Mean-field modeling of the basal ganglia-thalamocortical system. I. Firing rates in healthy and parkinsonian states

Journal of Theoretical Biology

Volumn 257, Issue 4, 2009, Pages 642-663

  van Albada, S J ^a,b   Robinson, P A ^a,b,c  

^a UNIVERSITY OF SYDNEY   (Australia)

^b WESTMEAD HOSPITAL   (Australia)

^c University of Sydney   (Australia)

Author keywords

Direct pathway; Dopamine loss; Indirect pathway; Mathematical model; Nigrostriatal degeneration; Parkinson's disease

Indexed keywords

DOPAMINE;

CYTOLOGY; MODELING; NERVOUS SYSTEM; NERVOUS SYSTEM DISORDER; PHYSIOLOGICAL RESPONSE;

ARTICLE; BASAL GANGLION; BRAIN ELECTROPHYSIOLOGY; CATECHOLAMINE DEPLETION; GLOBUS PALLIDUS; MATHEMATICAL MODEL; NERVE CELL EXCITABILITY; NERVE PROJECTION; PARKINSONISM; PRIORITY JOURNAL; STRIATONIGRAL DEGENERATION; SUBTHALAMIC NUCLEUS; THALAMOCORTICAL TRACT;

ADULT; ANIMALS; BASAL GANGLIA; CEREBRAL CORTEX; HUMANS; MODELS, NEUROLOGICAL; NEURAL INHIBITION; NEURAL PATHWAYS; PARKINSONIAN DISORDERS; SUBTHALAMIC NUCLEUS; THALAMUS;

PARKINSONIA;

EID: 62749110454     PISSN: 00225193     EISSN: 10958541     Source Type: Journal    
DOI: 10.1016/j.jtbi.2008.12.018     Document Type: Article

References (271)

