Safe dose of intravitreal imatinib and its effect on laser-induced choroidal neovascularization: A rat-model experiment

被引:4
|
作者
Nikkhah H. [1 ,6 ]
Ahmadieh H. [2 ]
Ramezani A. [3 ]
Rezaei Kanavi M. [1 ]
Hosseini S.B. [1 ]
Sadeghi N. [4 ]
Khandaghy Meybodi S.M. [2 ]
Yaseri M. [5 ]
机构
[1] Shahid Beheshti University of Medical Sciences, Ocular Tissue Engineering Research Center, Tehran
[2] Shahid Beheshti University of Medical Sciences, Ophthalmic Research Center, Tehran
[3] Shahid Beheshti University of Medical Sciences, Ophthalmic Epidemiology Research Center, Tehran
[4] Tehran University of Medical Sciences, Department of Drug and Food Control, School of Pharmacy, Tehran
[5] Tehran University of Medical Sciences, Department of Biostatistics and Epidemiology, Tehran
[6] Ophthalmic Research Center, No. 23, Boostan 9 St., Pasdaran Ave, Tehran
关键词
Choroidal neovascularization; Fluorescein angiography; Imatinib; Platelet derived growth factor; Rat;
D O I
10.1186/s40942-015-0017-4
中图分类号
学科分类号
摘要
Background: This two-phase experimental study was conducted to determine the maximum safe dose of intravitreal imatinib (IVI) and its inhibitory effect on a rat model of choroidal neovascularization (CNV). Methods: In phase I, 60 rats were divided into six groups (A to F); five of which received IVI with concentrations of 330 (A), 250 (B), 165 (C), 80 (D), and 40 (E) μg/5 μl, and the control group (F) received balanced salt solution (BSS). In addition to electroretinography (ERG), routine histopathological analysis and immunohistochemistry for glial fibrillary acidic protein were performed. In phase II, CNV was induced by laser photocoagulation in 25 rats and the animals were divided into two groups. One group received the maximum safe dose of IVI, determined in phase I, and the other received intravitreal BSS. After 4 weeks, the groups were compared in terms of mean scores of fluorescein leakage in fluorescein angiography and the mean CNV areas in histopathological sections. Results: In phase I, ERG and the histopathological findings revealed retinal toxicity in groups A to D and A to C, respectively; therefore, a dose of 40 μg/5 μl imatinib was specified as the maximum safe dose for phase II. In phase II, late phase fluorescein leakage and the CNV areas were not significantly different between the imatinib-treated eyes and the controls (p = 0.62 and p = 0.5, respectively). Conclusions: Despite the safety of IVI with a dose of 40 μg/5 μl, no inhibitory effect on laser-induced CNV was observed. Further studies are required to investigate the possible synergistic effects of Imatinib with conventional anti-CNV drugs. © 2015 Nikkhah et al.
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