TY - JOUR
T1 - Effects of pegaptanib sodium on retinal function in isolated perfused vertebrate retina
AU - Lüke, Matthias
AU - Januschowski, Kai
AU - Tura, Aysegül
AU - Lüke, Julia
AU - Nassar, Khaled
AU - Lüke, Christoph
AU - Schneider, Toni
AU - Szurman, Peter
AU - Grisanti, Salvatore
AU - Bartz-Schmidt, Karl Ulrich
N1 - Funding Information:
This research was supported by an independent grant from Pfizer Pharma GmbH, Berlin, Germany.
Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010/3
Y1 - 2010/3
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=77950853420&partnerID=8YFLogxK
U2 - 10.3109/02713680903503504
DO - 10.3109/02713680903503504
M3 - Journal articles
C2 - 20373885
AN - SCOPUS:77950853420
VL - 35
SP - 248
EP - 254
JO - Current Eye Research
JF - Current Eye Research
SN - 0271-3683
IS - 3
ER -