Tafluprost protects rat retinal ganglion cells from apoptosis in vitro and in vivo

Graefes Arch Clin Exp Ophthalmol. 2009 Oct;247(10):1353-60. doi: 10.1007/s00417-009-1122-6. Epub 2009 Jun 24.

Abstract

Background: To investigate whether tafluprost, which is a prostaglandin-related compound and an anti-glaucoma drug, has a direct anti-apoptotic effect in cultured retinal ganglion cells (RGCs) and rat RGCs in retinas with optic nerve crush (ONC).

Methods: RGC-5 cells were induced to undergo apoptosis by a serum deprivation and by exogenous glutamate. The level of cell death with or without tafluprost was monitored by an XTT assay and by immunocytochemistry with activated caspase-3. Changes in intracellular calcium ([Ca(2+)]i) levels were measured with fluo-4 fluorescence. Rat RGCs were degenerated by ONC. After topical instillation of tafluprost for 7 and 14 days, the numbers of retrograde-labeled RGCs were counted. Retinal flatmounts were subjected to terminal dUTP nick end labeling (TUNEL) staining to detect apoptotic cells.

Results: Tafluprost dose-dependently promoted RGC-5 cell viability with an optimum concentration of 3 microM (p = 0.006). Tafluprost significantly reduced caspase-3-positive cells and suppressed [Ca(+2)]i evoked by exogenous glutamate. The cGMP-dependent protein kinase inhibitor and KT-5823 partially blocked the rescue effect of tafluprost (p = 0.002). The survival rate of RGCs significantly increased in eyes treated with tafluprost (p = 0.01), and the prevalence of TUNEL-positive cells was significantly decreased 14 days after ONC (p < 0.001).

Conclusions: These data suggest that tafluprost has an anti-apoptotic effect in RGCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Calcium / metabolism
  • Calcium Channel Blockers / pharmacology
  • Carbazoles / pharmacology
  • Caspase 3 / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Culture Media, Serum-Free
  • Cyclic GMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic GMP-Dependent Protein Kinases / metabolism
  • Dose-Response Relationship, Drug
  • Glutamic Acid / pharmacology
  • In Vitro Techniques
  • Instillation, Drug
  • Intracellular Membranes / metabolism
  • Intraocular Pressure / drug effects
  • Male
  • Nerve Crush
  • Neuroprotective Agents / administration & dosage
  • Neuroprotective Agents / antagonists & inhibitors
  • Neuroprotective Agents / pharmacology*
  • Ophthalmic Solutions
  • Optic Nerve
  • Prostaglandins F / administration & dosage
  • Prostaglandins F / antagonists & inhibitors
  • Prostaglandins F / pharmacology*
  • Protein Kinase Inhibitors / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Retinal Ganglion Cells / drug effects
  • Retinal Ganglion Cells / enzymology
  • Retinal Ganglion Cells / physiology*
  • Time Factors

Substances

  • Calcium Channel Blockers
  • Carbazoles
  • Culture Media, Serum-Free
  • Neuroprotective Agents
  • Ophthalmic Solutions
  • Prostaglandins F
  • Protein Kinase Inhibitors
  • KT 5823
  • tafluprost
  • Glutamic Acid
  • Cyclic GMP-Dependent Protein Kinases
  • Caspase 3
  • Calcium