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PURPOSE: To establish an experimental model of ocular hypertension in the mouse. METHODS: Twenty-two black Swiss mice were used. After anesthesia and pupil dilation, the anterior chamber was flattened by the aspiration of aqueous humor. Laser photocoagulation (532-nm wavelength, 200-mW power, 0.05-second duration, 200-μm spot size) then was performed at the limbus. Intraocular pressure (IOP) was measured weekly for four weeks and biweekly for 12 weeks, by a micro-needle method. Slit lamp biomicroscopy was performed throughout the period and the structural changes were assessed histologically. A treatment response was considered to be a success if either the mean of IOP measurements collected during the first four weeks was increased by 30% or more, or the mean of all measurements collected during the 12-week study period was increased by 30% or more. RESULTS: Laser-treated eyes showed significantly higher IOP than control eyes from one to six weeks (p < 0.001). The average IOP in treated eyes during the first four and 12 weeks was significantly higher than the control IOP (p < 0.001). These IOP increases were 7.1 and 3.8 mmHg, respectively. During the first four weeks, sustained elevation of IOP was obtained in 64% (14/22) of the treated eyes. During the entire 12-week study, increased IOP was successfully maintained in 37% (7/19) of the treated eyes. After six weeks, elevated IOP often returned to normal or several mmHg below normal. Histological analysis at the end of the 12-week study showed no inflammatory cells in the anterior segment and confirmed that the angle was closed by the laser photocoagulation treatment. CONCLUSIONS: This method produces persistent IOP elevation in mouse eyes and may be a promising experimental model for the investigation of the biological mechanisms of glaucomatous optic neuropathy.
Dr. M. Aihara, Hamilton Glaucoma Center, University of California San Diego, La Jolla, CA 92093, USA.
5 Experimental glaucoma; animal models