Abstract

Among insect GABA receptors, the GABA-gated chloride channel subtype is insensitive to bicuculline and has been thought to be composed of two populations because of differences in chloride conductance increase, GABA and picrotoxin (PTX) sensitivity. To characterize this possible diversity in GABA-gated chloride channels, electropharmacological experiments were performed on giant interneuron synaptic GABA receptors and on somatic GABA receptors of dorsal unpaired median (DUM) neuron and fast coxal depressor (Df) motoneuron of the cockroach Periplaneta americana (L). Electrophysiological assays performed at cercal-afferent giant interneuron synapses demonstrated that a biphasic increase in membrane conductance, in response to long-lasting (30 s) neuropilar microapplication of GABA, could be explained by the existence of two GABA-operated chloride channel receptor subtypes. The low stable membrane conductance increase, representing less than 30% of the maximum reached during the early transient phase, was not desensitized quickly. It was reproduced by neuropilar microapplication of cis-4-aminocrotonic acid (CACA) and, in contrast to the fast phase, was not antagonized by bath application of 10−5 M PTX. Long-lasting (3 min) pneumatic pressure application of GABA on the cell body of motoneuron Df evoked a fast transient hyperpolarization followed by a slower phase of further hyperpolarization. PTX (10−5 M) blocked the fast transient phase and revealed a slow stable hyperpolarization. PTX (10−4 M) blocked the major part of the remaining GABA response. The slow hyperpolarization was reproduced by application of CACA. Similar effects of GABA and CACA were recorded on DUM neuron cell bodies. All of these observations are consistent with the possible existence of two GABA-gated chloride channel subtypes in the insect CNS. © 1999 Society of Chemical Industry

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