Rabbit corneas were perfused in vitro with an irrigation solution for
90 minutes. This was followed by 6 hours of perfusion with tissue cult
ure medium TC199 during which endothelial function was assessed by mon
itoring rates of swelling during a period of perfusion in the absence
of bicarbonate ions, and subsequent rates of thinning when bicarbonate
ions were restored to the perfusate. Corneal thickness (measured with
an ultrasonic pachymeter) immediately following excision was 401 I-lm
(SD 19, n = 23). During the 90 minute perfusion at 35 degrees C, corn
eas exposed to balanced salt solution (BSS), Hartmann's solution or 0.
9% NaCl (all initially at room temperature) swelled, respectively, at
14 (SD 2.3, n = 4), 11 (SD 2.6, n = 4), and 70 (SD 4.3, n = 4) mu m/h.
Cold Hartmann's solution (initially at 4 degrees C) caused corneas to
swell at 9 (SD 2.3, n = 4) mu m/h. On the other hand, corneas perfuse
d with BSS Plus thinned at 9 (SD 3.4, n = 4) mu m/h and TC199 with Ear
le's salts had little effect on thickness. Rates of swelling and thinn
ing during the following assessment perfusion showed no apparent effec
ts of prior exposure to any of the irrigation solutions on the barrier
properties or pump function of the endothelium. Despite this, the inc
reased thickness of corneas exposed initially to BSS, cold Hartmann's
solution, or 0.9% NaCl was not fully reversed, even by the end of the
6 hour assessment perfusion. In contrast, the swelling observed in cor
neas exposed to Hartmann's solution at room temperature was reversed a
nd these corneas had returned to their normal thickness by the end of
the assessment period. All corneas, even those exposed to 0.9% NaCl, h
ad an intact endothelial mosaic with no evidence of damage or cell los
s, although morphological differences in cell shape and the appearance
of cell borders were evident compared with freshly isolated cornea.