1. Afsharpour S. Topographical projections of the cerebral cortex to the subthalamic nucleus. J. Comp. Neurol. 236 (1985) 14-28
2. 2 dopamine receptor colocalization in neostriatal neurons. Nat. Neurosci. 3 (2000) 226-230
3. Albin R.L., Young A.B., and Penney J.B. The functional anatomy of basal ganglia disorders. Trends Neurosci. 12 (1989) 366-375
4. Alexander G.E., and Crutcher M.D. Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 13 (1990) 266-271
5. Alexander G.E., DeLong M.R., and Strick P.L. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Ann. Rev. Neurosci. 9 (1986) 357-381
6. Anaya-Martinez V., Martinez-Marcos A., Martinez-Fong D., Aceves J., and Erlij D. Substantia nigra compacta neurons that innervate the reticular thalamic nucleus in the rat also project to striatum or globus pallidus: implications for abnormal motor behavior. Neuroscience 143 (2006) 477-486
7. Anderson M.E., and Turner R.S. Activity of neurons in cerebellar-receiving and pallidal-receiving areas of the thalamus of the behaving monkey. J. Neurophysiol. 66 (1991) 879-893
8. Aosaki T., Kimura M., and Graybiel A.M. Temporal and spatial characteristics of tonically active neurons of the primate's striatum. J. Neurophysiol. 73 (1995) 1234-1252
9. Augood S.J., Emson P.C., Mitchell I.J., Boyce S., Clarke C.E., and Crossman A.R. Cellular localisation of enkephalin gene expression in MPTP-treated cynomolgus monkeys. Mol. Brain Res. 6 (1989) 85-92
10. Aziz T.Z., Davies L., and France S. The role of descending basal ganglia connections to the brain stem in Parkinsonian akinesia. Br. J. Neurosurgery 12 (1998) 245-249
11. Bar-Gad I., Morris G., and Bergman H. Information processing, dimensionality reduction and reinforcement learning in the basal ganglia. Prog. Neurobiol. 71 (2003) 439-473
12. Benazzouz A., Gao D.M., Ni Z.G., Piallat B., Bouali-Benazzouz R., and Benabid A.L. Effect of high-frequency stimulation of the subthalamic nucleus on the neuronal activities of the substantia nigra pars reticulata and ventrolateral nucleus of the thalamus in the rat. Neuroscience 99 (2000) 289-295
13. Benazzouz A., Breit S., Koudsie A., Pollak P., Krack P., and Benabid A.L. Intraoperative microrecordings of the subthalamic nucleus in Parkinson's disease. Mov. Disord. 17 Suppl. 3 (2002) S145-S149
14. Bergman H., and Deuschl G. Pathophysiology of Parkinson's disease: from clinical neurology to basic neuroscience and back. Mov. Disord. 17 Suppl. 3 (2002) S28-S40
15. Bergman H., Wichmann T., Karmon B., and DeLong M.R. The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism. J. Neurophysiol. 72 (1994) 507-520
16. Betarbet R., and Greenamyre J.T. Regulation of dopamine receptor and neuropeptide expression in the basal ganglia of monkeys treated with MPTP. Exp. Neurol. 189 (2004) 393-403
17. Blackwell K.T., Czubayko K.T., and Plenz D. Quantitative estimate of synaptic inputs to striatal neurons during up and down states in vitro. J. Neurosci. 23 (2003) 9123-9132
18. Blandini F., Nappi G., Tassorelli C., and Martignoni E. Functional changes of the basal ganglia circuitry in Parkinson's disease. Prog. Neurobiol. 62 (2000) 63-88
19. Bolam J.P., Hanley J.J., Booth P.A.C., and Bevan M.D. Synaptic organisation of the basal ganglia. J. Anat. 196 (2000) 527-542
20. Boraud T., Bezard E., Guehl D., Bioulac B., and Gross C. Effects of l-DOPA on neuronal activity of the globus pallidus externalis (GPe) and globus pallidus internalis (GPi) in the MPTP-treated monkey. Brain Res. 787 (1998) 157-160
21. Braitenberg V., and Schüz A. Cortex: Statistics and Geometry of Neuronal Connectivity. second ed. (1998), Springer, Berlin, Heidelberg, New York
22. Breakspear M., Roberts J.A., Terry J.R., Rodrigues S., Mahant N., and Robinson P.A. A unifying explanation of primary generalized seizures through nonlinear brain modeling and bifurcation analysis. Cereb. Cortex 16 (2006) 1296-1313
23. Breit S., Bouali-Benazzouz R., Benabid A.-L., and Benazzouz A. Unilateral lesion of the nigrostriatal pathway induces an increase of neuronal activity of the pedunculopontine nucleus, which is reversed by the lesion of the subthalamic nucleus in the rat. Eur. J. Neurosci. 14 (2001) 1833-1842
24. Breit S., Lessmann L., Unterbrink D., Popa R.C., Gasser T., and Schulz J.B. Lesion of the pedunculopontine nucleus reverses hyperactivity of the subthalamic nucleus and substantia nigra pars reticulata in a 6-hydroxydopamine rat model. Eur. J. Neurosci. 24 (2006) 2275-2282
25. Bressloff P.C. Traveling fronts and wave propagation failure in an inhomogeneous neural network. Physica D 155 (2001) 83-100
26. Bressloff P.C., Folias S.E., Prat A., and Li Y.-X. Oscillatory waves in inhomogeneous neural media. Phys. Rev. Lett. 91 (2003) 178101.1-178101.4
27. Brown P. Cortical drives to human muscle: the Piper and related rhythms. Prog. Neurobiol. 60 (2000) 97-108
28. Brown L.L., Makman M.H., Wolfson L.I., Dvorkin B., Warner C., and Katzman R. A direct role of dopamine in the rat subthalamic nucleus and adjacent intrapeduncular area. Science 206 (1979) 1416-1418
29. Bruno R.M., and Sakmann B. Cortex is driven by weak but synchronously active thalamocortical synapses. Science 312 (2006) 1622-1627
30. Budd J.M.L. How much feedback from visual cortex to lateral geniculate nucleus in cat: a perspective. Visual Neurosci. 21 (2004) 487-500
31. Burbaud P., Gross C., Benazzouz A., and Coussemacq M. Reduction of apomorphine-induced rotational behaviour by subthalamic lesion in 6-OHDA lesioned rats is associated with a normalization of firing rate and discharge patterns of pars reticulata neurons. Exp. Brain Res. 105 (1995) 48-58
32. Burns B.D. Some properties of isolated cerebral cortex in the unanaesthetized cat. J. Physiol. 112 (1951) 156-175
33. Calabresi P., Centonze D., Gubellini P., Marfia G.A., Pisani A., Sancesario G., and Bernardi G. Synaptic transmission in the striatum: from plasticity to neurodegeneration. Prog. Neurobiol. 61 (2000) 231-265
34. Campbell G.A., Eckardt M.J., and Weight F.F. Dopaminergic mechanisms in subthalamic nucleus of rat: analysis using horseradish peroxidase and microiontophoresis. Brain Res. 333 (1985) 261-270
35. Carpenter, M.B., 1981. Anatomy of the corpus striatum and brain stem integrating systems. In: Handbook of Physiology, vol. 2. American Physiological Society, Bethesda, MD, pp. 947-995.
36. Cepeda C., Colwell C.S., Itri J.N., Chandler S.H., and Levine M.S. Dopaminergic modulation of NMDA-induced whole cell currents in neostriatal neurons in slices: contribution of calcium conductances. J. Neurophysiol. 79 (1998) 82-94
37. Chen M.-T., Morales M., Woodward D.J., Hoffer B.J., and Janak P.H. In vivo extracellular recording of striatal neurons in the awake rat following unilateral 6-hydroxydopamine lesions. Exp. Neurol. 171 (2001) 72-83
38. Cheruel F., Dormont J.F., and Farin D. Activity of neurons of the subthalamic nucleus in relation to motor performance in the cat. Exp. Brain Res. 108 (1996) 206-220
39. Chervin R.D., Pierce P.A., and Connors B.W. Periodicity and directionality in the propagation of epileptiform discharges across neocortex. J. Neurophysiol. 60 (1988) 1695-1713
