Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage

• Published in: Scientific reports 2014-10, Vol.4 (1), p.6501-6501, Article 6501
• Main Authors: Fujishiro, Takashi, Kawasaki, Hiroshi, Aihara, Makoto, Saeki, Tadashiro, Ymagishi, Reiko, Atarashi, Takuya, Mayama, Chihiro, Araie, Makoto
• Format: Article
• Language: English
• Subjects: 59; 692/308/1426; 692/308/1892; Animal models; Animals; Anterior chamber; Binocular vision; Cell death; Central Nervous System; Cholera toxin; Cholera toxin B subunit; Degeneration; Disease Models, Animal; Eye; Ferrets; Geniculate Bodies - physiopathology; Glaucoma; Glaucoma - physiopathology; Humanities and Social Sciences; Humans; Hypertension; Injection; Lateral geniculate nucleus; multidisciplinary; Ocular Hypertension - physiopathology; Optic nerve; Optic neuropathy; Retina; Retinal ganglion cells; Retinal Ganglion Cells - pathology; Science; Toxins; Vision, Binocular - physiology; Visual Pathways - physiopathology; Wallerian Degeneration - physiopathology; Waterborne diseases
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep06501

Glaucoma optic neuropathy (GON) is a condition where pathogenic intraocular pressure (IOP) results in axonal damage following retinal ganglion cell (RGC) death and further results in secondary damage of the lateral geniculate nucleus (LGN). Therapeutic targets for glaucoma thus focus on both the LGN and RGC. However, the temporal and spatial patterns of degeneration and the mechanism of LGN damage have not been fully elucidated. Suitable and convenient ocular hypertension (OH) animal models with binocular vision comparable to that of monkeys are strongly needed. The ferret is relatively small mammal with binocular vision like humans – here we report on its suitability for investigating LGN. We developed a new method to elevate IOP by injection of cultured conjunctival cells into the anterior chamber to obstruct aqueous outflow. Histologically, cultured conjunctival cells successfully proliferated to occlude the angle and IOP was elevated for 13 weeks after injection. Macroscopically, the size of the eye gradually expanded. Subsequent enlargement of optic nerve head cupping and atrophic damage of LGN projected from the OH eye were clearly observed by anterograde staining with cholera toxin B. We believe the ferret may be a promising OH model to investigate secondary degeneration of central nervous system including LGN.