We have confirmed the usefulness of the rat model of chronic, moderately el
evated intraocular pressure (IOP) for studying loss of retinal ganglion cel
ls, and as a model for pharmacological neuroprotection studies that may be
relevant to treating human glaucoma. By unilaterally cauterizing three epis
cleral vessels, as described previously in the literature by another labora
tory, we observed an approximately 1.6-fold increase in IOP compared to the
contralateral eye (18.6 vs 11.5 mm Hg, respectively), Elevated IOP persist
ed for 6 months without re-treatment. Cupping of the optic disk was observa
ble by examination, in vivo. In 6 months, there was an approximately 40 % l
oss of retinal ganglion cells in the peripheral retina. This model provides
a reproducible and quantitative model for pharmacological experiments usin
g neuroprotective agents. (C) 1999 Academic Press.