40. Clugnet M.-C., LeDoux J.E., and Morrison S.F. Unit responses evoked in the amygdala and striatum by electrical stimulation of the medial geniculate body. J. Neurosci. 10 (1990) 1055-1061
41. Cooper A.J., and Stanford I.M. Electrophysiological and morphological characteristics of three subtypes of rat globus pallidus neurone in vitro. J. Physiol. 527 (2000) 291-304
42. Cornwall J., Cooper J.D., and Phillipson O.T. Projections to the rostral reticular thalamic nucleus in the rat. Exp. Brain Res. 80 (1990) 157-171
43. Cox C.L., Huguenard J.R., and Prince D.A. Nucleus reticularis neurons mediate diverse inhibitory effects in thalamus. Proc. Natl. Acad. Sci. USA 94 (1997) 8854-8859
44. Day M., Wang Z., Ding J., An X., Ingham C.A., Shering A.F., Wokosin D., Ilijic E., Sun Z., Sampson A.R., Mugnaini E., Deutch A.Y., Sesack S.R., Arbuthnott G.W., and Surmeier D.J. Selective elimination of glutamatergic synapses on striatopallidal neurons in Parkinson disease models. Nat. Neurosci. 9 (2006) 2006
45. Dejean C., Gross C.E., Bioulac B., and Boraud T. Dynamic changes in the cortex-basal ganglia network after dopamine depletion in the rat. J. Neurophysiol. 100 (2008) 385-396
46. DeLong M.R. Activity of pallidal neurons during movement. J. Neurophysiol. 34 (1971) 414-427
47. DeLong M.R. Primate models of movement disorders of basal ganglia origin. Trends Neurosci. 13 (1990) 281-285
48. DeLong M.R., Crutcher M.D., and Georgopoulos A.P. Relations between movement and single cell discharge in the substantia nigra of the behaving monkey. J. Neurosci. 3 (1983) 1599-1606
49. DeLong M.R., Crutcher M.D., and Georgopoulos A.P. Primate globus pallidus and subthalamic nucleus: functional organization. J. Neurophysiol. 53 (1985) 530-543
50. Deng Y.P., Albin R.L., Penney J.B., Young A.B., Anderson K.D., and Reiner A. Differential loss of striatal projection systems in Huntington's disease: a quantitative immunohistochemical study. J. Chem. Neuroanat. 27 (2004) 143-164
51. Destexhe A., and Sejnowski T.J. Thalamocortical Assemblies: How Ion Channels, Single Neurons, and Large-Scale Networks Organize Sleep Oscillations (2001), Oxford University Press, Oxford
52. Destexhe A., and Sejnowski T.J. Interactions between membrane conductances underlying thalamocortical slow-wave oscillations. Physiol. Rev. 83 (2003) 1401-1453
53. 2 receptor stimulation on somatostatin, neuropeptide Y, neurotensin, dynorphin and enkephalin. Brain Res. 581 (1992) 261-268
54. Engblom A.C., Johansen F.F., and Kristiansen U. Actions and interactions of extracellular potassium and kainate on expression of 13 γ-aminobutyric acid type A receptor subunits in cultured mouse cerebellar granule neurons. J. Biol. Chem. 278 (2003) 16543-16550
55. Erişir A., Van Horn S.C., Bickford M.E., and Sherman S.M. Immunocytochemistry and distribution of parabrachial terminals in the lateral geniculate nucleus of the cat: a comparison with corticogeniculate terminals. J. Comp. Neurol. 377 (1997) 535-549
56. Filion M., and Tremblay L. Abnormal spontaneous activity of globus pallidus neurons in monkeys with MPTP-induced parkinsonism. Brain Res. 547 (1991) 142-151
57. Floran B., Floran L., Sierra A., and Aceves J. D2 receptor-mediated inhibition of GABA release by endogenous dopamine in the rat globus pallidus. Neurosci. Lett. 237 (1997) 1-4
58. Flores G., Liang J.J., Martinez-Fong D., Quirion R., Aceves J., and Srivastava L.K. Expression of dopamine receptors in the subthalamic nucleus of the rat: characterization using reverse transcriptase polymerase chain reaction and autoradiography. Neuroscience 91 (1999) 549-556
59. Fujikawa D.G., Kim J.S., Daniels A.H., Alcaraz A.F., and Sohn T.B. In vivo elevation of extracellular potassium in the rat amygdala increases extracellular glutamate and aspartate and damages neurons. Neuroscience 74 (1996) 695-706
60. Gandia J.A., De Las Heras S., García M., and Giménez-Amaya J.M. Afferent projections to the reticular thalamic nucleus from the globus pallidus and the substantia nigra in the rat. Brain Res. Bull. 32 (1993) 351-358
61. Gao W.-J., and Goldman-Rakic P.S. Selective modulation of excitatory and inhibitory microcircuits by dopamine. Proc. Natl. Acad. Sci. USA 100 (2003) 2836-2841
62. Gaspar P., Stepniewska I., and Kaas J.H. Topography and collateralization of the dopaminergic projections to motor and lateral prefrontal cortex in owl monkeys. J. Comp. Neurol. 325 (1992) 1-21
63. Gentet L.J., and Ulrich D. Strong, reliable and precise synaptic connections between thalamic relay cells and neurones of the nucleus reticularis in juvenile rats. J. Physiol. 546 (2003) 801-811
64. Georgopoulos A.P., DeLong M.R., and Crutcher M.D. Relations between parameters of step-tracking movements and single cell discharge in the globus pallidus and subthalamic nucleus of the behaving monkey. J. Neurosci. 3 (1983) 1586-1598
65. Gerfen C.R., Herkenham M., and Thibault J. The neostriatal mosaic: II. Patch- and matrix-directed mesostriatal dopaminergic and non-dopaminergic systems. J. Neurosci. 7 (1987) 3915-3934
66. Gerfen C.R., Engber T.M., Mahan L.C., Susel Z., Chase T.N., Monsma Jr. F.J., and Sibley D.R. D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. Science 250 (1990) 1429-1432
67. Gerfen C.R. The neostriatal mosaic: multiple levels of compartmental organization. Trends Neurosci. 15 (1992) 133-139
68. Gil Z., Connors B.W., and Amitai Y. Efficacy of thalamocortical and intracortical synaptic connections: quanta, innervation, and reliability. Neuron 23 (1999) 385-397
69. 14C]-2-deoxyglucose uptake in the MPTP-treated marmoset: relationship to locomotor activity. J. Neural Transm. 101 (1995) 65-82
70. Goldberg J.A., Boraud T., Maraton S., Haber S.N., Vaadia E., and Bergman H. Enhanced synchrony among primary motor cortex neurons in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine primate model of Parkinson's disease. J. Neurosci. 22 (2002) 4639-4653
71. Goldman-Rakic P.S., and Selemon L.D. New frontiers in basal ganglia research. Trends Neurosci. 13 (1990) 241-244
72. Golomb D., and Amitai Y. Propagating neuronal discharges in neocortical slices: computational and experimental study. J. Neurophysiol. 78 (1997) 1199-1211
73. Golshani P., Liu X.-B., and Jones E.G. Differences in quantal amplitude reflect GluR4-subunit number at corticothalamic synapses on two populations of thalamic neurons. Proc. Natl. Acad. Sci. 98 (2001) 4172-4177
74. Gonzalo N., Lanciego J.L., Castle M., Vázquez A., Erro E., and Obeso J.A. The parafascicular thalamic complex and basal ganglia circuitry: further complexity to the basal ganglia model. Thal. Rel. Syst. 1 (2002) 341-348
75. Granseth B., and Lindström S. Unitary EPSCs of corticogeniculate fibers in the rat dorsal lateral geniculate nucleus in vitro. J. Neurophysiol. 89 (2003) 2952-2960
76. Gray J.A., Feldon J., and Rawlins J.N.P. The neuropsychology of schizophrenia. Behav. Brain Sci. 14 (1991) 1-19
77. Graybiel A.M. Neurotransmitters and neuromodulators in the basal ganglia. Trends Neurosci. 13 (1990) 244-254
78. Groves P.M., Garcia-Munoz M., Linder J.C., Manley M.S., Martone M.E., and Young S.J. Elements of the intrinsic organization and information processing in the neostriatum. In: Houk J., Davis J., and Beiser D. (Eds). Models of Information Processing in the Basal Ganglia (1995), MIT Press, Cambridge, MA 51-96
