The long-term GOAL of this research is to elucidate the molecular modulation of ion transport processes in the conjunctiva. This research is built upon our encouraging preliminary finding that the pigmented rabbit conjunctiva appears to be a moderately tight, fluid-secreting barrier capable of active Cl- transport that is subject to cAMP modulation. Given that the conjunctival epithelium can transdifferentiate into the corneal epithelium under proper conditions, the present proposal seeks to test the hypothesis that the same ion transport processes in the corneal epithelium also exist in the conjunctiva. There are 3 SPECIFIC AIMS in this 3-year proposal: (1) To determine the relative contribution of various ion transport processes to the short-circuit current (Isc) in the pigmented rabbit conjunctiva. The focus will be on Na+/K+ ATPase, Cl- channel, Na+-K+-2Cl- (Na+-Cl-) cotransport, K+ channel, Na+ channel, Na+-glucose cotransport, Na+-amino acid cotransport, and Na+/H+ antiport; (2) To determine the influence of active Cl- secretion and Na+ absorption in water and-paracellular drug transport across the conjunctiva; and (3) To begin elucidating the regulatory mechanisms of Cl transport mediated by Ca2+, PKC, and particularly cAMP. The principal METHODOLOGY includes the measurement of (a) Isc, transmural resistance, and potential difference using the voltage clamp and Ussing chamber assembly; (b) transconjunctival net flux, uptake, and efflux of Na+, K+ (Rb+), and Cl- using a suitable radionuclide in the presence of various inhibitors and activators of ion transport processes; (c) transconjunctival water transport using a macromolecular radiotracer dilution method; and (d) transconjunctival drug transport using mannitol and various FITC-dextrans as paracellular markers. The IMPORTANCE of this research is that it will set the stage for defining the role of ion transport in the regulation of conjunctival cell volume, mucin secretion, as well as electrolyte and fluid balance in the conjunctival microenvironment in health, aging, and various disease states. These diseases may include dry eye, hormonal deficiencies, autoimmune diseases, and inflammation. Further work will reveal how ion transport processes can be exploited through formulation design to maximize drug transport across the conjunctiva for targeting to the posterior segment tissues of the eye.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY010421-01A1
Application #
2164278
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1994-12-01
Project End
1997-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Southern California
Department
Other Health Professions
Type
Schools of Pharmacy
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Yang, Johnny J; Ann, David K; Kannan, Ram et al. (2007) Multidrug resistance protein 1 (MRP1) in rabbit conjunctival epithelial cells: its effect on drug efflux and its regulation by adenoviral infection. Pharm Res 24:1490-500
Hosoya, Ken-ichi; Lee, Vincent H L; Kim, Kwang-Jin (2005) Roles of the conjunctiva in ocular drug delivery: a review of conjunctival transport mechanisms and their regulation. Eur J Pharm Biopharm 60:227-40
Shiue, Michael H I; Gukasyan, Hovhannes J; Kim, Kwang-Jin et al. (2002) Characterization of cyclic AMP-regulated chloride conductance in the pigmented rabbit conjunctival epithelial cells. Can J Physiol Pharmacol 80:533-40
Shiue, M H; Kulkarni, A A; Gukasyan, H J et al. (2000) Pharmacological modulation of fluid secretion in the pigmented rabbit conjunctiva. Life Sci 66:PL105-11
Yang, J J; Kim, K J; Lee, V H (2000) Role of P-glycoprotein in restricting propranolol transport in cultured rabbit conjunctival epithelial cell layers. Pharm Res 17:533-8
Chang, J E; Basu, S K; Lee, V H (2000) Air-interface condition promotes the formation of tight corneal epithelial cell layers for drug transport studies. Pharm Res 17:670-6
Ueda, H; Horibe, Y; Kim, K J et al. (2000) Functional characterization of organic cation drug transport in the pigmented rabbit conjunctiva. Invest Ophthalmol Vis Sci 41:870-6
Yang, J J; Ueda, H; Kim, K et al. (2000) Meeting future challenges in topical ocular drug delivery: development of an air-interfaced primary culture of rabbit conjunctival epithelial cells on a permeable support for drug transport studies. J Control Release 65:11-Jan
Hosoya, K; Ueda, H; Kim, K J et al. (1999) Nucleotide stimulation of Cl(-) secretion in the pigmented rabbit conjunctiva. J Pharmacol Exp Ther 291:53-9
Hosoya, K I; Horibe, Y; Kim, K J et al. (1998) Carrier-mediated transport of NG-nitro-L-arginine, a nitric oxide synthase inhibitor, in the pigmented rabbit conjunctiva. J Pharmacol Exp Ther 285:223-7

Showing the most recent 10 out of 29 publications