The long-term objectives of this project are to elucidate the neural and hormonal bases of learned vocal behavior in passerine birds. Birds must hear an external auditory model during a restricted period of development in order to subsequently form an accurate vocal copy of that pattern. Exposure to conspecific vocal sounds beyond this """"""""sensitive period"""""""" is of little or no value for vocal learning. We have previously provided evidence for additional, separate sensitive periods during vocal development. For example, lesions of a specific neural circuit disrupt vocal behavior in young birds during vocal learning, but have no effect on song production in older juveniles and adults. Thus, there is a """"""""learning circuit"""""""" in the forebrain that is involved with vocal development during a restricted period, but not with subsequent maintenance of stereotyped vocal patterns. In addition, we have shown that there are also sensitive periods when circulating hormone levels must be at specific levels in order for vocal learning to develop normally. We would like to investigate the factors that regulate these and other sensitive periods during vocal learning in order to begin to elucidate the cellular mechanisms by which organisms learn to communicate vocally. Experiments to be conducted include the following: (1) Does blocking the action of hormones extend the sensitive period for the effect of lesions in the learning circuit of the forebrain? (2) What are the exact times during development when altered hormone levels (either too high or too low, respectively) disrupt vocal learning? We anticipate that periods requiring low vs. high hormone levels may be non-overlapping, and correlate with distinct aspects of vocal learning. (3) We will selectively lesion different levels of the learning circuit as well as brain regions known to be important for adult vocal production at different times during vocal development in order to assess their contribution to behavior at different stages of learning. (4) Lesions at one level of the learning circuit induce neuronal death in adjacent levels of this circuit only in juvenile birds during vocal learning, but not in adults. We will begin to investigate the role of target factors and afferent inputs in this induced cell death during vocal learning. (5) Neurogenesis continues throughout the life span in songbirds, and new neurons are incorporated into neural circuits for vocal learning at an enhanced rate during song development. We will determine whether this neuronal addition is due to enhanced cellular proliferation in the forebrain during vocal development. (6) We will determine whether there is a sensitive period for reliance on auditory feedback of self-produced vocalizations during vocal development. These experiments will bear importantly on hypotheses for neural and endocrine mechanisms of vocal learning in humans, and may have important implications for problems of vocal perception and production in humans such as stuttering and dyslexia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS037547-19
Application #
2892411
Study Section
Psychobiology, Behavior, and Neuroscience Review Committee (PBN)
Program Officer
Edwards, Emmeline
Project Start
1986-12-01
Project End
2001-01-31
Budget Start
1999-08-01
Budget End
2001-01-31
Support Year
19
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Southern California
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Achiro, Jennifer M; Shen, John; Bottjer, Sarah W (2017) Neural activity in cortico-basal ganglia circuits of juvenile songbirds encodes performance during goal-directed learning. Elife 6:
Achiro, Jennifer M; Bottjer, Sarah W (2013) Neural representation of a target auditory memory in a cortico-basal ganglia pathway. J Neurosci 33:14475-88
Yip, Zhiqi C; Miller-Sims, Vanessa C; Bottjer, Sarah W (2012) Morphology of axonal projections from the high vocal center to vocal motor cortex in songbirds. J Comp Neurol 520:2742-56
Miller-Sims, Vanessa C; Bottjer, Sarah W (2012) Auditory experience refines cortico-basal ganglia inputs to motor cortex via remapping of single axons during vocal learning in zebra finches. J Neurophysiol 107:1142-56
Bottjer, Sarah W; To, Michelle (2012) Afferents from vocal motor and respiratory effectors are recruited during vocal production in juvenile songbirds. J Neurosci 32:10895-906
Miller-Sims, Vanessa C; Bottjer, Sarah W (2012) Development of auditory-vocal perceptual skills in songbirds. PLoS One 7:e52365
Bottjer, Sarah W; Altenau, Brie (2010) Parallel pathways for vocal learning in basal ganglia of songbirds. Nat Neurosci 13:153-5
Reiner, Anton; Laverghetta, Antonio V; Meade, Christopher A et al. (2004) An immunohistochemical and pathway tracing study of the striatopallidal organization of area X in the male zebra finch. J Comp Neurol 469:239-61
Zevin, Jason D; Seidenberg, Mark S; Bottjer, Sarah W (2004) Limits on reacquisition of song in adult zebra finches exposed to white noise. J Neurosci 24:5849-62
Iyengar, Soumya; Bottjer, Sarah W (2002) Development of individual axon arbors in a thalamocortical circuit necessary for song learning in zebra finches. J Neurosci 22:901-11

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