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The Journal of Neurophysiology Vol. 81 No. 6 June 1999, pp. 3007-3020
Copyright ©1999 by the American Physiological Society
Department of Neurobiology, Duke University Medical Center, Durham, North Carolina 27710
Spiro, John E.,
Matthew B. Dalva, and
Richard Mooney.
Long-Range Inhibition Within the Zebra Finch Song Nucleus RA Can
Coordinate the Firing of Multiple Projection Neurons. J. Neurophysiol. 81: 3007-3020, 1999.
Long-range inhibition within the zebra finch song nucleus RA can
coordinate the firing of multiple projection neurons. The zebra finch forebrain song control nucleus RA (robust nucleus of the
archistriatum) generates a phasic and temporally precise neural signal
that drives vocal and respiratory motoneurons during singing. RA's
output during singing predicts individual notes, even though afferent
drive to RA from the song nucleus HVc is more tonic, and predicts song
syllables, independent of the particular notes that comprise the
syllable. Therefore RA's intrinsic circuitry transforms neural
activity from HVc into a highly precise premotor output. To understand
how RA's intrinsic circuitry effects this transformation, we
characterized RA interneurons and projection neurons using
intracellular recordings in brain slices. RA interneurons fired fast
action potentials with steep current-frequency relationships and had
small somata with thin aspinous processes that extended throughout
large portions of the nucleus; the similarity of their fine processes
to those labeled with a glutamic acid decarboxylase (GAD) antibody
strongly suggests that these interneurons are GABAergic. Electrical
stimulation revealed that RA interneurons receive excitatory inputs
from RA's afferents, the lateral magnocellular nucleus of the anterior
neostriatum (LMAN) and HVc, and from local axon collaterals of RA
projection neurons. To map the functional connections that RA
interneurons make onto RA projection neurons, we focally uncaged
glutamate, revealing long-range inhibitory connections in RA. Thus
these interneurons provide fast feed-forward and feedback inhibition to
RA projection neurons and could help create the phasic pattern of
bursts and pauses that characterizes RA output during singing.
Furthermore, selectively activating the inhibitory network phase locks
the firing of otherwise unconnected pairs of projection neurons,
suggesting that local inhibition could coordinate RA output during singing.
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