Effects of pegaptanib sodium on retinal function in isolated perfused vertebrate retina

Matthias Lüke*, Kai Januschowski, Aysegül Tura, Julia Lüke, Khaled Nassar, Christoph Lüke, Toni Schneider, Peter Szurman, Salvatore Grisanti, Karl Ulrich Bartz-Schmidt

*Corresponding author for this work
6 Citations (Scopus)

Abstract

Purpose: To evaluate the short-term toxic effects of pegaptanib sodium on retinal function. At present, intraocular anti-vascular endothelial growth factor (VEGF) therapy is the primary choice of treatment for neovascular maculopathy. The isoform VEGF165 is specifically inhibited by pegaptanib sodium. Therefore, since VEGF165 has neuroprotective effects against apoptosis of neuronal cells, blockage of VEGF165 by pegaptanib could induce retinal dysfunction. In the present study, we used an electrophysiological technique for testing retinal toxicity in order to evaluate the short-term toxic effects of pegaptanib sodium on retinal function in a model of isolated perfused vertebrate retina. Methods: Isolated bovine retinas were perfused with an oxygenated, pre-incubated nutrient solution. Electroretinograms (ERGs) were recorded as trans-retinal potentials using Ag/AgCl electrodes. Pegaptanib sodium (0.006, 0.06, or 0.2mg/ml) and solvent carrier were added to the nutrient solution for 45min. ERGs were monitored before, during, and after exposure. Results: No significant reductions of b-wave (p=0.357, p=0.31, and p=0.11, respectively) or a-wave (p=0.189, p=0.46, and p=0.23, respectively) amplitudes were detected during application of pegaptanib (0.006, 0.06, or 0.2mg/ml). The solvent carrier alone had no effect on ERG b- or a-waves (p=0.98 and p=0.42, respectively). During washout, ERG amplitudes of all test series remained unchanged. Conclusion: Results suggest that both pegaptanib sodium and its solvent carrier have good safety profiles. Intraocular application of 0.3mg pegaptanib sodium induced no significant changes in ERGs in our ex vivo model and, thus, appears to be safe.

Original languageEnglish
JournalCurrent Eye Research
Volume35
Issue number3
Pages (from-to)248-254
Number of pages7
ISSN0271-3683
DOIs
Publication statusPublished - 03.2010

Research Areas and Centers

  • Research Area: Luebeck Integrated Oncology Network (LION)

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