THE PHOSPHOLIPASE-A(2) INHIBITOR BROMOPHENACYL BROMIDE PREVENTS THE DEPOLARIZATION-INDUCED INCREASE IN [H-3] AMPA BINDING IN RAT-BRAIN SYNAPTONEUROSOMES
J. Bernard et al., THE PHOSPHOLIPASE-A(2) INHIBITOR BROMOPHENACYL BROMIDE PREVENTS THE DEPOLARIZATION-INDUCED INCREASE IN [H-3] AMPA BINDING IN RAT-BRAIN SYNAPTONEUROSOMES, Brain research, 628(1-2), 1993, pp. 340-344
We previously demonstrated that potassium (KCl)-induced depolarization
of synaptoneurosomes prepared from rat telencephalon increased H-3]am
ino-3-hydroxy-5-methylisoxazole-4-propionate ([H-3]AMPA) binding to th
e AMPA receptor. In the present study, we determined the effects of in
hibitors of various calcium-dependent enzymes on this response to depo
larization. Treatment of intact synaptoneurosomes with the phospholipa
se A2 (PLA2) inhibitor, bromophenacyl bromide (BPB), produced a marked
and dose-dependent reduction in KCl-induced enhancement in [H-3]AMPA
binding. BPB had no significant effect on [H-3]TPP accumulation in int
act synaptoneurosomes, an index of membrane depolarization. In contras
t to BPB, inhibitors of calcium-dependent kinases and proteases did no
t reduced the KCl-induced increase in [H-3]AMPA binding. The results s
trengthen the hypothesis that phospholipase-induced modifications of A
MPA receptor properties may be an important component of synaptic plas
ticity.