Literature DB >> 20484651

Singing-related neural activity distinguishes two putative pallidal cell types in the songbird basal ganglia: comparison to the primate internal and external pallidal segments.

Jesse H Goldberg1, Avital Adler, Hagai Bergman, Michale S Fee.   

Abstract

The songbird area X is a basal ganglia homolog that contains two pallidal cell types-local neurons that project within the basal ganglia and output neurons that project to the thalamus. Based on these projections, it has been proposed that these classes are structurally homologous to the primate external (GPe) and internal (GPi) pallidal segments. To test the hypothesis that the two area X pallidal types are functionally homologous to GPe and GPi neurons, we recorded from neurons in area X of singing juvenile male zebra finches, and directly compared their firing patterns to neurons recorded in the primate pallidus. In area X, we found two cell classes that exhibited high firing (HF) rates (>60 Hz) characteristic of pallidal neurons. HF-1 neurons, like most GPe neurons we examined, exhibited large firing rate modulations, including bursts and long pauses. In contrast, HF-2 neurons, like GPi neurons, discharged continuously without bursts or long pauses. To test whether HF-2 neurons were the output neurons that project to the thalamus, we next recorded directly from pallidal axon terminals in thalamic nucleus DLM, and found that all terminals exhibited singing-related firing patterns indistinguishable from HF-2 neurons. Our data show that singing-related neural activity distinguishes two putative pallidal cell types in area X: thalamus-projecting neurons that exhibit activity similar to the primate GPi, and non-thalamus-projecting neurons that exhibit activity similar to the primate GPe. These results suggest that song learning in birds and motor learning in mammals use conserved basal ganglia signaling strategies.

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Year:  2010        PMID: 20484651      PMCID: PMC2874984          DOI: 10.1523/JNEUROSCI.0168-10.2010

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  28 in total

1.  Singing-related neural activity in a dorsal forebrain-basal ganglia circuit of adult zebra finches.

Authors:  N A Hessler; A J Doupe
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Excitatory cortical inputs to pallidal neurons via the subthalamic nucleus in the monkey.

Authors:  A Nambu; H Tokuno; I Hamada; H Kita; M Imanishi; T Akazawa; Y Ikeuchi; N Hasegawa
Journal:  J Neurophysiol       Date:  2000-07       Impact factor: 2.714

Review 3.  Evolution of the basal ganglia: new perspectives through a comparative approach.

Authors:  W J Smeets; O Marín; A González
Journal:  J Anat       Date:  2000-05       Impact factor: 2.610

4.  Miniature motorized microdrive and commutator system for chronic neural recording in small animals.

Authors:  M S Fee; A Leonardo
Journal:  J Neurosci Methods       Date:  2001-12-15       Impact factor: 2.390

5.  A telencephalic nucleus essential for song learning contains neurons with physiological characteristics of both striatum and globus pallidus.

Authors:  Michael A Farries; David J Perkel
Journal:  J Neurosci       Date:  2002-05-01       Impact factor: 6.167

6.  Identification of the anterior nucleus of the ansa lenticularis in birds as the homolog of the mammalian subthalamic nucleus.

Authors:  Y Jiao; L Medina; C L Veenman; C Toledo; L Puelles; A Reiner
Journal:  J Neurosci       Date:  2000-09-15       Impact factor: 6.167

7.  Functional correlations between neighboring neurons in the primate globus pallidus are weak or nonexistent.

Authors:  Izhar Bar-Gad; Gali Heimer; Ya'acov Ritov; Hagai Bergman
Journal:  J Neurosci       Date:  2003-05-15       Impact factor: 6.167

8.  An ultra-sparse code underlies the generation of neural sequences in a songbird.

Authors:  Richard H R Hahnloser; Alexay A Kozhevnikov; Michale S Fee
Journal:  Nature       Date:  2002-09-05       Impact factor: 49.962

9.  Independent coding of movement direction and reward prediction by single pallidal neurons.

Authors:  David Arkadir; Genela Morris; Eilon Vaadia; Hagai Bergman
Journal:  J Neurosci       Date:  2004-11-10       Impact factor: 6.167

10.  Contributions of an avian basal ganglia-forebrain circuit to real-time modulation of song.

Authors:  Mimi H Kao; Allison J Doupe; Michael S Brainard
Journal:  Nature       Date:  2005-02-10       Impact factor: 69.504

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  36 in total

1.  Integration of cortical and pallidal inputs in the basal ganglia-recipient thalamus of singing birds.

Authors:  Jesse H Goldberg; Michael A Farries; Michale S Fee
Journal:  J Neurophysiol       Date:  2012-06-06       Impact factor: 2.714

Review 2.  The avian subpallium: new insights into structural and functional subdivisions occupying the lateral subpallial wall and their embryological origins.

Authors:  Wayne J Kuenzel; Loreta Medina; Andras Csillag; David J Perkel; Anton Reiner
Journal:  Brain Res       Date:  2011-09-24       Impact factor: 3.252

Review 3.  A hypothesis for basal ganglia-dependent reinforcement learning in the songbird.

Authors:  M S Fee; J H Goldberg
Journal:  Neuroscience       Date:  2011-10-13       Impact factor: 3.590

4.  Singing-related neural activity distinguishes four classes of putative striatal neurons in the songbird basal ganglia.

Authors:  Jesse H Goldberg; Michale S Fee
Journal:  J Neurophysiol       Date:  2010-01-27       Impact factor: 2.714

Review 5.  Two tales of how expectation of reward modulates behavior.

Authors:  Long Ding; David J Perkel
Journal:  Curr Opin Neurobiol       Date:  2014-07-23       Impact factor: 6.627

6.  Vocal babbling in songbirds requires the basal ganglia-recipient motor thalamus but not the basal ganglia.

Authors:  Jesse H Goldberg; Michale S Fee
Journal:  J Neurophysiol       Date:  2011-03-23       Impact factor: 2.714

7.  Origins of basal ganglia output signals in singing juvenile birds.

Authors:  Morgane Pidoux; Tejapratap Bollu; Tori Riccelli; Jesse H Goldberg
Journal:  J Neurophysiol       Date:  2014-11-12       Impact factor: 2.714

8.  Dopaminergic modulation of basal ganglia output through coupled excitation-inhibition.

Authors:  Agata Budzillo; Alison Duffy; Kimberly E Miller; Adrienne L Fairhall; David J Perkel
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-15       Impact factor: 11.205

9.  Focal expression of mutant huntingtin in the songbird basal ganglia disrupts cortico-basal ganglia networks and vocal sequences.

Authors:  Masashi Tanaka; Jonnathan Singh Alvarado; Malavika Murugan; Richard Mooney
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-07       Impact factor: 11.205

10.  Dopamine neurons encode performance error in singing birds.

Authors:  Vikram Gadagkar; Pavel A Puzerey; Ruidong Chen; Eliza Baird-Daniel; Alexander R Farhang; Jesse H Goldberg
Journal:  Science       Date:  2016-12-08       Impact factor: 47.728

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