PT  - JOURNAL ARTICLE
AU  - M Lüke
AU  - M Warga
AU  - F Ziemssen
AU  - F Gelisken
AU  - S Grisanti
AU  - T Schneider
AU  - C Lüke
AU  - M Partsch
AU  - K U Bartz-Schmidt
AU  - P Szurman
TI  - Effects of bevacizumab on retinal function in isolated vertebrate retina
AID  - 10.1136/bjo.2006.094995
DP  - 2006 Sep 01
TA  - British Journal of Ophthalmology
PG  - 1178--1182
VI  - 90
IP  - 9
4099  - http://bjo.bmj.com/content/90/9/1178.short
4100  - http://bjo.bmj.com/content/90/9/1178.full
SO  - Br J Ophthalmol2006 Sep 01; 90
AB  - Background: Bevacizumab (Avastin) is a recombinant protein that targets vascular endothelial growth factor (VEGF). In vitro, bevacizumab inhibits VEGF induced cell proliferation and tissue factor production. Abnormal angiogenesis involving VEGF is a central event during the development of choroidal neovascularisation (CNV). The present study was designed to evaluate the short term toxic effects of bevacizumab on retinal function for a therapeutic intraocular application. Methods: Isolated bovine retinas were perfused with an oxygen pre-incubated nutrient solution. The electroretinogram (ERG) was recorded as a transretinal potential using silver/silver chloride electrodes. Bevacizumab was added in different concentrations to the nutrient solution for 45 minutes. Thereafter the retina was reperfused for 60 minutes with normal nutrient solution. The percentage of a-wave and b-wave reduction during the application of bevacizumab was calculated and compared to control recordings. Results: During the application of three different concentrations of bevacizumab (0.08 mg/ml, 0.25 mg/ml, 0.8 mg/ml) no significant reduction of the a-wave and b-wave amplitude was observed. During the washout, the ERG amplitudes were unchanged. Conclusion: The present study suggests that an intraocular application of 0.25 mg/ml bevacizumab for the treatment of CNV is reasonable. No significant short term effects of bevacizumab on retinal function were detected, but long term effects cannot be excluded.