79. Gulledge A.T., and Jaffe D.B. Multiple effects of dopamine on layer V pyramidal cell excitability in rat prefrontal cortex. J. Neurophysiol. 86 (2001) 586-595
80. Gurney K., Prescott T.J., and Redgrave P. A computational model of action selection in the basal ganglia. I. A new functional anatomy. Biol. Cybern. 84 (2001) 401-410
81. Gurney K., Prescott T.J., and Redgrave P. A computational model of action selection in the basal ganglia. II. Analysis and simulation of behaviour. Biol. Cybern. 84 (2001) 411-423
82. Haber S.N., and Gdowski M.J. The basal ganglia. In: Paxinos G., and Mai J. (Eds). The Human Nervous System (2004), Elsevier, Amsterdam 676-738
83. Haber S.N., Fudge J.L., and McFarland N.R. Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum. J. Neurosci. 20 (2000) 2369-2382
84. Hamada I., and DeLong M.R. Excitotoxic acid lesions of the primate subthalamic nucleus result in reduced pallidal neuronal activity during active holding. J. Neurophysiol. 68 (1992) 1859-1866
85. Hanley J.J., and Bolam J.P. Synaptology of the nigrostriatal projection in relation to the compartmental organization of the neostriatum in the rat. Neuroscience 81 (1997) 353-370
86. Hashimoto T., Elder C.M., Okun M.S., Patrick S.K., and Vitek J.L. Stimulation of the subthalamic nucleus changes the firing pattern of pallidal neurons. J. Neurosci. 23 (2003) 1916-1923
87. Hassani O.-K., Mouroux M., and Féger J. Increased subthalamic neuronal activity after nigral dopaminergic lesion independent of disinhibition via the globus pallidus. Neuroscience 72 (1996) 105-115
88. Hassani O.-K., François C., Yelnik J., and Féger J. Evidence for a dopaminergic innervation of the subthalamic nucleus in the rat. Brain Res. 749 (1997) 88-94
89. Hazrati L.-N., and Parent A. Projection from the external pallidum to the reticular thalamic nucleus in the squirrel monkey. Brain Res. 550 (1991) 142-146
90. Hazrati L.-N., Parent A., Mitchell S., and Haber S.N. Evidence for interconnections between the two segments of the globus pallidus in primates: a PHA-L anterograde tracing study. Brain Res. 533 (1990) 171-175
91. Heimer G., Bar-Gad I., Goldberg J.A., and Bergman H. Dopamine replacement therapy reverses abnormal synchronization of pallidal neurons in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine primate model of Parkinsonism. J. Neurosci. 22 (2002) 7850-7855
92. 2 + conductance. J. Neurosci. 17 (1997) 3334-3342
93. Hersch S.M., Ciliax B.J., Gutekunst C.-A., Rees H.D., Heilman C.J., Yung K.K.L., Bolam J.P., Ince E., Yi H., and Levey A.I. Electron microscopic analysis of D1 and D2 dopamine receptor proteins in the dorsal striatum and their synaptic relationships with motor corticostriatal afferents. J. Neurosci. 15 (1995) 5222-5237
94. Hestrin S., Sah P., and Nicoll R.A. Mechanisms generating the time course of dual component excitatory synaptic currents recorded in hippocampal slices. Neuron 5 (1990) 247-253
95. Hollerman J.R., and Grace A.A. Subthalamic nucleus cell firing in the 6-OHDA-treated rat: basal activity and response to haloperidol. Brain Res. 590 (1992) 291-299
96. 2 dopaminergic receptors mediate inhibition of excitatory synaptic transmission in rat neostriatum. Brain Res. 690 (1995) 264-268
97. 1 receptor stimulation. J. Neurosci. 10 (1990) 2318-2329
98. 2 class receptors. Neurosci. Lett. 224 (1997) 61-65
99. Humphries M.D., and Gurney K.N. A pulsed neural network model of bursting in the basal ganglia. Neural Networks 14 (2001) 845-863
100. Humphries M.D., Stewart R.D., and Gurney K.N. A physiologically plausible model of action selection and oscillatory activity in the basal ganglia. J. Neurosci. 26 (2006) 12921-12942
101. Hutchison W.D., Lozano A.M., Davis K.D., Saint-Cyr J.A., Lang A.E., and Dostrovsky J.O. Differential neuronal activity in segments of globus pallidus in Parkinson's disease patients. NeuroReport 5 (1994) 1533-1537
102. Hutchison W.D., Allan R.J., Opitz H., Levy R., Dostrovsky J.O., Lang A.E., and Lozano A.M. Neurophysiological identification of the subthalamic nucleus in surgery for Parkinson's disease. Ann. Neurol. 44 (1998) 622-628
103. Ilinsky I.A., Tourtellotte W.G., and Kultas-Ilinsky K. Anatomical distinctions between the two basal ganglia afferent territories in the primate motor thalamus. Stereotact. Funct. Neurosurg. 60 (1993) 62-69
104. Inase M., Li B.-M., and Tanji J. Dopaminergic modulation of neuronal activity in the monkey putamen through D1 and D2 receptors during a delayed Go/Nogo task. Exp. Brain Res. 117 (1997) 207-218
105. Jackson S.R., Marrocco R., and Posner M.I. Networks of anatomical areas controlling visuospatial attention. Neural Networks 7 (1994) 925-944
106. Jan C., Franç0ois C., Tandé D., Yelnik J., Tremblay L., Agid Y., and Hirsch E. Dopaminergic innervation of the pallidum in the normal state, in MPTP-treated monkeys and in parkinsonian patients. Eur. J. Neurosci. 12 (2000) 4525-4535
107. Jenkins I.H., Fernandez W., Playford E.D., Lees A.J., Frackowiak R.S.J., Passingham R.E., and Brooks D.J. Impaired activation of the supplementary motor area in Parkinson's disease is reversed when akinesia is treated with apomorphine. Ann. Neurol. 32 (1992) 749-757
108. Jiménez-Castellanos J., and Graybiel A.M. Compartmental origins of striatal efferent projections in the cat. Neuroscience 32 (1989) 297-321
109. Jirsa V.K., and Haken H. Field theory of electromagnetic brain activity. Phys. Rev. Lett. 77 (1996) 960-963
110. Jirsa V.K., and Haken H. A derivation of a macroscopic field theory of the brain from the quasi-microscopic neural dynamics. Physica D 99 (1997) 503-526
111. Joyce J.N., Lexow N., Bird E., and Winokur A. Organization of dopamine D1 and D2 receptors in human striatum: receptor autoradiographic studies in Huntington's disease and schizophrenia. Synapse 2 (1988) 546-557
112. Kawaguchi Y., Wilson C.J., Augood S.J., and Emson P.C. Striatal interneurons: chemical, physiological and morphological characterization. Trends Neurosci. 18 (1995) 527-535
113. Kerr C.C., Rennie C.J., and Robinson P.A. Physiology-based modeling of cortical auditory evoked potentials. Biol. Cybern. 98 (2008) 171-184
114. Kim R., Nakano K., Jayaraman A., and Carpenter M.B. Projections of the globus pallidus and adjacent structures: an autoradiographic study in the monkey. J. Comp. Neurol. 169 (1976) 263-290
115. Kimura M., Rajkowski J., and Evarts E. Tonically discharging putamen neurons exhibit set-dependent responses. Proc. Natl. Acad. Sci. USA 81 (1984) 4998-5001
116. Kimura M., Kato M., Shimazaki H., Watanabe K., and Matsumoto N. Neural information transferred from the putamen to the globus pallidus during learned movement in the monkey. J. Neurophysiol. 76 (1996) 3771-3786
117. Kish L.J., Palmer M.R., and Gerhardt G.A. Multiple single-unit recordings in the striatum of freely moving animals: effects of apomorphine and D-amphetamine in normal and unilateral 6-hydroxydopamine-lesioned rats. Brain Res. 833 (1999) 58-70
118. Kita H. Parvalbumin-immunopositive neurons in rat globus pallidus: a light and electron microscopic study. Brain Res. 657 (1994) 31-41
