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Short Bouts of Vocalization Induce Long-lasting Fast γ Oscillations in a Sensorimotor Nucleus

Overview
Journal J Neurosci
Specialty Neurology
Date 2011 Sep 30
PMID 21957255
Citations 12
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Abstract

Performance evaluation is a critical feature of motor learning. In the vocal system, it requires the integration of auditory feedback signals with vocal motor commands. The network activity that supports such integration is unknown, but it has been proposed that vocal performance evaluation occurs offline. Recording from NIf, a sensorimotor structure in the avian song system, we show that short bouts of singing in adult male zebra finches (Taeniopygia guttata) induce persistent increases in firing activity and coherent oscillations in the fast gamma range (90-150 Hz). Single units are strongly phase locked to these oscillations, which can last up to 30 s, often outlasting vocal activity by an order of magnitude. In other systems, oscillations often are triggered by events or behavioral tasks but rarely outlast the event that triggered them by more than 1 s. The present observations are the longest reported gamma oscillations triggered by an isolated behavioral event. In mammals, gamma oscillations have been associated with memory consolidation and are hypothesized to facilitate communication between brain regions. We suggest that the timing and persistent nature of NIf's fast gamma oscillations make them well suited to facilitate the integration of auditory and vocal motor traces associated with vocal performance evaluation.

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References
1.
Williams H, Vicario D . Temporal patterning of song production: participation of nucleus uvaeformis of the thalamus. J Neurobiol. 1993; 24(7):903-12. DOI: 10.1002/neu.480240704. View

2.
Coleman M, Mooney R . Synaptic transformations underlying highly selective auditory representations of learned birdsong. J Neurosci. 2004; 24(33):7251-65. PMC: 6729779. DOI: 10.1523/JNEUROSCI.0947-04.2004. View

3.
Cardin J, Schmidt M . Noradrenergic inputs mediate state dependence of auditory responses in the avian song system. J Neurosci. 2004; 24(35):7745-53. PMC: 6729633. DOI: 10.1523/JNEUROSCI.1951-04.2004. View

4.
Keller G, Hahnloser R . Neural processing of auditory feedback during vocal practice in a songbird. Nature. 2008; 457(7226):187-90. DOI: 10.1038/nature07467. View

5.
Dave A, Margoliash D . Song replay during sleep and computational rules for sensorimotor vocal learning. Science. 2000; 290(5492):812-6. DOI: 10.1126/science.290.5492.812. View