PURPOSE. These studies were performed to characterize the voltage-gate
d, whole-cell ionic currents in rabbit bulbar conjunctival epithelial
and goblet cells. METHODS. New Zealand White rabbits were killed, and
the bulbar conjunctiva was isolated. Conjunctival cells were dissociat
ed for patch clamp analysis of whole-cell currents. The amphotericin,
perforated-patch, whole-cell technique was used. RESULTS. Conjunctival
epithelial cells had a mean capacitance of 6.72 pF (SE = 0.49; n = 25
). The primary currents found were an inwardly rectifying K+ current,
a saturating K+ current, and an outwardly rectifying nonselective cati
on current. A second nonselective cation current also appeared to be p
resent. The inward current was observed in a KCl Ringer's bath and was
almost nonexistent in a NaCl bath. The current was Ba2+- and Cs+-sens
itive. The second K+ current became saturated at depolarized voltages
and was Ba2+- and quinidine-sensitive. The first outward nonselective
cation current was typically less than 100 pA in amplitude and activat
ed at voltages positive to 0 mV. Tail current experiments showed that
the current was cation selective. The current was blocked by Gd3+ but
not by the Cl- current blockers 4,4'-diisothiocyanostilbene-2,2'-disul
fonic acid or 5-nitro-2-(3-phenylpropylamino)benzoic acid. The second
nonselective cation current was larger and Gd3+-insensitive. The prima
ry current observed in goblet cells was a large outward K+ current. CO
NCLUSIONS. The primary currents observed during whole-cell patch clamp
ing of bulbar conjunctival epithelium are a Ba2+- and Cs+-sensitive, i
nwardly rectifying K+ current, a saturating K+ current, and two outwar
dly rectifying nonselective cation currents. Goblet cells contain a la
rge outward K+ current.