119. Kita H. Neostriatal and globus pallidus stimulation induced inhibitory postsynaptic potentials in entopeduncular neurons in rat brain slice preparations. Neuroscience 105 (2001) 871-879
120. Kita H., Chang H., and Kitai S. Pallidal inputs to subthalamus: intracellular analysis. Brain Res. 264 (1983) 255-265
121. Kita H., Tokuno H., and Nambu A. Monkey globus pallidus external segment neurons projecting to the neostriatum. NeuroReport 10 (1999) 1467-1472
122. Kita H., Nambu A., Kaneda K., Tachibana Y., and Takada M. Role of ionotropic glutamatergic and GABAergic inputs on the firing activity of neurons in the external pallidum in awake monkeys. J. Neurophysiol. 92 (2004) 3069-3084
123. Kiyatkin E.A., and Rebec G.V. Dopaminergic modulation of glutamate-induced excitations of neurons in the neostriatum and nucleus accumbens of awake, unrestrained rats. J. Neurophysiol. 75 (1996) 142-153
124. Kiyatkin E.A., and Rebec G.V. Striatal neuronal activity and responsiveness to dopamine and glutamate after selective blockade of D1 and D2 dopamine receptors in freely moving rats. J. Neurosci. 19 (1999) 3594-3609
125. Kojima J., Yamaji Y., Matsumura M., Nambu A., Inase M., Tokuno H., Takada M., and Imai H. Excitotoxic lesions of the pedunculopontine tegmental nucleus produce contralateral hemiparkinsonism in the monkey. Neurosci. Lett. 226 (1997) 111-114
126. Koós T., and Tepper J.M. Inhibitory control of neostriatal projection neurons by GABAergic interneurons. Nat. Neurosci. 2 (1999) 467-472
127. Kreiss D.S., Mastropietro C.W., Rawji S.S., and Walters J.R. The response of subthalamic nucleus neurons to dopamine receptor stimulation in a rodent model of Parkinson's disease. J. Neurosci. 17 (1997) 6807-6819
128. Lavoie B., and Parent A. Pedunculopontine nucleus in the squirrel monkey: projections to the basal ganglia as revealed by anterograde tract-tracing methods. J. Comp. Neurol. 344 (1994) 210-231
129. Lavoie B., Smith Y., and Parent A. Dopaminergic innervation of the basal ganglia in the squirrel monkey as revealed by thyrosine hydroxylase immunohistochemistry. J. Comp. Neurol. 289 (1989) 36-52
130. Leblois A., Boraud T., Meissner W., Bergman H., and Hansel D. Competition between feedback loops underlies normal and pathological dynamics in the basal ganglia. J. Neurosci. 26 (2006) 3567-3583
131. Le Moine C., and Bloch B. D1 and D2 dopamine receptor gene expression in the rat striatum: sensitive cRNA probes demonstrate prominent segregation of D1 and D2 mRNAs in distinct neuronal populations of the dorsal and ventral striatum. J. Comp. Neurol. 355 (1995) 418-426
132. 2 dopamine receptor mRNAs in striatal neurons. Brain Res. 621 (1993) 106-110
133. Lévesque M., and Parent A. The striatofugal fiber system in primates: a reevaluation of its organization based on single-axon tracing studies. Proc. Natl. Acad. Sci. USA 102 (2005) 11888-11893
134. Levine M.S., Li Z., Cepeda C., Cromwell H.C., and Altemus K.L. Neuromodulatory actions of dopamine on synaptically-evoked neostriatal responses in slices. Synapse 24 (1996) 65-78
135. Levy R., Hutchison D., Lozano A.M., and Dostrovsky J.O. High-frequency synchronization of neuronal activity in the subthalamic nucleus of parkinsonian patients with limb tremor. J. Neurosci. 20 (2000) 7766-7775
136. Liu X.-B., and Jones E.G. Predominance of corticothalamic synaptic inputs to thalamic reticular nucleus neurons in the rat. J. Comp. Neurol. 414 (1999) 67-79
137. Lo C.-C., and Wang X.-J. Cortico-basal ganglia circuit mechanism for a decision threshold in reaction time tasks. Nat. Neurosci. 9 (2006) 956-963
138. Lopes da Silva F.H., and Storm van Leeuwen W. The cortical alpha rhythm in dog: the depth and surface profile of phase. In: Brazier M.A.B., and Petsche H. (Eds). Architectonics of the Cerebral Cortex (1978), Raven, New York 319-333
139. Loucif A.J.C., Woodhall G.L., Sehirli U.S., and Stanford I.M. Depolarisation and suppression of burst firing activity in the mouse subthalamic nucleus by dopamine D1/D5 receptor activation of a cyclic-nucleotide gated non-specific cation conductance. Neuropharmacology 55 (2008) 94-105
140. MacLeod N.K., Ryman A., and Arbuthnott G.W. Electrophysiological properties of nigrothalamic neurons after 6-hydroxydopamine lesions in the rat. Neuroscience 38 (1990) 447-456
141. Magill P.J., Bolam J.P., and Bevan M.D. Dopamine regulates the impact of the cerebral cortex on the subthalamic nucleus-globus pallidus network. Neuroscience 106 (2001) 313-330
142. Magnin M., Morel A., and Jeanmonod D. Single-unit analysis of the pallidum, thalamus and subthalamic nucleus in parkinsonian patients. Neuroscience 96 (2000) 549-564
143. Mallet N., Ballion B., Le Moine C., and Gonon F. Cortical inputs and GABA interneurons imbalance projection neurons in the striatum of parkinsonian rats. J. Neurosci. 26 (2006) 3875-3884
144. Maneuf Y.P., Mitchell I.J., Crossman A.R., and Brotchie J.M. On the role of enkephalin cotransmission in the GABAergic striatal efferents to the globus pallidus. Exp. Neurol. 125 (1994) 65-71
145. Maurice N., Deniau J.-M., Glowinski J., and Thierry A.-M. Relationships between the prefrontal cortex and the basal ganglia in the rat: physiology of the corticosubthalamic circuits. J. Neurosci. 18 (1998) 9539-9546
146. McCormick D.A., Connors B.W., Lighthall J.W., and Prince D.A. Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex. J. Neurophysiol. 54 (1985) 782-806
147. McFarland N.R., and Haber S.N. Convergent inputs from thalamic motor nuclei and frontal cortical areas to the dorsal striatum in the primate. J. Neurosci. 20 (2000) 3798-3813
148. Meador-Woodruff J.H., Mansour A., Healy D.J., Kuehn R., Zhou Q.J., Bunzow J.R., Akil H., Civelli O., and Watson Jr. S.J. Comparison of the distributions of D1 and D2 dopamine receptor mRNAs in rat brain. Neuropsychopharmacology 5 (1991) 231-242
149. Merello M., Balej J., Delfino M., Cammarota A., Betti O., and Leiguarda R. Apomorphone induces changes in GPi spontaneous outflow in patients with Parkinson's disease. Mov. Disord. 14 (1999) 45-49
150. Mintz I., Hammond C., and Féger J. Excitatory effect of iontophoretically applied dopamine on identified neurons of the rat subthalamic nucleus. Brain Res. 375 (1986) 172-175
151. Mitchell I.J., Cross A.J., Sambrook M.A., and Crossman A.R. Neural mechanisms mediating 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced parkinsonism in the monkey: relative contributions of the striatopallidal and striatonigral pathways as suggested by 2-deoxyglucose uptake. Neurosci. Lett. 63 (1986) 61-65
152. Miwa H., Nishi K., Fuwa T., and Mizuno Y. Postural effects of unilateral blockade of glutamatergic neurotransmission in the subthalamic nucleus on haloperidol-induced akinesia in rats. Neurosci. Lett. 252 (1998) 167-170
153. Molnar G.F., Pilliar A., Lozano A.M., and Dostrovsky J.O. Differences in neuronal firing rates in pallidal and cerebellar receiving areas of thalamus in patients with Parkinson's disease, essential tremor, and pain. J. Neurophysiol. 93 (2005) 3094-3101
154. Monchi O., Petrides M., Doyon J., Postuma R.B., Worsley K., and Dagher A. Neural bases of set-shifting deficits in Parkinson's disease. J. Neurosci. 24 (2004) 702-710
