Parallel human and primate studies of the pathophysiologic mechanisms of ocular hypotony in eyes with ciliochoroidal detachment, cyclodialysis, iridocyclitis, and retinal detachment will be undertaken. Primate models of each of these disorders have been developed. Previous studies have indicated a key role for uveoscleral outflow in the pathogenesis of hypotony. Therefore, characterization of the physiology and anatomy of the uveoscleral outflow pathway will be performed. The intraocular pressure dependence, suprachoroidal hydrostatic pressure, and permeability of the ciliary musle interstitial spaces will be evaluated with fluorophotometry and flurorescence microccopy in normal eyes. The extravascular protein concentration and vascular permeability of the uvea will also be determined. In monkey eyes with ciliochoroidal detachment of iridocyclitis, the uveoscleral outflow rate and extravascular protein concentration and ciliary muscle permeability will be measured. The underlying hypothesis to be studied in the pathogenesis of hypotony is increased fluid permeability of the ciliary muscle interstitial spaces due to an increase in extravascular protein concentration due to abnormal vascular permeability. In a model of chronic rhegmatogenous retinal detachment, previous studies have strongly argued for the presence of posterior fluid movement through the virtreous, into the subretinal space, and across the RPE. From vitreous fluorophotometry, measurement of the inward and outward permeability of the blood retinal barrier (RPE) of carboxyfluorescein allows calculation of five physiologic parameters: (1) diffusional permeability of RPE to carboxyfluorescein, (2) rate of solute-linked water transport, (3) osmotic fluid permeability of the RPE, (4) hydrostatic fluid permeability of the RPE, and (5) active carboxyfluorescein transport of the RPE. These parameters will be measured in monkeys with normal eyes, eyes with acute, sub-acute, or chronic retinal detachment, following cryopexy, and after retinal detachment repair. The effects of various drugs will also be studied. Patients with hypotony from ciliochoroidal detachment, cyclodialysis or chronic iridocyclitis will be studied with aqueous fluorophotometry to measure the aqueos flow rate. The episcleral venous pressure will also be measured. In summary, the pathophysiologic mechanisms of ocular hypotony will be studied with special emphasis on unconventional aqueous outflow pathways.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY003277-09
Application #
3257584
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1979-07-01
Project End
1992-06-30
Budget Start
1987-07-01
Budget End
1988-06-30
Support Year
9
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Toris, C B; Pederson, J E; Tsuboi, S et al. (1990) Extravascular albumin concentration of the uvea. Invest Ophthalmol Vis Sci 31:43-53
Emi, K; Pederson, J E; Toris, C B (1989) Hydrostatic pressure of the suprachoroidal space. Invest Ophthalmol Vis Sci 30:233-8
Tsuboi, S; Pederson, J E (1988) Volume flow across the isolated retinal pigment epithelium of cynomolgus monkey eyes. Invest Ophthalmol Vis Sci 29:1652-5
Tsuboi, S; Pederson, J E (1988) Effect of plasma osmolality and intraocular pressure on fluid movement across the blood-retinal barrier. Invest Ophthalmol Vis Sci 29:1747-9
Tsuboi, S; Pederson, J E (1987) Acetazolamide effect on the inward permeability of the blood-retinal barrier to carboxyfluorescein. Invest Ophthalmol Vis Sci 28:92-5
Tsuboi, S; Pederson, J E (1987) Permeability of the blood-retinal barrier to carboxyfluorescein in eyes with rhegmatogenous retinal detachment. Invest Ophthalmol Vis Sci 28:96-100
Toris, C B; Pederson, J E (1987) Aqueous humor dynamics in experimental iridocyclitis. Invest Ophthalmol Vis Sci 28:477-81
Toris, C B; Gregerson, D S; Pederson, J E (1987) Uveoscleral outflow using different-sized fluorescent tracers in normal and inflamed eyes. Exp Eye Res 45:525-32
Pederson, J E; Toris, C B (1987) Uveoscleral outflow: diffusion or flow? Invest Ophthalmol Vis Sci 28:1022-4
Tsuboi, S; Pederson, J E; Toris, C B (1987) Functional recovery of retinal pigment epithelial damage in experimental retinal detachment. Invest Ophthalmol Vis Sci 28:1788-94

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