Pa. Hamblin et al., SUB NANOMOLAR CONCENTRATIONS OF CIGUATOXIN-1 EXCITE PREGANGLIONIC TERMINALS IN GUINEA-PIG SYMPATHETIC-GANGLIA, Naunyn-Schmiedeberg's archives of pharmacology, 352(2), 1995, pp. 236-246
The actions of low concentrations of ciguatoxin-1 (CTX-1, 0.2-0.8 nM)
in guinea-pig sympathetic ganglia have been analysed using intracellul
ar recording techniques in vitro. The effects of CTX-1 were graded wit
h concentration but sensitivity varied markedly between neurones in th
e same preparation. Other than an initial transient ( similar to 10 mi
n) depolarization of some ganglion cells accompanied by an increase in
input resistance, passive electrical properties did not significantly
differ from controls. Amplitude and threshold of action potentials ev
oked by depolarizing current and threshold, latency and form of the in
itial responses to nerve stimulation were also not affected. Exposure
to CTX-1 generated marked increases in the frequency of spontaneous ex
citatory synaptic potentials which often occurred in bursts (15-66 Hz)
of similar amplitudes. Single stimuli to incoming nerves produced rep
etitive synaptic responses arising from preganglionic, but not from pe
ripheral afferent, axons. Following brief ( < 5 min) exposure to CTX-1
, these effects declined over 30 min but, after longer exposure ( > 15
min), they persisted for several hours despite continuous washing. Al
l activity generated by CTX-1 was significantly reduced or abolished b
y d-tubocurarine (10(-5)-10(-4) M), hexamethonium (10(-5) M), tetrodot
oxin (10(-7)-10(-6) M), omega-conotoxin (10(-7) M), reduced Ca2+ (0.1
m/M)/raised Mg2+ (10 mM), raised Ca2+ (6 mM) or raised Mg2+ (25 mM). T
he data suggest that CTX-1 activates preganglionic axons by modifying
the voltage sensitivity of a subpopulation of Na+ channels. Effects on
these unmyelinated axons occur at much lower concentrations than have
been reported to affect myelinated ones. Many of the symptoms of cigu
atera poisoning might be explained by activity in autonomic and perhap
s other unmyelinated nerve terminals.