E. Pearstein et al., CRAYFISH SENSORY TERMINALS AND MOTOR-NEURONS EXHIBIT 2 DISTINCT TYPESOF GABA RECEPTORS, Journal of comparative physiology. A, Sensory, neural, and behavioral physiology, 180(1), 1997, pp. 71-79
Motor neurones of the crayfish walking system display inhibitory respo
nses evoked either by gamma-amino butyric acid (GABA) or glutamate, po
ssibly involving the same receptor (Pearlstein et al. 1994). In order
to test if this sensibility to both GABA and glutamate was a specific
property of crayfrsh GABA receptors, pharmacological characteristics o
f GABA-evoked responses in both sensory terminals from CB chordotonal
organ and motor neurones of the walking system have been compared. Bot
h receptors are GABA-gated Cl- channels activated by specific GABA(A)
(muscimol, isoguvacine), GABA(B) (3-aminopropyl phosphinic acid), and
GABA(C) (cis-4-amino crotonic acid) agonists, and blocked by competiti
ve (beta-guanidino propionic acid) and non-competitive (picrotoxin) an
tagonists. They were insensitive to specific GABA(A) (bicuculline, SR-
95531) and GABA(B) (phaclofen) antagonists. Furthermore, in both cases
, nipecotic acid and the modulatory drug diazepam had no effect. Howev
er, our results demonstrate that GABA receptors of sensory terminals a
re different from those of motor neurones. GABA-induced desensitisatio
n only occurred in sensory terminals. Moreover, glutamate was shown to
activate GABA-gated Cl- channels in motor neurones, but not in sensor
y terminals. Therefore, GABA is likely to be the endogenous neurotrans
mitter of presynaptic inhibition in sensory terminals, whereas inhibit
ion between antagonistic motor neurones would be achieved by glutamate
.