The investigators' long-term objective has been to develop a set of noninvasive techniques for studying the physiology of the human retina. The electroretinogram (ERG), the summed activity of the retinal cells, is a noninvasive measure of retinal activity. The ERG has long been used for diagnosing and following the course of retinal diseases. By building upon discoveries made by the retinal physiologist, they have shown that the usefulness of the ERG can be extended. Their initial observation that the leading edge of the rod a-wave could be described by the same models fitted to single receptor recordings has led to numerous studies of normal and abnormal retinal activity in humans and in animal models of retinal diseases. As part of aim 1 (INNER RETINA, MF-ERG), they propose to examine the contribution of the inner retina, which includes amacrine and ganglion cells, to a local measure of retinal activity, the cone multifocal ERG. Glaucoma, one of the leading causes of blindness, affects these cells. Current behavioral and electrophysiological procedures for detecting early signs of retinal damage are less than optimal. The investigators believe that they have found a very promising approach to this problem. The approach includes studies involving: a. monkeys in which inner retinal activity is pharmacologically blocked, b. normal human subjects, c. patients with glaucoma, and d. mathematical and statistical work. During the current grant period, they have developed procedures for measuring the response of the human rod receptor and for studying rod on-bipolars.
Aim 2 (UTILIZE TECHNIQUES DEVELOPED IN CURRENT GRANT PERIOD) is to study the activity of the normal and abnormal human rod on-bipolar with these techniques. Further, they will develop a technique for measuring the waveform of the cone photoreceptor response (that is, deactivation) and will use it to study light adaptation and retinal diseases of the cone system.
A third aim (DEVELOP TECHNIQUES FOR ASSESSING INL ACTIVITY IN NL AND ABN RETINAS) is to develop techniques for assessing inner nuclear layer (INL) activity of normal and abnormal retinas. While knowledge of the rod ERG is approaching the point where a computational model may be feasible, in comparison, less in known about the contributions of the bipolar cells to the human cone ERG. Here the investigators attack this problem with studies involving: a. monkeys in which INL activity is pharmacologically dissected, b. normal human subjects, c. patients with disease of the INL, and d. mathematical work.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY009076-11
Application #
6384631
Study Section
Special Emphasis Panel (ZRG1-VISB (03))
Program Officer
Liberman, Ellen S
Project Start
1991-05-01
Project End
2003-04-30
Budget Start
2001-05-01
Budget End
2002-04-30
Support Year
11
Fiscal Year
2001
Total Cost
$278,488
Indirect Cost
Name
Columbia University (N.Y.)
Department
Psychology
Type
Other Domestic Higher Education
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
Duncker, Tobias; Lee, Winston; Jiang, Fan et al. (2018) ACUTE ZONAL OCCULT OUTER RETINOPATHY: Structural and Functional Analysis Across the Transition Zone Between Healthy and Diseased Retina. Retina 38:118-127
Daiger, Stephen P; Bowne, Sara J; Sullivan, Lori S et al. (2018) Molecular Findings in Families with an Initial Diagnose of Autosomal Dominant Retinitis Pigmentosa (adRP). Adv Exp Med Biol 1074:237-245
Soens, Zachry T; Branch, Justin; Wu, Shijing et al. (2017) Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance. Hum Mutat 38:1521-1533
Jones, Kaylie D; Wheaton, Dianna K; Bowne, Sara J et al. (2017) Next-generation sequencing to solve complex inherited retinal dystrophy: A case series of multiple genes contributing to disease in extended families. Mol Vis 23:470-481
Bennett, Lea D; Klein, Martin; Locke, Kirsten G et al. (2017) Dark-Adapted Chromatic Perimetry for Measuring Rod Visual Fields in Patients with Retinitis Pigmentosa. Transl Vis Sci Technol 6:15
Greenstein, Vivienne C; Nunez, Jason; Lee, Winston et al. (2017) A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt Disease. Invest Ophthalmol Vis Sci 58:5227-5236
Verdina, Tommaso; Greenstein, Vivienne C; Sodi, Andrea et al. (2017) Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease. Graefes Arch Clin Exp Ophthalmol 255:1307-1317
Hariri, Amir H; Zhang, Hong Yang; Ho, Alexander et al. (2016) Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography. JAMA Ophthalmol 134:628-35
Ramachandran, Rithambara; X Cai, Cindy; Lee, Dongwon et al. (2016) Reliability of a Manual Procedure for Marking the EZ Endpoint Location in Patients with Retinitis Pigmentosa. Transl Vis Sci Technol 5:6
Sadda, SriniVas R; Chakravarthy, Usha; Birch, David G et al. (2016) CLINICAL ENDPOINTS FOR THE STUDY OF GEOGRAPHIC ATROPHY SECONDARY TO AGE-RELATED MACULAR DEGENERATION. Retina 36:1806-22

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