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Purpose: Subretinal prostheses are a novel technology for restoring useful vision in patients with retinitis pigmentosa or age-related macular degeneration. We characterize the surgical implantation technique and functional time window of an acute rabbit eye model for testing of human subretinal prostheses.
Methods: Retinal prostheses were implanted subretinally in 26 rabbits using a two-step technique. Fundus imaging, fluorescein fundus angiography, and optical coherence topography (OCT) were conducted postoperatively from days 1 to 21 to monitor prosthesis positioning and retinal anatomic changes.
Results: Successful implantation and excellent retina apposition were achieved in 84.6% of the rabbits. OCTs showed the overlying retina at full thickness for the first 2 days after implantation. Histology confirmed intact inner layers of the overlying retina until day 3. Progressive atrophy of the overlying retina was revealed by repeated OCTs; approximately 40% of the retina thickness remained on postoperative days 5 and 6.
Conclusions: The two-step implantation technique works well for the rabbit eye model with human prostheses. Rabbit retina may be used for acute electrophysiologic testing of a retinal prosthesis, but is unsuitable for chronic studies due to the merangiotic retina and its limited time window of validity.
Translational Relevance: The improved efficacy in prosthesis surgery using this technique will circumvent the challenges in animal models that provide human-like features critical for the transition into human clinical trials.
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http://dx.doi.org/10.1167/tvst.8.5.20 | DOI Listing |
Invest Ophthalmol Vis Sci
September 2025
Truhlsen Eye Institute, University of Nebraska Medical Center, Omaha, Nebraska, United States.
Purpose: This study reports the changes in aqueous humor dynamics (AHD) and biometric parameters associated with growth and maturation in male Dutch-belted rabbits.
Methods: In this prospective observational study, 20 male Dutch-belted rabbits were studied at 4-weekly intervals starting at 10 weeks through 38 weeks of age. Data collected included intraocular pressure (IOP), aqueous flow, outflow facility by tonography and fluorophotometry (acetazolamide method), episcleral venomanometry, central corneal thickness, corneal diameter, anterior chamber depth, and testicular volume.
Drug Metab Dispos
August 2025
Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc, South San Francisco, California. Electronic address:
Hydrolases in the eye play an important role in the metabolism of ophthalmic drugs, especially those administered locally to the eyes. With the growing interest in peptide-based therapeutics for treating eye disease, it has become increasingly important to characterize the enzymatic activities of ocular tissues against both small molecules and peptides to better understand their ocular metabolism. In this study, we characterized the activities of hydrolases, including carboxylesterase 1 and 2, arylacetamide deacetylase, paraoxonases, cytidine deaminase, fatty-acid amide hydrolase, and peptidases by incubating probe substrates in whole eye homogenates and vitreous humors from human donors and 3 preclinical species, including New Zealand White rabbits, Gottingen minipigs, and Cynomolgus monkeys.
View Article and Find Full Text PDFOphthalmol Sci
July 2025
Vanderbilt University Medical Center, Nashville, Tennessee.
Purpose: To assess whether levels of topotecan that are expected to be therapeutic against retinoblastoma tumors can be achieved within the retina and choroid by suprachoroidal injection (SCI) and to assess toxicity and safety in vivo.
Design: Pharmacokinetics and dose escalation toxicity study.
Subjects: New Zealand white rabbits.
Transl Vis Sci Technol
September 2025
Ineye Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Purpose: To evaluate Periplaneta americana extract (PAE) effects on corneal epithelial healing and fibrosis after superficial lamellar keratectomy (SLK) in rabbits.
Methods: SLK was performed on the right eyes of 48 New Zealand White rabbits, randomized into three treatment groups (n = 16/group): normal saline (NS), Tobradex eye drops (TE), and PAE group. Corneal opacity and epithelial defect area were quantified using slit-lamp imaging at postoperative days 3, 7, 14, and 28 (D3, D7, D14, and D28) and scored via the grading system.
Exp Eye Res
September 2025
Department of Cell Biology and Histology, School of Medicine and Nursing, University of the Basque Country UPV/EHU, 48940, Leioa, Spain; BEGIKER Ophthalmology Research Group, Biobizkaia Health Research Institute, 48903, Barakaldo, Spain. Electronic address:
The objective of this study was to develop a reliable, cost-effective, and rapid in vitro model employing real-time PCR to assess inflammatory responses in hydrogel-based systems, and to comparatively evaluate the anti-inflammatory efficacy of human serum (HS), serum derived from plasma rich in growth factors (sPRGF), and human amniotic membrane extracts (HAMe) incorporated into gelatin-based hydrogels. An in vitro model of corneal inflammation was established by quantifying IL-1β expression via qPCR in TNFα-stimulated SV-40 immortalised human corneal epithelial (HCE) cells. Hydrogels functionalised with HS, sPRGF, or HAMe sourced from proximal, medial, distal, or pooled amniotic regions were evaluated for their anti-inflammatory potential.
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