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Research ArticleNew Research, Cognition and Behavior

Dopamine Depletion Affects Vocal Acoustics and Disrupts Sensorimotor Adaptation in Songbirds

Varun Saravanan, Lukas A. Hoffmann, Amanda L. Jacob, Gordon J. Berman and Samuel J. Sober
eNeuro 24 May 2019, 6 (3) ENEURO.0190-19.2019; https://doi.org/10.1523/ENEURO.0190-19.2019
Varun Saravanan
1Neuroscience Graduate Program, Graduate Division of Biological and Biomedical Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322
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Lukas A. Hoffmann
1Neuroscience Graduate Program, Graduate Division of Biological and Biomedical Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322
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Amanda L. Jacob
2Department of Biology, Emory University, Atlanta, GA 30322
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Gordon J. Berman
2Department of Biology, Emory University, Atlanta, GA 30322
3Department of Physics, Emory University, Atlanta, GA 30322
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Samuel J. Sober
2Department of Biology, Emory University, Atlanta, GA 30322
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Abstract

Dopamine is hypothesized to convey error information in reinforcement learning tasks with explicit appetitive or aversive cues. However, during motor skill learning feedback signals arise from an animal’s evaluation of sensory feedback resulting from its own behavior, rather than any external reward or punishment. It has previously been shown that intact dopaminergic signaling from the ventral tegmental area/substantia nigra pars compacta (VTA/SNc) complex is necessary for vocal learning when songbirds modify their vocalizations to avoid hearing distorted auditory feedback (playbacks of white noise). However, it remains unclear whether dopaminergic signaling underlies vocal learning in response to more naturalistic errors (pitch-shifted feedback delivered via headphones). We used male Bengalese finches (Lonchura striata var. domestica) to test the hypothesis that the necessity of dopamine signaling is shared between the two types of learning. We combined 6-hydroxydopamine (6-OHDA) lesions of dopaminergic terminals within Area X, a basal ganglia nucleus critical for song learning, with a headphones learning paradigm that shifted the pitch of auditory feedback and compared their learning to that of unlesioned controls. We found that 6-OHDA lesions affected song behavior in two ways. First, over a period of days lesioned birds systematically lowered their pitch regardless of the presence or absence of auditory errors. Second, 6-OHDA lesioned birds also displayed severe deficits in sensorimotor learning in response to pitch-shifted feedback. Our results suggest roles for dopamine in both motor production and auditory error processing, and a shared mechanism underlying vocal learning in response to both distorted and pitch-shifted auditory feedback.

  • basal ganglia
  • Bengalese finch
  • dopamine
  • sensorimotor adaptation
  • songbird
  • vocal learning

Footnotes

  • The authors declare no competing financial interests.

  • This work was supported by National Institutes of Health (NIH) National Institute of Neurologic Disorders and Stroke Grants F31 NS100406 and R01 NS084844, the NIH National Institute of Biomedical Imaging and Bioengineering Grant R01EB022872, the NIH National Institute of Mental Health Grant R01 MH115831-01, the National Science Foundation Grant 1456912, and by Emory’s Udall Center of Excellence for Parkinson’s Disease Research.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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Dopamine Depletion Affects Vocal Acoustics and Disrupts Sensorimotor Adaptation in Songbirds
Varun Saravanan, Lukas A. Hoffmann, Amanda L. Jacob, Gordon J. Berman, Samuel J. Sober
eNeuro 24 May 2019, 6 (3) ENEURO.0190-19.2019; DOI: 10.1523/ENEURO.0190-19.2019

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Dopamine Depletion Affects Vocal Acoustics and Disrupts Sensorimotor Adaptation in Songbirds
Varun Saravanan, Lukas A. Hoffmann, Amanda L. Jacob, Gordon J. Berman, Samuel J. Sober
eNeuro 24 May 2019, 6 (3) ENEURO.0190-19.2019; DOI: 10.1523/ENEURO.0190-19.2019
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Keywords

  • basal ganglia
  • Bengalese finch
  • dopamine
  • sensorimotor adaptation
  • songbird
  • vocal learning

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