155. Monchi O., Petrides M., Mejia-Constain B., and Strafella A.P. Cortical activity in Parkinson's disease during executive processing depends on striatal involvement. Brain 130 (2007) 233-244
156. Moyer J.T., Wolf J.A., and Finkel L.H. Effects of dopaminergic modulation on the integrative properties of the ventral striatal medium spiny neuron. J. Neurophysiol. 98 (2007) 3731-3748
157. Nadjar A., Brotchie J.M., Guigoni C., Li Q., Zhou S.-B., Wang G.-J., Ravenscroft P., Georges F., Crossman A.R., and Bezard E. Phenotype of striatofugal medium spiny neurons in parkinsonian and dyskinetic nonhuman primates: a call for a reappraisal of the functional organization of the basal ganglia. J. Neurosci. 26 (2006) 8653-8661
158. Nakanishi H., Kita H., and Kitai S.T. Electrical membrane properties of rat subthalamic neurons in an in vitro slice preparation. Brain Res. 437 (1987) 35-44
159. Nakanishi H., Kita H., and Kitai S.T. Intracellular study of rat entopeduncular nucleus neurons in an in vitro slice preparation: electrical membrane properties. Brain Res. 527 (1990) 81-88
160. Nambu A., and Llinás R. Electrophysiology of globus pallidus neurons in vitro. J. Neurophysiol 72 (1994) 1127-1139
161. Nambu A., and Llinás R. Morphology of globus pallidus neurons: its correlation with electrophysiology in guinea pig brain slices. J. Comp. Neurol. 377 (1997) 85-94
162. Nambu A., Yoshida S., and Jinnai K. Projection on the motor cortex of thalamic neurons with pallidal input in the monkey. Exp. Brain Res. 71 (1988) 658-662
163. Nambu A., Takada M., Inase M., and Tokuno H. Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area. J. Neurosci. 16 (1996) 2671-2683
164. Nambu A., Tokuno H., Inase M., and Takada M. Corticosubthalamic input zones from forelimb representations of the dorsal and ventral divisions of the premotor cortex in the macaque monkey: comparison with the input zones from the primary motor cortex and the supplementary motor area. Neurosci. Lett. 239 (1997) 13-16
165. Nambu A., Tokuno H., Hamada I., Kita H., Imanishi M., Akazawa T., Ikeuchi Y., and Hasegawa N. Excitatory cortical inputs to pallidal neurons via the subthalamic nucleus in the monkey. J. Neurophysiol. 84 (2000) 289-300
166. Ni Z.-G., Bouali-Benazzouz R., Gao D.-M., Benabid A.-L., and Benazzouz A. Time-course of changes in firing rates and firing patterns of subthalamic nucleus neuronal activity after 6-OHDA-induced dopamine depletion in rats. Brain Res. 899 (2001) 142-147
167. Ni Z.-G., Bouali-Benazzouz R., Gao D.-M., Benabid A.-L., and Benazzouz A. Intrasubthalamic injection of 6-hydroxydopamine induces changes in the firing rate and pattern of subthalamic nucleus neurons in the rat. Synapse 40 (2001) 145-153
168. Nicola S.M., and Malenka R.C. Modulation of synaptic transmission by dopamine and norepinephrine in ventral but not dorsal striatum. J. Neurophysiol. 79 (1998) 1768-1776
169. Nicola S.M., Surmeier D.J., and Malenka R.C. Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens. Ann. Rev. Neurosci. 23 (2000) 185-215
170. Nicola S.M., Hopf F.W., and Hjelmstad G.O. Contrast enhancement: a physiological effect of striatal dopamine?. Cell Tissue Res. 318 (2004) 93-106
171. Nowak L.G., and Bullier J. The timing of information transfer in the visual system. In: Rockland K., Kaas J., and Peters A. (Eds). Cerebral Cortex vol. 12 (1997), Plenum Press, New York 205-241
172. Nunez P.L. Wave-like properties of the alpha rhythm. IEEE Trans. Biomed. Eng. 21 (1974) 473-483
173. Nunez P.L. Neocortical Dynamics and Human EEG Rhythms (1995), Oxford University Press, Oxford
174. O'Connor S.C., Robinson P.A., and Chiang A.K.I. Wave-number spectrum of electroencephalographic signals. Phys. Rev. E 66 (2002) 061905.1-061905.12
175. O'Donnell P. Dopamine gating of forebrain neural ensembles. Eur. J. Neurosci. 17 (2003) 429-435
176. Ogura M., and Kita H. Dynorphin exerts both postsynaptic and presynaptic effects in the globus pallidus of the rat. J. Neurophysiol. 83 (2000) 3355-3376
177. Orieux G., François C., Féger J., Yelnik J., Vila M., Ruberg M., Agid Y., and Hirsch E.C. Metabolic activity of excitatory parafascicular and pedunculopontine inputs to the subthalamic nucleus in a rat model of Parkinson's disease. Neuroscience 97 (2000) 79-88
178. Pahapill P.A., and Lozano A.M. The pedunculopontine nucleus and Parkinson's disease. Brain 123 (2000) 1767-1783
179. Palombo E., Porrino L.J., Bankiewicz K.S., Crane A.M., Kopin I.J., and Sokoloff L. Administration of MPTP acutely increase glucose utilization in the substantia nigra of primates. Brain Res. 453 (1988) 227-234
180. Pan H.S., and Walters J.R. Unilateral lesion of the nigrostriatal pathway decreases the firing rate and alters the firing pattern of globus pallidus neurons in the rat. Synapse 2 (1988) 650-656
181. Parent A. Extrinsic connections of the basal ganglia. Trends Neurosci. 13 (1990) 254-258
182. Parent A., and Hazrati L.-N. Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidum in basal ganglia circuitry. Brain Res. Rev. 20 (1995) 128-154
183. Parent A., Smith Y., Filion M., and Dumas J. Distinct afferents to internal and external pallidal segments in the squirrel monkey. Neurosci. Lett. 96 (1989) 140-144
184. Parent M., Levesque M., and Parent A. Two types of projection neurons in the internal pallidum of primates: single-axon tracing and three-dimensional reconstruction. J. Comp. Neurol. 439 (2001) 162-175
185. 33P in situ hybridization study. Neuroscience 88 (1999) 1093-1135
186. Percheron G., Yelnik J., and François C. A Golgi analysis of the primate globus pallidus. III. Spatial organization of the striato-pallidal complex. J. Comp. Neurol. 227 (1984) 214-227
187. Pessiglione M., Guehl D., Rolland A.-S., François C., Hirsch E.C., and Féger J. Thalamic neuronal activity in dopamine-depleted primates: evidence for a loss of functional segregation within basal ganglia circuits. J. Neurosci. 25 (2005) 1523-1531
188. Peters A., and Payne B.R. Numerical relationships between geniculocortical afferents and pyramidal cell modules in cat primary visual cortex. Cereb. Cortex 3 (1993) 69-78
189. Plenz D. When inhibition goes incognito: feedback interaction between spiny projection neurons in striatal function. Trends Neurosci. 26 (2003) 436-443
190. Prechtl J.C., Cohen L.B., Pesaran B., Mitra P.P., and Kleinfeld D. Visual stimuli induce waves of electrical activity in turtle cortex. Proc. Natl. Acad. Sci. USA 94 (1997) 7621-7626
191. 2 dopamine receptors control globus pallidus neurons activity in the rat. Neurosci. Lett. 300 (2001) 79-82
192. Raeva S.N., and Lukashev A.O. Characteristics of background unit activity in the nucleus reticularis of the human thalamus. Neurophysiology 19 (1987) 335-343
193. Ragsdale Jr. C.W., and Graybiel A.M. Multiple patterns of striatal innervation in the cat. In: Bentivoglio M., and Spreafico R. (Eds). Cellular Thalamic Mechanisms (1988), Elsevier, Amsterdam 261-267
194. Raynor K., Kong H., Mestek A., Bye L.S., Tian M., Liu J., Yu L., and Reisine T. Characterization of the cloned human mu opioid receptor. J. Pharmacol. Exp. Ther. 272 (1995) 423-428
