Our goal is to develop and evaluate several clinical electrophysiological tests which may enhance our ability to diagnose and manage disease. We are concerned primarily with two areas, tests of retinal pigment epithelial (RPE) function, and tests of dopaminergic retinal pathways that may correlate with disorders such as schizophrenia. The assessment of RPE function is important because the RPE is involved in a wide variety of ocular disorders. No specific diagnostic tests for the RPE currently exist, and we will investigate several potential candidates: 1) the fast oscillation, a light-induced response generated at the basal RPE membrane; 2) a standing potential response, produced without light by making the subject hypoxic and then restoring oxygenation suddenly; 3) changes in the standing potential induced by intravenous injection of a hyperosmolar solution or acetazolamide. All of these responses can be recorded for clinical purposes with the EOG. We will first work with normal subjects to standardize the tests and develop protocols that are suitable for general clinical use. We will then study patients with known retinal and RPE disease to evaluate diagnostic specificity, and, if warranted, extend the evaluation to a larger group of patients undergoing prospective electrophysiologic testing. We will also complete some studies on the c-wave, although our previous work has shown this response encounters difficulties as a clinical procedure. Objective criteria for diagnosing or following schizophrenia are critically needed. Dopaminergic neural processes have been implicated in disorders such as schizophrenia or Parkinson's disease, and also may contribute to the oscillatory potentials of the ERG. We will investigate whether oscillatory potential changes can be associated with schizophrenia or with Parkinson's disease.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005831-03
Application #
3261464
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1985-09-30
Project End
1988-09-29
Budget Start
1987-09-30
Budget End
1988-09-29
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Mori, T; Pepperberg, D R; Marmor, M F (1990) Dark adaptation in locally detached retina. Invest Ophthalmol Vis Sci 31:1259-63
Marmor, M F; Yao, X Y (1989) The enhancement of retinal adhesiveness by ouabain appears to involve cellular edema. Invest Ophthalmol Vis Sci 30:1511-4
Yoon, Y H; Marmor, M F (1989) Dextromethorphan protects retina against ischemic injury in vivo. Arch Ophthalmol 107:409-11
Kawano, S; Mori, T; Marmor, M F (1988) The effect of choroidal congestion in retinal pigment epithelium function and the electroretinogram. Doc Ophthalmol 69:221-5
Marmor, M F; Hock, P; Schechter, G et al. (1988) Oscillatory potentials as a marker for dopaminergic disease. Doc Ophthalmol 69:255-61
Mori, T; Tsue, T T; Marmor, M F (1988) Electrical responses from detached retina inside the intact rabbit eye. Invest Ophthalmol Vis Sci 29:1040-3
Yoon, Y H; Marmor, M F (1988) Rapid enhancement of retinal adhesion by laser photocoagulation. Ophthalmology 95:1385-8