Bath-applied glutamate (10-1000 mu M) produced excitatory and inhibito
ry responses on numerous identified neurons of the mollusc Lymnaea sta
gnalis. Using both in situ and in vitro preparations, glutamate or glu
tamate agonists produced a depolarization in identified neurons right
pedal dorsal 1 and right pedal dorsal 2 and 3. However, attempts to bl
ock glutamate-evoked responses with glutamate antagonists were unsucce
ssful. We examined a potential glutamatergic neuron, visceral dorsal 4
. Exogenous application of the peptides (GDPFLRFamide and SDPFLRFamide
) could mimic the inhibitory, but not the excitatory effects of viscer
al dorsal 4 on its postsynaptic cells, implying the presence of a seco
nd transmitter. We tested the possibility that glutamate is this secon
d neurotransmitter by using excitatory synapses between visceral dorsa
l 4 and postsynaptic cells right pedal dorsal 2 and 3, right pedal dor
sal 1, visceral F group and right parietal B group neurons. Of all the
putative neurotransmitters tested, only glutamate had consistent exci
tatory effects on these postsynaptic cells. Also, the amplitude of the
right pedal dorsal 2 and 3 excitatory postsynaptic potentials was red
uced in the presence of N-methyl-D-aspartate and other glutamate agoni
sts, suggesting desensitization of the endogenous transmitter receptor
. In conclusion, some identified Lymnaea neurons respond to glutamate
via a receptor with novel pharmacological properties. Furthermore, a L
ymnaea interneuron may employ glutamate as a transmitter at excitatory
synapses. Copyright (C) 1996 IBRO. Published by Elsevier Science Ltd.