Changes in the activity of the enzyme protein kinase C (PKC) have been
implicated in learning and memory consolidation, and in the induction
of long-term potentiation. The precise role of PKC in memory processi
ng is still unknown. Using 1-day-old chicks trained on a single-trial
passive avoidance task, we demonstrate that inhibition of PKC activity
by melittin induced retention loss, in a dose-dependent manner, in th
e second stage of a three-stage sequence of memory processing. The eff
ect was lateralized to the left hemisphere of the chick forebrain. Thi
s effect of melittin was prevented by high concentrations (16-320 mu M
) of the PKC activator, phorbol 12-myristate 13-acetate (PMA). Further
more, concentrations of PMA in the range 1.6 to 40 mu M were shown to
induce long-term memory consolidation following a weakly reinforced ve
rsion of the learning task, which normally does not lead to formation
of longterm memory. That these actions of PMA are attributable to PKC
activation is supported by the further finding that the inactive phorb
ol ester 4 alpha-PDD had no effect either on melittin-induced amnesia
or on memory consolidation following weakly reinforced learning. Parad
oxically, concentrations of 16 mu M or higher of PMA inhibited memory
consolidation for the normal strongly reinforced learning trial, an ef
fect again not observed with 40 alpha-PDD. The results are consistent
with the view that PKC activity may be implicated in a pre-long-term s
tage of memory processing.