Vision Res 30:1205-10
Peachey, N S; Alexander, K R; Fishman, G A (1989) The luminance-response function of the dark-adapted human electroretinogram. Vision Res 29:263-70
Kilbride, P E; Alexander, K R; Fishman, M et al. (1989) Human macular pigment assessed by imaging fundus reflectometry. Vision Res 29:663-74
Peachey, N S; Fishman, G A; Derlacki, D J et al. (1988) Rod and cone dysfunction in carriers of X-linked retinitis pigmentosa. Ophthalmology 95:677-85
Alexander, K R; Fishman, G A; Derlacki, D J (1988) Mechanisms of rod-cone interaction: evidence from congenital stationary nightblindness. Vision Res 28:575-83
Alexander, K R; Hutman, L P; Fishman, G A (1987) Abnormal foveal spectral sensitivity in retinitis pigmentosa. Invest Ophthalmol Vis Sci 28:725-30
Alexander, K R; Kilbride, P E; Fishman, G A et al. (1987) Macular pigment and reduced foveal short-wavelength sensitivity in retinitis pigmentosa. Vision Res 27:1077-83
Peachey, N S; Alexander, K R; Fishman, G A (1987) Rod and cone system contributions to oscillatory potentials: an explanation for the conditioning flash effect. Vision Res 27:859-66
Alexander, K R; Kelly, S A; Morris, M A (1986) Background size and saturation of the rod system. Vision Res 26:299-312
Alexander, K R; Hutman, L P; Fishman, G A (1986) Dark-adapted foveal thresholds and visual acuity in retinitis pigmentosa. Arch Ophthalmol 104:390-4

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