Objective : To create an experimental glaucoma model which is simple and highly reproducible and stable in the albino rabbit.
Materials and methods : We injected approximately 0.1ml, 0.2ml, 0.25ml, or 0.3ml of 3% atelocollagen into the anterior chamber of one eye of adult albino rabbits with a 30-gauge needle after aqueous humor paracentesis (approximately 0.2ml). After 1, 7, 14, 28, and 56 days of intracameral injection, we measured the intraocular pressure (IOP) with a Tono-Pen XL tonometer, and examination of the anterior ocular segment was performed. Intracameral injection of atelocollagen was applied to one eye of rabbits with the fellow eye serving as a control. 56 days after intracameral injection, we sacrificed the rabbits and excised the eyes for histological analysis.
Results : In all of the 7 eyes, which were injected with 0.1ml (n = 4) or 0.2ml (n = 4) of 3 % atelocollagen, elevated IOP (>20mmHg) was not maintained until 7 days after treatment. In all 7 eyes, which were injected with 0.25ml of 3% atelocollagen, elevated IOP (>20mmHg) was maintained until 56 days after treatment. Elevated IOP (>20mmHg) was also maintained until 56 days after treatment in 3 of 4 eyes that were injected with 0.3ml of 3% atelocollagen. In the remaining eye, however, the IOP decreased to < 20mmHg with in 2 days after the injection. Corneal neovascularization was observed in all atelocollagen-injected eyes, whereas the anterior ocular segment was subinflammatory. Histological analysis demonstrated that degenerated and vacuolated cells were observed in the retinal ganglion cell layer of the ocular hypertensive eye. A few TUNEL-positive cells were also seen. Conclusions : Creating an experimental glaucoma model by intracameral injection of 0.25ml of 3% atelocollagen was easy. This experimental model promises to be of value in further studies of glaucomatous optic nerve damage.
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