J Korean Ophthalmol Soc.  2015 Apr;56(4):586-591. 10.3341/jkos.2015.56.4.586.

Effect of Bimatoprost on the Permeability of Trabecular Meshwork Cell Monolayer

Affiliations
  • 1Department of Ophthalmology, Catholic University of Daegu School of Medicine, Daegu, Korea. jwkim@cu.ac.kr

Abstract

PURPOSE
To investigate the effects of bimatoprost on the permeability of cultured human trabecular meshwork cells (HTMC) monolayer.
METHODS
HTMCs were cultured until confluency in the inner Transwell chamber and then exposed to benzalkonium chloride, brimonidine, latanoprost or bimatoprost for 1 week. Carboxyfluorescein permeability through the HTMC monolayer was measured using a spectrofluorometer after 2 hours in the outer chamber. Cellular viability was assessed using the MTT assay.
RESULTS
Each drug diluted at 1/1000X did not affect the cellular survival (p > 0.05). Brimonidine, latanoprost and bimatoprost did not affect the carboxyfluorescein permeability through the HTMC monolayer (p > 0.05). The carboxyfluorescein permeability was not different between latanoptost and bimatoprost after 1 week of exposure (p > 0.05).
CONCLUSIONS
Bimatoprost, a drug known to increase trabecular outflow, does not affect the carboxyfluorescein permeability through the HTMC monolayer. Thus, the effect on the trabecular outflow of bimatoprost may not be significant.

Keyword

Bimatoprost; Carboxyfluorescein; Permeability; Trabecular meshwork cells

MeSH Terms

Benzalkonium Compounds
Humans
Permeability*
Trabecular Meshwork*
Bimatoprost
Brimonidine Tartrate
Benzalkonium Compounds

Figure

  • Figure 1. Photograph of confluently cultured trabecular meshwork cells in monolayer (×100).

  • Figure 2. Effects of BAC, BMD, LAT and BIM on the survival of trabecular meshwork cells. Each drug did not decrease cellular viability significantly ( p > 0.05). BAC = benzalkonium chloride; BMD = brimonidine; LAT = latanoprost; BIM = bimatoprost.

  • Figure 3. Effects of BAC, BMD, and BIM on the permeability of carboxyfluorescin through the trabecular meshwork cell monolayer. Each drug did not affect on the permeabilty of carboxyfluorescein significantly compared control using PBS ( p > 0.05). Carboxyfluorescein intensity of outer chamber normalized to the mean value obtained using PBS (permeability 100%). PBS = phosphate buffered saline; BAC = benzalkonium chloride; BMD = brimonidine; BIM = bimatoprost.

  • Figure 4. Comparison of the permeability of carboxyfluorescin through the trabecular meshwork cell monolayer between LAT and BIM. There is no significant difference of the permeabilty of carboxyfluorescein between LAT and BIM ( p > 0.05). Carboxyfluorescein intensity of outer chamber normalized to the mean value obtained using PBS (permeability 100%). PBS = phosphate buffered saline; LAT = latanoprost; BIM = bimatoprost.


Reference

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