Ion pumps, cotransport systems and channels are present in animal cell membranes to maintain cellular ionic composition, to transport electrolytes and fluid across epithelia, and to regulate cell volume and maintain osmotic balance. Furthermore, in cornea and lens, epithelial ionic/fluid transport systems are critical for maintaining the transparency of these tissues. Although the functional integrity of the endothelium is essential for corneal transparency, the epithelium may also play a role. Because medical management of physiological function is limited, basic research that may lead to the development of methods to either enhance or limit fluid transport is highly relevant. Likewise, cataract is a prevalent health problem for which there is no medical treatment. Many mechanisms contribute to the maintenance of lens transparency. It is clear that among many unknown factors, osmotic equilibrium, Na/K ATPase activity and normal GSH levels are necessary for lens clarity. The overall aim of this proposal is to further characterize regulatory mechanisms of ion/fluid transport, membrane permeability, and related physiological parameters relevant to the understanding of corneal and lens cell function. In addition, some experiments will use the ciliary body epithelium, a tissue studied in this laboratory in the past: Electrophysiological, radiolabeled tracer and fluorometric techniques will be used in three specific aims: l) Characterization of water permeability (P-f and P-dw) and its regulation in corneal, lens and ciliary body epithelia; 2) Characterization of the distribution of ionic currents and conductances around the lens surface; and 3) Characterization of Na-K-2Cl cotransport activity in the lens.
These aims will extend recent original findings of this laboratory. From the accomplishment of these aims, models of lens and corneal physiological function will be provided.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY000160-26
Application #
2752310
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1976-12-01
Project End
2003-12-31
Budget Start
1999-01-01
Budget End
1999-12-31
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
114400633
City
New York
State
NY
Country
United States
Zip Code
10029
Candia, Oscar A; Gerometta, Rosana M; Danias, John (2014) Tissue plasminogen activator reduces the elevated intraocular pressure induced by prednisolone in sheep. Exp Eye Res 128:114-6
Alvarez, Lawrence J; Zamudio, Aldo C; Candia, Oscar A (2013) Sildenafil stimulates aqueous humor turnover in rabbits. Exp Eye Res 111:67-70
Gerometta, Rosana; Kumar, Sandeep; Shah, Shaily et al. (2013) Reduction of steroid-induced intraocular pressure elevation in sheep by tissue plasminogen activator. Invest Ophthalmol Vis Sci 54:7903-9
Wallace, Julian M; Chiu, Michael K; Nandy, Anirvan S et al. (2013) Crowding during restricted and free viewing. Vision Res 84:50-9
Gerometta, Rosana; Alvarez, Lawrence J; Candia, Oscar A (2012) Sildenafil accelerates anterior chamber refilling after paracentesis in sheep and rabbits. Invest Ophthalmol Vis Sci 53:565-73
Candia, Oscar A (2011) Surface and volume changes in the lens during accommodation. Invest Ophthalmol Vis Sci 52:3698
Gerometta, Rosana; Escobar, D; Candia, Oscar A (2011) An hypothesis on pressure transmission from anterior chamber to optic nerve. Med Hypotheses 77:827-31
Gerometta, Rosana; Alvarez, Lawrence J; Candia, Oscar A (2011) Effect of sildenafil citrate on intraocular pressure and blood pressure in human volunteers. Exp Eye Res 93:103-7
Zamudio, Aldo C; Candia, Oscar A (2011) Interaction between mechanical and osmotic forces in the isolated rabbit lens. Exp Eye Res 93:798-803
Candia, O A; Zamudio, A C; Alvarez, L J (2010) Mechanical stretching forces oppose osmotic lens swelling. Exp Eye Res 91:472-4

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