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Oxygen-Induced Retinopathy Model for Ischemic Retinal Diseases in Rodents
Published on: September 16, 2020
The HIF-1 antagonist acriflavine: visualization in retina and suppression of ocular neovascularization
Mingbing Zeng1,2,3, Jikui Shen1,2, Yuanyuan Liu1,2
1Institute for Cell Engineering, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Abstract:
Acriflavine, a fluorescent drug previously used for bacterial and trypanosomal infections, reduces hypoxia-inducible factor-1 (HIF-1) and HIF-2 transcriptional activity. In mice with oxygen-induced ischemic retinopathy, intraocular or intraperitoneal injections of acriflavine caused dose-dependent suppression of retinal neovascularization (NV) and significantly reduced expression of HIF-1-responsive genes. Intraocular injection of 100 ng caused inner retina fluorescence within 1 h that was seen throughout the entire retina between 1 and 5 days, and at 7 days after injection, strongly suppressed choroidal NV at Bruch's membrane rupture sites. After suprachoroidal injection of 300 ng in rats, there was retinal fluorescence in the quadrant of the injection at 1 h that spread throughout the entire retina and choroid by 1 day, was detectable for 5 days, and dramatically reduced choroidal NV 14 days after rupture of Bruch's membrane. After topical administration of acriflavine in mice, fluorescence was seen in the retina and retinal pigmented epithelium within 5 min and was detectable for 6-12 h. Administration of 0.5% drops to the cornea twice a day significantly reduced choroidal NV in mice. Electroretinographic b-wave amplitudes were normal 7 days after intravitreous injection of 100 ng of acriflavine in mice, showed mild threshold reductions at highest stimulus intensities after injection of 250 ng, and more extensive changes after injection of 500 ng. These data provide additional evidence for an important role for HIF-1 in retinal and choroidal NV and suggest that acriflavine can target HIF-1 through a variety of modes of administration and has good potential to provide a novel therapy for retinal and choroidal vascular diseases.
Key Message:
Acriflavine, an inhibitor of HIF-1, suppresses retinal and choroidal neovascularization. HIF-1 plays a critical role in ocular neovascularization. Acriflavine's fluorescence provides a mean to track its entry and exit from the retina. Acriflavine has therapeutic potential for the treatment of ocular neovascularization.
Insights
Acriflavine, a drug targeting hypoxia-inducible factor-1 (HIF-1), effectively suppresses abnormal blood vessel growth in the eye. This study shows acriflavine
Area of Science:
- Ophthalmology
- Pharmacology
- Molecular Biology
Background:
- Hypoxia-inducible factor-1 (HIF-1) is a key regulator of cellular responses to low oxygen.
- Ocular neovascularization (NV) is a major cause of vision loss, often driven by HIF-1.
- Acriflavine is a fluorescent drug with known antimicrobial properties.
Purpose of the Study:
- To investigate the potential of acriflavine as a therapeutic agent for ocular neovascularization.
- To evaluate the effect of acriflavine on HIF-1 and HIF-2 transcriptional activity.
- To assess the efficacy of acriflavine in preclinical models of retinal and choroidal neovascularization.
Main Methods:
- Administration of acriflavine via intraocular, intraperitoneal, and topical routes in mouse and rat models.
- Assessment of acriflavine's fluorescence and distribution within the retina and choroid.
- Quantification of retinal and choroidal neovascularization.
- Measurement of HIF-1-responsive gene expression.
- Evaluation of retinal function using electroretinography.
Main Results:
- Acriflavine significantly reduced retinal and choroidal neovascularization in a dose-dependent manner.
- Fluorescence imaging confirmed acriflavine's penetration into the retina and choroid.
- Topical administration of acriflavine demonstrated efficacy in reducing choroidal neovascularization.
- Electroretinography showed minimal impact on retinal function at therapeutic doses.
Conclusions:
- Acriflavine effectively inhibits HIF-1 activity, thereby suppressing ocular neovascularization.
- The drug can be administered through various routes, including topical application.
- Acriflavine shows promise as a novel therapeutic for retinal and choroidal vascular diseases.
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