H. Golan et al., ANALYSIS OF EVOKED AND SPONTANEOUS QUANTAL RELEASE AT HIGH-PRESSURE IN CRUSTACEAN EXCITATORY SYNAPSES, Pflugers Archiv, 430(5), 1995, pp. 617-625
The cellular mechanisms underlying the effect of high pressure on syna
ptic transmission were studied in the opener muscle of the lobster wal
king leg. Excitatory postsynaptic currents (EPSCs) were recorded using
a loose macropatch-clamp technique at normal pressure and 3.5, 6.9 MP
a helium pressure. Responses of the single excitatory axon could be gr
ouped into two types: low-yield (L) synapses exhibiting small EPSCs wi
th a considerable number of failures, and high-yield (H) synapses havi
ng larger EPSCs with very few failures. High pressure reduced the aver
age EPSC amplitude in all synapses and shifted their amplitude histogr
ams to the left by decreasing the quantal content (m) without changing
their quantum current (q). A binomial distribution fit of EPSC amplit
udes revealed that high pressure greatly decreased n, the number of av
ailable active zones, but the effect on p, the probability of release
for each zone, was not consistent. Many of the spontaneous miniature E
PSCs (mEPSCs), observed only in L-type synapses, were ''giant'' (size
= 2-5 q). High pressure increased the frequency of the giant mEPSCs bu
t had little effect on their amplitude histogram. High pressure depres
sed evoked synaptic transmission by modulating the presynaptic quantal
release parameters, but concomitantly enhanced spontaneous quantal re
lease by an unknown mechanism.