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The role of NIf in the generation of sleep-related burst sequences in HVC
Richard Hahnloser, Alexay Kozhevnikov, and Michale Fee
Bell Labs Lucent Technologies
We have recently shown that premotor burst activity in nucleus RA of
the zebra finch is directly driven by RA-projecting HVC neurons
(HVC(RA)), each of which bursts at a single precise time in the song
motif, and as a population burst throughout the song. This explicit
representation of time has also been observed to underlie the
generation of RA burst sequences during sleep. To understand the
origin of the time representation in HVC, we are investigating the
role of premotor inputs to HVC. Injections of lidocaine or muscimol
into premotor nucleus Uvaeformis (Uva) in the sleeping bird resulted
in a 2-3 fold increase in the rate of sleep-bursts in HVC. In
contrast, injections into premotor Nucleus Interface (NIf) completely
and reversibly abolished sleep-burst activity in HVC. Antidromically
identified HVC-projecting NIf (NIf(HVC)) neurons generate dense
patterns of bursts; during sleep a fraction of these bursts are highly
correlated with subsequent bursts in HVC(RA) neurons. This result
suggests that during singing, NIf(HVC) neurons will likewise generate
dense patterns of bursts, some fraction of which will be tightly
locked to the song vocalization. This prediction is being tested by
recording identified NIf neurons in the singing bird. Furthermore,
robust activation of the HVC neuron populations by electrical
stimulation in RA or X has only a transient effect on song output
(~20ms). Thus we suggest that the HVC time code originates from
dynamics in NIf, is transmitted to HVC in a temporally dense code, and
that the sparseness of the HVC time representation results from
network or biophysical properties within HVC.