Sensorimotor learning allows organisms to interact adaptively with their environment, yet a detailed description of how sensory input modifies motor circuitry during learning has not been developed. Since many movement disorders involve dysfunction of motor planning and disruption of learned motor programs, understanding how motor programs are instantiated in motor circuits during learning is essential. Vocal learning in songbirds is a particularly tractable model of sensorimotor learning since birdsong is an ethological and readily quantifiable behavior, and because the neuroanatomical substrates of song production are identified and accessible. Song learning entails the convergence of juvenile song toward a tutor song, and although changes in song are associated with changes in premotor nuclei, the synaptic and cellular plasticity mechanisms underlying song learning remain unknown. This proposal describes experiments that will combine a form of rapid song learning with chronic in vivo electrophysiology in behaving animals to identify patterns of premotor activity that accompany changes in song, and utilize in vitro whole-cell recording and minimal stimulation to identify the synaptic loci and mechanisms of this plasticity. Results from these experiments will provide an integrated and comprehensive account of vocal motor learning, from synaptic plasticity to changes in circuit dynamics to altered vocal behavior, and thereby give broad insight into how the nervous system learns adaptive and complex behaviors.

Public Health Relevance

The experiments in this proposal will elucidate the detailed changes in brain circuitry that underlie learning of a complex motor task. Many neurological disorders involve dysfunction of brain circuits that control motor behavior, and understanding how motor behavior is encoded by neurons in motor circuits would provide important insight into how these circuits produce disrupted behaviors in disease states.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32NS073284-01A1
Application #
8203108
Study Section
Special Emphasis Panel (ZRG1-F02B-M (20))
Program Officer
Chen, Daofen
Project Start
2011-08-01
Project End
2014-07-31
Budget Start
2011-08-01
Budget End
2012-07-31
Support Year
1
Fiscal Year
2011
Total Cost
$51,326
Indirect Cost
Name
University of California San Francisco
Department
Physiology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143