The overall goal of proposed research is to gain further knowledge of the physiology and pharmacology of aqueous outflow in the human eye.In proposed studies, the investigators have chosen to look at two general classes of drugs used therapeutically in the treatment of glaucoma; adrenergic agents and cholinergic agents.
The specific aims are to characterize outflow facility responses to these drugs in her recently described human isolated outflow pathway perfusion model, to map the distribution of drug receptors in outflow tissues, and to characterize relevant second messenger systems. This three-pronged approach, coordinating studies in physiology, biochemistry, and molecular biology, has the potential for producing a wealth of information greater than the sum of each individual approach in isolation. Recent refinements in molecular biology techniques and their applications is revolutionizing the diagnosis and treatment of disease, as well as basic medical research. The investigator's hope that her approach, using this powerful new technology in conjunction with the human TM model will allow her to develop a composite map of the human outflow system which will localize groups of cells which mediate changes in outflow resistance and characterize the second messenger systems which are coupled to these changes. Enhanced understanding of the basic mechanism(s) underlying normal outflow physiology may lend new insight into the pathogenesis of primary open angle glaucoma, and probably will facilitate the development of more effective, specific, and safe antiglaucoma drugs.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY007321-05
Application #
3264191
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1989-04-01
Project End
1996-03-31
Budget Start
1993-04-01
Budget End
1994-03-31
Support Year
5
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Massachusetts Eye and Ear Infirmary
Department
Type
DUNS #
073825945
City
Boston
State
MA
Country
United States
Zip Code
02114
Zhang, X; Wang, N; Schroeder, A et al. (2000) Expression of adenylate cyclase subtypes II and IV in the human outflow pathway. Invest Ophthalmol Vis Sci 41:998-1005
Erickson, K A; Schroeder, A (2000) Direct effects of muscarinic agents on the outflow pathways in human eyes. Invest Ophthalmol Vis Sci 41:1743-8
Siegner, S W; Netland, P A; Schroeder, A et al. (2000) Effect of calcium channel blockers alone and in combination with antiglaucoma medications on intraocular pressure in the primate eye. J Glaucoma 9:334-9
Zhang, X; Schroeder, A; Erickson, K A (1999) Effect of continuous administration of a cholinergic agonist on [3H]4-DAMP binding and m3 mRNA expression in cultured human ciliary muscle cells. J Ocul Pharmacol Ther 15:153-63
Al-Aswad, L A; Gong, H; Lee, D et al. (1999) Effects of Na-K-2Cl cotransport regulators on outflow facility in calf and human eyes in vitro. Invest Ophthalmol Vis Sci 40:1695-701
Zhang, X; Hernandez, M R; Yang, H et al. (1995) Expression of muscarinic receptor subtype mRNA in the human ciliary muscle. Invest Ophthalmol Vis Sci 36:1645-57
Erickson, K A; Schroeder, A; Netland, P A (1995) Verapamil increases outflow facility in the human eye. Exp Eye Res 61:565-7
Schuman, J S; Erickson, K; Nathanson, J A (1994) Nitrovasodilator effects on intraocular pressure and outflow facility in monkeys. Exp Eye Res 58:99-105
Erickson, K; Liang, L; Shum, P et al. (1994) Adrenergic regulation of aqueous outflow. J Ocul Pharmacol 10:241-52
Liang, L L; Epstein, D L; de Kater, A W et al. (1992) Ethacrynic acid increases facility of outflow in the human eye in vitro. Arch Ophthalmol 110:106-9

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