I. Sellesnavarro et al., RETINAL GANGLION-CELL DEATH AFTER DIFFERENT TRANSIENT PERIODS OF PRESSURE-INDUCED ISCHEMIA AND SURVIVAL INTERVALS - A QUANTITATIVE IN-VIVO STUDY, Investigative ophthalmology & visual science, 37(10), 1996, pp. 2002-2014
Purpose. To quantitate in vivo retinal ganglion cell (RGC) survival af
ter transient periods of pressure-induced ischemia of the rat retina a
nd after different survival intervals. Methods. In adult rats, RGCs we
re labeled with fluorogold applied to their main targets in the brain,
Seven days later, in several groups of rats, the left retinas were su
bjected to transient periods of ischemia of 30, 45, 60, 75, 90, 105, o
r 120 minutes, respectively, by increasing the intraocular pressure (I
OP) of the left eye above systolic values, Five, 7, 14, and 30 days la
ter, the rats were killed, and their retinas were prepared as whole mo
unts for examination under fluorescence microscopy to estimate RGC sur
vival. Results. The authors found that periods of ischemia of 30 and 4
5 minutes do not induce RGC death; longer periods of transient ischemi
a induce the death of a proportion of RGCs, and the proportion increas
es with the duration of the ischemia; RGC death, which can be observed
as early as 5 days after ischemia, continues during die 30-day study
period; and periods of ischemia that last 90 minutes or more cause the
death of approximately 95% of tile RGC population 30 days later, Conc
lusions. Increases of the IOP above systolic levels for periods of 60
minutes or more result in RGC loss in the rat retina. Both the duratio
n of the initial transient period of ischemia and the duration of the
survival period influence the proportion of RGC death.