195. Reiner A., Albin R.L., Anderson K.D., D'Amato C.J., Penney J.B., and Young A.B. Differential loss of striatal projections neurons in Huntington's disease. Proc. Natl. Acad. Sci. USA 85 (1988) 5733-5737
196. Rennie C.J., Robinson P.A., and Wright J.J. Effects of local feedback on dispersion of electrical waves in the cerebral cortex. Phys. Rev. E 59 (1999) 3320-3329
197. Rennie C.J., Wright J.J., and Robinson P.A. Mechanisms of cortical electrical activity and emergence of gamma rhythm. J. Theor. Biol. 205 (2000) 17-35
198. Ridding M.C., Inzelberg R., and Rothwell J.C. Changes in excitability of motor cortical circuitry in patients with Parkinson's disease. Ann. Neurol. 37 (1995) 181-188
199. Roberts J.A., and Robinson P.A. Modeling absence seizure dynamics: implications for basic mechanisms and measurement of thalamocortical and corticothalamic latencies. J. Theor. Biol. 253 (2008) 189-201
200. Robinson P.A. Neurophysical theory of coherence and correlations of electroencephalographic signals. J. Theor. Biol. 222 (2003) 163-175
201. Robinson P.A., Rennie C.J., and Wright J.J. Propagation and stability of waves of electrical activity in the cerebral cortex. Phys. Rev. E 56 1 (1997) 826-840
202. Robinson P.A., Rennie C.J., Wright J.J., Bahramali H., Gordon E., and Rowe D.L. Prediction of electroencephalographic spectra from neurophysiology. Phys. Rev. E 63 (2001) 021903.1-021903.18
203. Robinson P.A., Loxley P.N., O'Connor S.C., and Rennie C.J. Modal analysis of corticothalamic dynamics, electroencephalographic spectra, and evoked potentials. Phys. Rev. E 63 (2001) 041909.1-041909.13
204. Robinson P.A., Rennie C.J., and Rowe D.L. Dynamics of large-scale brain activity in normal arousal states and epileptic seizures. Phys. Rev. E 65 (2002) 041924.1-041924.9
205. Robinson P.A., Rennie C.J., Rowe D.L., O'Connor S.C., Wright J.J., Gordon E., and Whitehouse R.W. Neurophysical modeling of brain dynamics. Neuropsychopharmacology 28 Suppl. 1 (2003) 74-79
206. Robinson P.A., Rennie C.J., Rowe D.L., and O'Connor S.C. Estimation of multiscale neurophysiologic parameters by electroencephalographic means. Hum. Brain Mapp. 23 (2004) 53-72
207. Robinson P.A., Rennie C.J., Rowe D.L., O'Connor S.C., and Gordon E. Multiscale brain modelling. Phil. Trans. R. Soc. B 360 (2005) 1043-1050
208. Robledo P., and Feger J. Acute monoaminergic depletion in the rat potentiates the excitatory effect of the subthalamic nucleus in the substantia nigra pars reticulata but not in the pallidal complex. J. Neural Transm. 86 (1991) 115-126
209. Rohlfs A., Nikkah G., Rosenthal C., Rundfeldt C., Brandis A., Samii M., and Löscher W. Hemispheric asymmetries in spontaneous firing characteristics of substantia nigra pars reticulata neurons following a unilateral 6-hydroxydopamine lesion of the rat nigrostriatal pathway. Brain Res. 761 (1997) 352-356
210. Rolland A.-S., Herrero M.-T., Garcia-Martinez V., Ruberg M., Hirsch E.C., and François C. Metabolic activity of cerebellar and basal ganglia-thalamic neurons is reduced in parkinsonism. Brain 130 (2007) 265-275
211. Rowe D.L., Robinson P.A., and Rennie C.J. Estimation of neurophysiological parameters from the waking EEG using a biophysical model of brain dynamics. J. Theor Biol. 231 (2004) 413-433
212. Rubin J.E., and Terman D. High frequency stimulation of the subthalamic nucleus eliminates pathological thalamic rhythmicity in a computational model. J. Comp. Neurosci. 16 (2004) 211-235
213. Rubino D., Robbins K.A., and Hatsopoulos N.G. Propagating waves mediate information transfer in the motor cortex. Nat. Neurosci. 9 (2006) 1549-1557
214. Sadikot A.F., Parent A., Smith Y., and Bolam J.P. Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: a light and election microscopic study of the thalamostriatal projection in relations to striatal heterogeneity. J. Comp. Neurol. 320 (1992) 228-242
215. Salenius S., Avikainen S., Kaakola S., Hari R., and Brown P. Defective cortical drive to muscle in Parkinson's disease and its improvement with levodopa. Brain 125 (2002) 491-500
216. Sato F., Lavallée P., Lévesque M., and Parent A. Single-axon tracing study of neurons of the external segment of the globus pallidus in primate. J. Comp. Neurol. 417 (2000) 17-31
217. Schiff S.J., Huang X., and Wu J.-Y. Dynamical evolution of spatiotemporal patterns in mammalian middle cortex. Phys. Rev. Lett. 98 (2007) 178102.1-178102.4
218. Schneider J.S., and Rothblat D.S. Alterations in intralaminar and motor thalamic physiology following nigrostriatal dopamine depletion. Brain Res. 742 (1996) 25-33
219. Schultz W. Activity of pars reticulata neurons of monkey substantia nigra in relation to motor, sensory, and complex events. J. Neurophysiol. 55 (1986) 660-677
220. Sesack S.R., and Bunney B.S. Pharmacological characterization of the receptor mediating electrophysiological responses to dopamine in the rat medial prefrontal cortex: a microiontophoretic study. J. Pharmacol. Exp. Ther. 248 (1989) 1323-1333
221. Shen K.-.Z., and Johnson S.W. Presynaptic modulation of synaptic transmission by opioid receptor in rat subthalamic nucleus in vitro. J. Physiol. 541 (2002) 219-230
222. Sherman S.M., and Guillery R.W. The role of the thalamus in the flow of information to the cortex. Phil. Trans. R. Soc. London B 357 (2002) 1695-1708
223. Shink E., and Smith Y. Differential synaptic innervation of neurons in the internal and external segments of the globus pallidus by the GABA- and glutamate-containing terminals in the squirrel monkey. J. Comp. Neurol. 358 (1995) 119-141
224. Shink E., Bevan M.D., Bolam J.P., and Smith Y. The subthalamic nucleus and the external pallidum: two tightly interconnected structures that control the output of the basal ganglia in the monkey. Neuroscience 73 (1996) 335-357
225. Sidibé M., and Smith Y. Differential synaptic innervation of striatofugal neurones projecting to the internal or external segments of the globus pallidus by thalamic afferents in the squirrel monkey. J. Comp. Neurol. 365 (1996) 445-465
226. Smith Y., Lavoie B., Dumas J., and Parent A. Evidence for a distinct nigropallidal dopaminergic projection in the squirrel monkey. Brain Res. 482 (1989) 381-386
227. Smith Y., Bolam J.P., and Von Krosigk M. Topographical and synaptic organization of the GABA-containing pallidosubthalamic projection in the rat. Eur. J. Neurosci. 2 (1990) 500-511
228. Smith Y., Hazrati L.-N., and Parent A. Efferent projections of the subthalamic nucleus in the squirrel monkey as studies by the PHA-L anterograde tracing method. J. Comp. Neurol. 294 (1990) 306-323
229. Smith Y., Wichmann T., and DeLong M.R. Synaptic innervation of neurones in the internal pallidal segment by the subthalamic nucleus and the external pallidum in monkeys. J. Comp. Neurol. 343 (1994) 297-318
230. A IPSCs in the rat globus pallidus in vitro. J. Neurosci. 19 (1999) 4796-4803
231. Steiner H., and Gerfen C.R. Role of dynorphin and enkephalin in the regulation of striatal output pathways and behavior. Exp. Brain Res. 123 (1998) 60-76
232. Steriade M. The GABAergic reticular nucleus: a preferential target of corticothalamic projections. Proc. Natl. Acad. Sci. USA 98 (2001) 3625-3627
233. Steriade M., Domich L., and Oakson G. Reticularis thalami neurons revisited: activity changes during shifts in states of vigilance. J. Neurosci. 6 (1986) 68-81
