The purpose of this study was to determine the role of protein kinase
C (PKC) isozymes in carbachol-induced protein secretion in the lacrima
l gland. Three isoforms of PKC are present in rat lacrimal gland: PKC-
alpha, -delta and -epsilon. Carbachol translocated PKC-epsilon during
5 s incubation. Pretreatment with PdBu for 0 to 4 h down-regulated PKC
-alpha by 31% at 20 min, PKC-epsilon by 36% at 2 h, and PKC-delta by 3
7% at 4 h. A 2 h phorbol ester treatment inhibited carbachol-induced s
ecretion completely at 1 min and partially at 5, and 20 min, but did n
ot alter the carbachol-induced increase in the intracellular [Ca2+]. W
e conclude that PKC-alpha. and -epsilon, but not PKC-delta, are implic
ated in cholinergic agonist-induced protein secretion in rat lacrimal
gland.