Journal of Neuroscience, Vol 8, 2748-2757, Copyright © 1988 by Society for Neuroscience
Presynaptic inhibition of identified wind-sensitive afferents in the cercal system of the locust
GS Boyan
Molecular Neurobiology Group, Research School of Biological Sciences, Australian National University, Canberra City.
The paired cerci located at the tip of the locust abdomen bear a large
number of wind-sensitive filiform hairs, each of which sends an axon via
the cercal nerve into the terminal ganglion of the CNS. The filiform
afferents fire bursts of action potentials when their hairs are displaced
by wind or mechanical stimuli. Filiform axon terminals in the CNS are
depolarized concomitantly with the discharge of another type of unit (a
primary afferent-depolarizing, or PAD, unit) recorded in the cercal nerve.
The instantaneous spike frequency of PAD unit discharges matches the evoked
depolarization very closely, and during such depolarizations spike
amplitudes in the filiform afferent terminals are reduced by up to 55%.
Depolarizing current pulses injected into the axonal terminals of an
identified filiform afferent evoke spikes that are blocked by the PAD unit,
probably via an intercalated interneuron. The PAD unit makes a monosynaptic
connection with only one of the 4 giant interneurons (GIN 2) on each side
of the terminal ganglion, and indirect connections with 2 others.
Depolarizing current pulses injected into the neuropilar segments of GINs
evoke fewer spikes when the PAD unit is active, consistent with the PAD
unit's mediation of conductance changes in postsynaptic cells.
Iontophoretic injection of Lucifer yellow shows the PAD unit to be an
afferent with axon terminals overlapping those of filiform afferents and
posteriorly directed branches of interneurons such as GIN 2 in the CNS.
Passive movements of a cercus, monitored with a position transducer, show
that the PAD unit fires discrete bursts during cercal displacement. The PAD
unit most probably has its soma and dendrites in tissue spanning the cercal
base. By responding to cercal movements sufficient to also activate
filiform hairs, and by mediating conductance changes in both the
presynaptic terminals of filiform afferents and the postsynaptic membranes
of interneurons, the PAD unit desensitizes a pathway to movement-generated
afferent input, and ensures that the locust remains sensitive to external
wind stimuli.