234. Steriade M., Timofeev I., Dürmüller N., and Grenier F. Dynamic properties of corticothalamic neurons and local cortical interneurons generating fast rhythmic (30-40 Hz) spike bursts. J. Neurophysiol. 79 (1998) 483-490
235. Steriade M., Timofeev I., and Grenier F. Natural waking and sleep states: a view from inside neocortical neurons. J. Neurophysiol. 85 (2001) 1969-1985
236. Sterio D., Berić A., Dogali M., Fazzini E., Alfaro G., and Devinsky O. Neurophysiological properties of pallidal neurons in Parkinson's disease. Ann. Neurol. 35 (1994) 586-591
237. Strauss U., Zhou F.-W., Henning J., Battefeld A., Wree A., Köhling R., Haas S.J.-P., Benecke R., Rolfs A., and Gimsa U. Increasing extracellular potassium results in subthalamic neuron activity resembling that seen in a 6-hydroxydopamine lesion. J. Neurophysiol. 99 (2008) 2902-2915
238. Strick P.L., Dum R.P., and Picard N. Macro-organization of the circuits connecting the basal ganglia with the cortical motor areas. In: Houk J., Davis J., and Beiser D. (Eds). Models of Information Processing in the Basal Ganglia (1995), MIT Press, Cambridge, MA 117-130
239. Surmeier D.J., Eberwine J., Wilson C.J., Cao Y., Stefani A., and Kitai S.T. Dopamine receptor subtypes colocalize in rat striatonigral neurons. Proc. Natl. Acad. Sci. USA 89 (1992) 10178-10182
240. Surmeier D.J., Song W.-J., and Yan Z. Coordinated expression of dopamine receptors in neostriatal medium spiny neurons. J. Neurosci. 16 (1996) 6579-6591
241. Swerdlow N.R., and Koob G.F. Dopamine, schizophrenia, mania and depression-toward a unified hypothesis of cortico-striato-pallido-thalamic function. Behav. Brain Sci. 10 (1987) 197-207
242. Taverna S., van Dongen Y.C., Groenewegen H.J., and Pennartz C.M.A. Direct physiological evidence for synaptic connectivity between medium-sized spiny neurons in rat nucleus accumbens in situ. J. Neurophysiol. 91 (2004) 1111-1121
243. Terman D., Rubin J.E., Yew A.C., and Wilson C.J. Activity patterns in a model for the subthalamopallidal network of the basal ganglia. J. Neurosci. 22 (2002) 2963-2976
244. Thomson A.M. Activity-dependent properties of synaptic transmission at two classes of connections made by rat neocortical pyramidal axons in vitro. J. Physiol. 502 (1997) 131-147
245. Thurley K., Senn W., and Lüscher H.-R. Dopamine increases the gain of the input-output response of rat prefrontal pyramidal neurons. J. Neurophysiol. 99 (2008) 2985-2997
246. Toan D.L., and Schultz W. Responses of rat pallidum cells to cortex stimulation and effects of altered dopaminergic activity. Neuroscience 15 (1985) 683-694
247. Tseng K.Y., Kasanetz F., Kargieman L., Riquelme L.A., and Murer M.G. Cortical slow oscillatory activity is reflected in the membrane potential and spike trains of striatal neurons in rats with chronic nigrostriatal lesions. J. Neurosci. 21 (2001) 6430-6439
248. Turner J.P., and Salt T.E. Characterization of sensory and corticothalamic excitatory inputs to rat thalamocortical neurones in vitro. J. Physiol. 510 (1998) 829-843
249. Umemiya M., and Raymond L.A. Dopaminergic modulation of excitatory postsynaptic currents in rat neostriatal neurons. J. Neurophysiol. 78 (1997) 1248-1255
250. Ungerstedt U. 6-hydroxy-dopamine induced degeneration of central monoamine neurons. Eur. J. Pharmacol. 5 (1968) 107-110
251. Uno M., Ozawa N., and Yoshida M. The mode of pallido-thalamic transmission investigated with intracellular recording from cat thalamus. Exp. Brain Res. 33 (1978) 493-507
252. Van Albada, S.J., Gray, R.T., Drysdale, P.M., Robinson, P.A., 2009. Mean-field modeling of the basal ganglia-thalamocortical system. II. Dynamics of electrophysiological changes in Parkinson's disease. J. Theor. Biol., in press, 10.1016/j.jtbi.2008.12.013.
253. Voloshin M.Y., and Prokopenko V.F. Neuronal responses of the reticular and anterior ventral thalamic nuclei to stimulation of the thalamic ventrolateral nucleus and motor cortex. Neurophysiology 10 (1978) 336-342
254. Walker F.O. Huntington's disease. Lancet 369 (2007) 218-228
255. Walters J.R., Hu D., Itoga C.A., Parr-Brownlie L.C., and Bergstrom D.A. Phase relationships support a role for coordinated activity in the indirect pathway in organizing slow oscillations in basal ganglia output after loss of dopamine. Neuroscience 144 (2007) 762-776
256. Wannier T.M.J., Maier M.A., and Hepp-Reymond M.-C. Contrasting properties of monkey somatosensory and motor cortex neurons activated during the control of force in precision grip. J. Neurophysiol. 65 (1991) 572-589
257. Waters C.M., Peck R., Rossor M., Reynolds G.P., and Hunt S.P. Immunocytochemical studies on the basal ganglia and substantia nigra in Parkinson's disease and Huntington's chorea. Neuroscience 25 (1988) 419-438
258. Wichmann T., Bergman H., Starr P.A., Subramanian T., Watts R.L., and DeLong M.R. Comparison of MPTP-induced changes in spontaneous neuronal discharge in the internal pallidal segment and in the substantia nigra pars reticulata in primates. Exp. Brain Res. 125 (1999) 397-409
259. Williams S.M., and Goldman-Rakic P.S. Characterization of the dopaminergic innervation of the primate cortex using a dopamine-specific antibody. Cereb. Cortex 3 (1993) 199-222
260. Wilson C.J. The contribution of cortical neurons to the firing pattern of striatal spiny neurons. In: Houk J., Davis J., and Beiser D. (Eds). Models of Information Processing in the Basal Ganglia (1995), MIT Press, Cambridge, MA 29-50
261. Wright J.J., and Liley D.T.J. Simulation of electrocortical waves. Biol. Cybern. 72 (1995) 347-356
262. Wu J.-Y., Guan L., and Tsau Y. Propagating activation during oscillations and evoked responses in neocortical slices. J. Neurosci. 19 (1999) 5005-5015
263. Wu Y., Richard S., and Parent A. The organization of the striatal output system: a single-cell juxtacellular labeling study in the rat. Neurosci. Res. 38 (2000) 49-62
264. Xu W., Huang X., Takagaki K., and Wu J.-Y. Compression and reflection of visually evoked cortical waves. Neuron 55 (2007) 119-129
265. Yelnik J. Functional anatomy of the basal ganglia. Mov. Disord. 17 Suppl. 3 (2002) S15-S21
266. Yelnik J., François C., Percheron G., and Tandé D. Morphological taxonomy of the neurons of the primate striatum. J. Comp. Neurol. 313 (1991) 273-294
267. Yoshida M. The neuronal mechanism underlying parkinsonism and dyskinesia: differential roles of the putamen and caudate nucleus. Neurosci. Res. 12 1 (1991) 31-40
268. Yoshida S., Nambu A., and Jinnai K. The distribution of the globus pallidus neurons with input from various cortical areas in the monkeys. Brain. Res. 611 (1993) 170-174
269. Zhou F.-M., and Hablitz J.J. Dopamine modulation of membrane and synaptic properties of interneurons in rat cerebral cortex. J. Neurophysiol. 81 (1999) 967-976
270. Zhu Z.T., Bartol M., Shen K.Z., and Johnson S.W. Excitatory effects of dopamine on subthalamic nucleus neurons: in vitro study of rats pretreated with 6-hydroxydopamine and levodopa. Brain Res. 945 (2002) 31-40
271. Zweig R.M., Jankel W.R., Hedreen J.C., Mayeux R., and Price D.L. The pedunculopontine nucleus in Parkinson's disease. Ann. Neurol. 26 (1989) 41-46