|
|
||||||||
1McGovern Institute and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts; and 2Department of Physics and Department of Psychology, Pennsylvania State University, University Park, Pennsylvania
Submitted 6 September 2006; accepted in final form 16 December 2006
High vocal center (HVC) is part of the premotor pathway necessary for song production and is also a primary source of input to the anterior forebrain pathway (AFP), a basal ganglia-related circuit essential for vocal learning. We have examined the activity of identified HVC neurons of zebra finches during singing. Antidromic activation was used to identify three classes of HVC cells: neurons projecting to the premotor nucleus RA, neurons projecting to area X in the AFP, and putative HVC interneurons. HVC interneurons are active throughout the song and display tonic patterns of activity. Projection neurons exhibit highly phasic stereotyped firing patterns. X-projecting (HVC(X)) neurons burst zero to four times per motif, whereas RA-projecting neurons burst extremely sparselyat most once per motif. The bursts of HVC projection neurons are tightly locked to the song and typically have a jitter of <1 ms. Population activity of interneurons, but not projection neurons, was significantly correlated with syllable patterns. Consistent with the idea that HVC codes for the temporal order in the song rather than for sound, the vocal dynamics and neural dynamics in HVC occur on different and uncorrelated time scales. We test whether HVC(X) neurons are auditory sensitive during singing. We recorded the activity of these neurons in juvenile birds during singing and found that firing patterns of these neurons are not altered by distorted auditory feedback, which is known to disrupt learning or to cause degradation of song already learned.
This article has been cited by other articles:
![]() |
M. H. Kao, B. D. Wright, and A. J. Doupe Neurons in a Forebrain Nucleus Required for Vocal Plasticity Rapidly Switch between Precise Firing and Variable Bursting Depending on Social Context J. Neurosci., December 3, 2008; 28(49): 13232 - 13247. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. R. Griff, M. Mafhouz, A. Perrut, and M. A. Chaput Comparison of Identified Mitral and Tufted Cells in Freely Breathing Rats: I. Conduction Velocity and Spontaneous Activity Chem Senses, November 1, 2008; 33(9): 779 - 792. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. T. Sakata and M. S. Brainard Online Contributions of Auditory Feedback to Neural Activity in Avian Song Control Circuitry J. Neurosci., October 29, 2008; 28(44): 11378 - 11390. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. F. Roberts, M. E. Klein, M. F. Kubke, J. M. Wild, and R. Mooney Telencephalic Neurons Monosynaptically Link Brainstem and Forebrain Premotor Networks Necessary for Song J. Neurosci., March 26, 2008; 28(13): 3479 - 3489. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Thompson, W. Wu, R. Bertram, and F. Johnson Auditory-Dependent Vocal Recovery in Adult Male Zebra Finches Is Facilitated by Lesion of a Forebrain Pathway That Includes the Basal Ganglia J. Neurosci., November 7, 2007; 27(45): 12308 - 12320. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Meitzen, I. T. Moore, K. Lent, E. A. Brenowitz, and D. J. Perkel Steroid Hormones Act Transsynaptically within the Forebrain to Regulate Neuronal Phenotype and Song Stereotypy J. Neurosci., October 31, 2007; 27(44): 12045 - 12057. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Person and D. J. Perkel Pallidal Neuron Activity Increases during Sensory Relay through Thalamus in a Songbird Circuit Essential for Learning J. Neurosci., August 8, 2007; 27(32): 8687 - 8698. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |