Changing views of basal ganglia circuits and circuit disorders
Open accessAbstract
The basal ganglia (BG) have long been considered to play an important role in the control of movement and the pathophysiology of movement disorders, such as Parkinson's disease (PD). Studies over the past decades have considerably broadened this view, indicating that the BG participate in multiple, parallel, largely segregated, cortico-subcortical reentrant pathways involving motor, associative and limbic functions. Research has shown that dysfunction within individual circuits is associated not only with movement disorders, but also with neuropsychiatric disorders. Accordingly, a number of movement disorders and neuropsychiatric disorders such as obsessive compulsive disorder and Tourette's syndrome are viewed as "circuit disorders." We here discuss the changes in our current understanding of the anatomic and functional organization of BG circuits and related circuit disorders.
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Accumulating evidence suggests neuroplasticity within the corticostriatal circuit is impaired under conditions of dopamine denervation.
“However, accumulating evidence suggest that neuroplasticity within this corticostriatal circuit is also impaired under conditions of DA denervation 41–44”
From Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease (2013) · cites this paper as [43]
Exercise can alter the storage and release of glutamate in presynaptic terminals that may improve circuit function and diminish the increased inhibitory drive of the dopamine depleted striatum.
“In addition to its receptors, exercise can also alter the storage and release of glutamate in presynaptic terminals that may also improve circuit function and diminish the increased inhibitory drive of the DA depleted striatum 41–44.”
From Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease (2013) · cites this paper as [43]
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Cites
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527 · see citing works
Self-citationThe functional anatomy of basal ganglia disorders
Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353 · see citing works
Primate models of movement disorders of basal ganglia origin
DeLong, M. R. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90110-v · Cited by 3,824 · see citing works
Self-citationTHE BASAL GANGLIA: FOCUSED SELECTION AND INHIBITION OF COMPETING MOTOR PROGRAMS
Mink, J. W. (1996) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00042-1 · Cited by 2,478 · see citing works
Alexander, G. E., Crutcher, M. D., & DeLong, M. R. (1990) · PubMed · Cited by 2,422 · see citing works
Self-citationReversal of experimental parkinsonism by lesions of the subthalamic nucleus.
Bergman, H., Wichmann, T., & Delong, M. (1990) · Science · doi:10.1126/science.2402638 · Cited by 2,003 · see citing works
Self-citation(1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62678-3 · Cited by 1,961 · see citing works
Habits, Rituals, and the Evaluative Brain
Graybiel, A. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112851 · Cited by 1,697 · see citing works
Aron, A. R., & Poldrack, R. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4682-05.2006 · Cited by 1,630 · see citing works
Pathological synchronization in Parkinson's disease: networks, models and treatments
Hammond, C., Bergman, H., & Brown, P. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.05.004 · Cited by 1,619 · see citing works
Haber, S. N., Fudge, J. L., & McFarland, N. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02369.2000 · Cited by 1,610 · see citing works
The primate basal ganglia: Parallel and integrative networks
Haber, S. N. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.10.003 · Cited by 1,479 · see citing works
Functional significance of the cortico-subthalamo-pallidal “hyperdirect” pathway
Nambu, A., Tokuno, H., & Takada, M. (2002) · Neuroscience Research · doi:10.1016/s0168-0102(02)00027-5 · Cited by 1,371 · see citing works
The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism
Bergman, H., Wichmann, T., Karmon, B., & DeLong, M. R. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.2.507 · Cited by 1,366 · see citing works
Self-citationParent, A., & Hazrati, L. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00008-d · Cited by 1,351 · see citing works
Surmeier, D. J., Ding, J., Day, M., Wang, Z., & Shen, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.008 · Cited by 1,203 · see citing works
Dichotomous dopaminergic control of striatal synaptic plasticity
Shen, W., Flajolet, M., Greengard, P., & Surmeier, D. J. (2008) · Science · doi:10.1126/science.1160575 · Cited by 1,190 · see citing works
The cerebellum communicates with the basal ganglia
Hoshi, E., Tremblay, L., Féger, J., Carras, P. L., & Strick, P. L. (2005) · Nature Neuroscience · doi:10.1038/nn1544 · Cited by 833 · see citing works
Dynamic reorganization of striatal circuits during the acquisition and consolidation of a skill
Yin, H. H., Mulcare, S. P., Hilário, M. R. F., Clouse, E., Holloway, T., Davis, M. I., Hansson, A. C., Lovinger, D. M., & Costa, R. M. (2009) · Nature Neuroscience · doi:10.1038/nn.2261 · Cited by 818 · see citing works
Functional organization of the basal ganglia: Therapeutic implications for Parkinson's disease
Obeso, J. A., Rodríguez-Oroz, M. C., Benítez‐Temiño, B., Blesa, F. J., Guridi, J., Marı́n, C., & Rodrı́guez, M. (2008) · Movement Disorders · doi:10.1002/mds.22062 · Cited by 669 · see citing works
The basal ganglia: learning new tricks and loving it
Graybiel, A. M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.10.006 · Cited by 650 · see citing works
Abnormal spontaneous activity of globus pallidus neurons in monkeys with MPTP-induced parkinsonism
Filion, M., & Tremblay, L. (1991) · Brain Research · doi:10.1016/0006-8993(91)90585-j · Cited by 641 · see citing works
The thalamostriatal system: a highly specific network of the basal ganglia circuitry
Smith, Y., Raju, D. V., Paré, J., & Sidibé, M. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.07.004 · Cited by 595 · see citing works
Pathophysiology of Parkinsonism
Galván, A., & Wichmann, T. (2008) · Clinical Neurophysiology · doi:10.1016/j.clinph.2008.03.017 · Cited by 551 · see citing works
Self-citationAziz, T. Z., Peggs, D., Sambrook, M. A., & Crossman, A. R. (1991) · Movement Disorders · doi:10.1002/mds.870060404 · Cited by 537 · see citing works
Dichotomous Anatomical Properties of Adult Striatal Medium Spiny Neurons
Gertler, T. S., Chan, C. S., & Surmeier, D. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2660-08.2008 · Cited by 469 · see citing works
Hoover, J. E., & Strick, P. L. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-04-01446.1999 · Cited by 469 · see citing works
Mallet, N. P., Pogosyan, A. H., Sharott, A., Csicsvari, J., Bolam, J. P., Brown, P., & Magill, P. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0123-08.2008 · Cited by 459 · see citing works
Akkal, D., Dum, R. P., & Strick, P. L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3134-07.2007 · Cited by 437 · see citing works
Joel, D., & Weiner, I. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90536-3 · Cited by 430 · see citing works
Miller, W. C., & DeLong, M. R. (1987) · Advances in behavioral biology · doi:10.1007/978-1-4684-5347-8_29 · Cited by 427 · see citing works
Self-citationThe connexions of the striatum and globus pallidus: synthesis and speculation
Kemp, J. M., & Powell, T. P. S. (1971) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1971.0106 · Cited by 385 · see citing works
The primate subthalamic nucleus. I. Functional properties in intact animals
Wichmann, T., Bergman, H., & DeLong, M. R. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.2.494 · Cited by 372 · see citing works
Self-citationGeorgopoulos, A. P., DeLong, M., & Crutcher, M. D. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-08-01586.1983 · Cited by 363 · see citing works
Self-citationPedunculopontine nucleus and basal ganglia: distant relatives or part of the same family?
Mena‐Segovia, J., Bolam, J. P., & Magill, P. J. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.07.009 · Cited by 349 · see citing works
Deep Brain Stimulation for Neurologic and Neuropsychiatric Disorders
Wichmann, T., & DeLong, M. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.022 · Cited by 331 · see citing works
Self-citationThe basal ganglia and cerebellum interact in the expression of dystonic movement
Neychev, V. K., Fan, X., Mitev, V., Hess, E. J., & Jinnah, H. A. (2008) · Brain · doi:10.1093/brain/awn168 · Cited by 316 · see citing works
Organization of the basal ganglia: the importance of axonal collateralization
Parent, A., Sato, F., Wu, Y. N., Gauthier, J., Lévesque, M., & Parent, M. (2000) · Trends in Neurosciences · doi:10.1016/s1471-1931(00)00022-7 · Cited by 306 · see citing works
Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia
Árgyelán, M., Carbon, M., Niethammer, M., Uluğ, A. M., Voss, H. U., Bressman, S., DHAWAN, V. M., & Eidelberg, D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2300-09.2009 · Cited by 304 · see citing works
Shink, É., Bevan, M. D., Bolam, J. P., & Smith, Y. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00022-x · Cited by 296 · see citing works
Long-term follow-up of unilateral pallidotomy in advanced Parkinson's disease.
Fine, J., Duff, J., Chen, R., Chir, B., Hutchison, W., Lozano, A., & Lang, A. (2000) · New England Journal of Medicine · doi:10.1056/nejm200006083422304 · Cited by 279 · see citing works
Neural mechanisms in disorders of movement
Crossman, A. R. (1989) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(89)90201-6 · Cited by 276 · see citing works
François, C. (2004) · Brain · doi:10.1093/brain/awh239 · Cited by 275 · see citing works
Joel, D., & Weiner, I. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00018-5 · Cited by 269 · see citing works
A new dynamic model of the cortico-basal ganglia loop
Nambu, A. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)43043-4 · Cited by 263 · see citing works
Pallidal Discharge Related to the Kinematics of Reaching Movements in Two Dimensions
Turner, R. S., & Anderson, M. E. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.3.1051 · Cited by 246 · see citing works
Differential Excitability and Modulation of Striatal Medium Spiny Neuron Dendrites
Day, M., Wokosin, D. L., Plotkin, J. L., Tian, X., & Surmeier, D. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1840-08.2008 · Cited by 242 · see citing works
Basal Ganglia and Cerebellar Inputs to ‘AIP’
Clower, D. M., Dum, R. P., & Strick, P. L. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh190 · Cited by 242 · see citing works
Grabli, D. (2004) · Brain · doi:10.1093/brain/awh220 · Cited by 241 · see citing works
Update on models of basal ganglia function and dysfunction
DeLong, M. R., & Wichmann, T. (2009) · Parkinsonism & Related Disorders · doi:10.1016/s1353-8020(09)70822-3 · Cited by 231 · see citing works
Self-citationKelly, R. M., & Strick, P. L. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)43042-2 · Cited by 228 · see citing works
Bilateral subthalamotomy in Parkinson's disease: initial and long-term response.
Alvarez, L., Macias, R., López, G., Alvarez, E., Pavón, N., Rodríguez-Oroz, M., Juncos, J., Maragoto, C., Guridi, J., Litvan, I., et al. (2005) · Brain : a journal of neurology · doi:10.1093/brain/awh397 · Cited by 221 · see citing works
Self-citationThe primate globus pallidus: neuronal activity related to direction of movement
Mitchell, S. J., Richardson, R. T., Baker, F., & DeLong, M. R. (1987) · Experimental Brain Research · doi:10.1007/bf00249793 · Cited by 175 · see citing works
Self-citationFilion, M. (1979) · Brain Research · doi:10.1016/0006-8993(79)90704-2 · Cited by 168 · see citing works
Romanelli, P., Esposito, V., Schaal, D. W., & Heit, G. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.09.008 · Cited by 163 · see citing works
Late emergence of synchronized oscillatory activity in the pallidum during progressive parkinsonism
Leblois, A., Meissner, W. G., Bioulac, B. H., Gross, C. E., Hansel, D., & Boraud, T. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05777.x · Cited by 160 · see citing works
Corticostriatal Activity in Primary Motor Cortex of the Macaque
Turner, R. S., & DeLong, M. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-07096.2000 · Cited by 159 · see citing works
Self-citationThe neurophysiological correlates of motor tics following focal striatal disinhibition
McCairn, K. W., Bronfeld, M., Belelovsky, K., & Bar‐Gad, I. (2009) · Brain · doi:10.1093/brain/awp142 · Cited by 151 · see citing works
Alexander, G. E., & DeLong, M. R. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.53.6.1401 · Cited by 143 · see citing works
Self-citationA new twist on the anatomy of dystonia
Jinnah, H. A., & Hess, E. J. (2006) · Neurology · doi:10.1212/01.wnl.0000246112.19504.61 · Cited by 139 · see citing works
Hamada, I., & DeLong, M. R. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.68.5.1859 · Cited by 128 · see citing works
Self-citation(1987) · Advances in behavioral biology · doi:10.1007/978-1-4684-5347-8 · Cited by 127 · see citing works
Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study
Carbon, M., Ghilardi, M. F., Árgyelán, M., DHAWAN, V. M., Bressman, S., & Eidelberg, D. (2007) · Brain · doi:10.1093/brain/awm243 · Cited by 111 · see citing works
Obeso, J. A., Jahanshahi, M., Álvarez, L., Macıás, R., Pedroso, I., Wilkinson, L., Pavon, N., Day, B. L., Pinto, S., Rodríguez‐Oroz, M., et al. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.08.030 · Cited by 109 · see citing works
Motor learning in monkeys (Macaca fascicularis) with lesions in motor thalamus
Canavan, A. G. M., Nixon, P. D., & Passingham, R. E. (1989) · Experimental Brain Research · doi:10.1007/bf00250573 · Cited by 102 · see citing works
Bauswein, E., Fromm, C., & Preuss, A. (1989) · Brain Research · doi:10.1016/0006-8993(89)91018-4 · Cited by 96 · see citing works
Functional anatomy of movement disorders
Crossman, A. R. (2000) · Journal of Anatomy · doi:10.1046/j.1469-7580.2000.19640519.x · Cited by 94 · see citing works
Rossi, L., Marceglia, S. R. F., Foffani, G., Cogiamanian, F. M., Tamma, F., Rampini, P. M., Barbieri, S., Bracchi, F., & Priori, A. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.01.023 · Cited by 91 · see citing works
A new approach to understand the pathophysiology of Parkinson’s disease
Nambu, A. (2005) · Journal of Neurology · doi:10.1007/s00415-005-4002-y · Cited by 85 · see citing works
Kliem, M. A., Maidment, N. T., Ackerson, L. C., Chen, S., Smith, Y., & Wichmann, T. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00171.2007 · Cited by 75 · see citing works
Self-citationAnatomy and physiology of the basal ganglia: relevance to Parkinson's disease and related disorders
Wichmann, T., & DeLong, M. R. (2007) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)83001-6 · Cited by 61 · see citing works
Self-citationBasal ganglia contribution to the initiation of corrective submovements
Tunik, E., Houk, J. C., & Grafton, S. T. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.077 · Cited by 54 · see citing works
A quantitative analysis of pallidal discharge during targeted reaching movement in the monkey
Anderson, M. E., & Turner, R. S. (1991) · Experimental Brain Research · doi:10.1007/bf00230536 · Cited by 48 · see citing works
Effects of Striatal GABAA-Receptor Blockade on Striatal and Cortical Activity in Monkeys
Darbin, O., & Wichmann, T. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01191.2007 · Cited by 33 · see citing works
Self-citationRestivo, L. (2010) · Frontiers in Integrative Neuroscience · doi:10.3389/neuro.07.001.2010 · Cited by 32 · see citing works
Brain mechanisms for switching from automatic to controlled eye movements
Hikosaka, O., & Isoda, M. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00655-9 · Cited by 26 · see citing works
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Redgrave, P., Rodriguez, M., Smith, Y., Rodriguez-Oroz, M. C., Lehericy, S., Bergman, H., Agid, Y., DeLong, M. R., & Obeso, J. A. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2915 · Cited by 1,134 · see citing works
The basal ganglia and the cerebellum: nodes in an integrated network
Bostan, A. C., & Strick, P. L. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0002-7 · Cited by 786 · see citing works
Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease
Petzinger, G. M., Fisher, B. E., McEwen, S., Beeler, J. A., Walsh, J. P., & Jakowec, M. W. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70123-6 · Cited by 798 · see citing works
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Hernandez, L. M., Lawrence, K. E., Padgaonkar, N. T., Inada, M., Hoekstra, J. N., Lowe, J. K., Eilbott, J., Jack, A., Aylward, E., Gaab, N., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0750-9 · Cited by 54 · see citing works
Heinzel, S., Kaufmann, C., Grützmann, R., Klawohn, J., Riesel, A., Bey, K., Heilmann-Heimbach, S., Weinhold, L., Ramirez, A., Wagner, M., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-98333-w · Cited by 23 · see citing works
- Authors
- DeLong, M., & Wichmann, T.
- Affiliations
- Emory University (US)
- Corresponding author
- DeLong, Mahlon
- Venue
- Clinical EEG and Neuroscience
- Publisher
- SAGE Publications
- Published
- 2010-04
- Volume
- 41
- Issue
- 2
- Pages
- 61-67
- ISSN
- 1550-0594 (ISSN-L)
- 2169-5202
- PMC
- PMC4305332
- OpenAlex
- W2139464784
- Cited by
- 128
- References
- 76
- Citations by year
- 2026: 3 · 2025: 11 · 2024: 5 · 2023: 4 · 2022: 13 · 2021: 9 · 2020: 17 · 2019: 11 · 2018: 10 · 2017: 9 · 2016: 12 · 2015: 6 · 2014: 3 · 2013: 4 · 2012: 4
- FWCI
- 2.86
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Clinical EEG and Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS054976, P50NS071669)
- National Center for Research Resources (P51RR000165)
- Topics
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Social Sciences › Psychology › Clinical Psychology › Obsessive-Compulsive Spectrum Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- basal ganglia, basal ganglia circuitry, movement disorders, Parkinson's disease, neuropsychiatric disorders, obsessive-compulsive disorder, Tourette syndrome, associative functions
- MeSH terms
- Basal Ganglia, Basal Ganglia Diseases, Humans, Models, Neurological, Nerve Net, Parkinson Disease
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